The University of Queensland

Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism

Johnson, S. R., Leo, P. J., McInerney-Leo, A. M., Anderson, L. K., Marshall, M., McGown, I., Newell, F., Brown, M. A., Conwell, L. S., Harris, M. and Duncan, E. L. (2018). Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism. Pediatric Diabetes, 19 (4), 656-662. doi: 10.1111/pedi.12638

Insulin regimens for newly diagnosed children with type 1 diabetes in Australia and New Zealand: a survey of current practice

Selvakumar, Dharrsinee, Al-Sallami, Heshan S., de Bock, Martin, Ambler, Geoffrey R., Benitez-Aguirre, Paul, Wiltshire, Esko, Tham, Elaine, Simm, Peter, Conwell, Louise S., Carter, Phillipa J., Willis, Jinny, Wheeler, Benjamin J. and PSNZ Diabetes Clinical Network (2017). Insulin regimens for newly diagnosed children with type 1 diabetes in Australia and New Zealand: a survey of current practice. Journal of Paediatrics and Child Health, 53 (12), 1208-1214. doi: 10.1111/jpc.13631

Functional characterization of multiple DICER1 mutations in an adolescent

Wu, M. K., de Kock, L., Conwell, L. S., Stewart, C. J. R., King, B. R., Choong, C. S., Hussain, K., Sabbaghian, N., MacRae, I. J., Fabian, M. R. and Foulkes, W. D. (2016). Functional characterization of multiple DICER1 mutations in an adolescent. Endocrine-Related Cancer, 23 (2), L1-L5. doi: 10.1530/ERC-15-0460

18Fluoro-dihydroxy phenylalanine positron emission tomography/computed tomography scanning for congenital hyperinsulinism of infancy

Conwell, Louise S., Greer, Ristan M., Neville, Kristen A., Amato, Lisa A., Campbell, Louise and Fiumara, Frank (2015). 18Fluoro-dihydroxy phenylalanine positron emission tomography/computed tomography scanning for congenital hyperinsulinism of infancy. Journal of Paediatrics and Child Health, 51 (8), 826-829. doi: 10.1111/jpc.12827

Bisphosphonates for osteoporosis in people with cystic fibrosis (Review)

Conwell, Louise S. and Chang, Anne B. (2014). Bisphosphonates for osteoporosis in people with cystic fibrosis (Review). Cochrane Database of Systematic Review, 2014 (3) CD002010. doi: 10.1002/14651858.CD002010.pub4

Probiotics for preventing gestational diabetes (Review)

Barrett, Helen L., Nitert, Marloes Dekker, Conwell, Louise S. and Callaway, Leonie K. (2014). Probiotics for preventing gestational diabetes (Review). Cochrane Database of Systematic Reviews, 2014 (2) CD009951. doi: 10.1002/14651858.CD009951.pub2

Probiotics for preventing gestational diabetes (Protocol)

Barrett, Helen L., Nitert, Marloes Dekker, Conwell, Louise S. and Callaway, Leonie K. (2012). Probiotics for preventing gestational diabetes (Protocol). Cochrane Database of Systematic Review (7 ). doi: 10.1002/14651858.CD009951

[18F]-DOPA PET/CT Imaging in Congenital Hyperinsulinism - First 12 months of the Australian experience.

Conwell, L. S., Greer, R. M., Walker, R. M., Fiumara, F., Campbell, L., Harris, M. and Cotterill, A. M. (2012). [18F]-DOPA PET/CT Imaging in Congenital Hyperinsulinism - First 12 months of the Australian experience.. Monogenic Disorders of Insulin Secretion: Congenital Hyperinsulinism and Neonatal Disorders, Philadelphia Pennsylvania, 15-16 March 2012. Malden, MA, United States: Wiley-Blackwell Publishing. doi: 10.1111/j.1399-5448.2012.00887.x

Hypothalamic obesity following craniopharyngioma surgery: results of a pilot trial of combined metformin and diazoxide therapy

Hamilton, Jill K., Conwell, Louise S., Syme, Catriona, Ahmet, Alexandra, Jefferies, Allison and Daneman, Denis (2011). Hypothalamic obesity following craniopharyngioma surgery: results of a pilot trial of combined metformin and diazoxide therapy. International Journal of Pediatric Endocrinology, 2011 (1). doi: 10.1155/2011/417949

Considering statins for cholesterol-reduction in children if lifestyle and diet changes do not improve their health: A review of the risks and benefits

O’Gorman, Clodagh S.M., O’Neill, Michael B. and Conwell, Louise S. (2011). Considering statins for cholesterol-reduction in children if lifestyle and diet changes do not improve their health: A review of the risks and benefits. Vascular Health and Risk Management, 7 (1), 1-14. doi: 10.2147/VHRM.S7356

Klebsiella pneumoniae bacteraemia complicating rotavirus gastroenteritis in two infants with glucocorticoid deficiency

Longmore, DK, Batch, JA, McMahon, SK and Conwell, LS (2010). Klebsiella pneumoniae bacteraemia complicating rotavirus gastroenteritis in two infants with glucocorticoid deficiency. Journal of Pediatric Endocrinology and Metabolism, 23 (3), 293-295. doi: 10.1515/JPEM.2010.23.3.293

The feasibility of a home-based moderate-intensity physical activity intervention in obese children and adolescents

Conwell, Louise S., Trost, Stewart G., Spence, Luke, Brown, Wendy J. and Batch, Jennifer A. (2010). The feasibility of a home-based moderate-intensity physical activity intervention in obese children and adolescents. British Journal of Sports Medicine, 44 (4), 250-255. doi: 10.1136/bjsm.2008.046359

Dermatological Complications of Continuous Subcutaneous Insulin Infusion in Children and Adolescents

Conwell, Louise S., Pope, Elena, Artiles, Ana M., Mohanta, Arun, Daneman, Alan and Daneman, Denis (2008). Dermatological Complications of Continuous Subcutaneous Insulin Infusion in Children and Adolescents. The Journal of Pediatrics, 152 (5), 622-628. doi: 10.1016/j.jpeds.2007.10.006

Necrotizing fasciitis in adolescents with poorly controlled type 1 diabetes mellitus: report of two cases

Conwell, Louise S., Forrest, Christopher R., Allen, Upton D., Perlman, Kusiel and Daneman, Denis (2007). Necrotizing fasciitis in adolescents with poorly controlled type 1 diabetes mellitus: report of two cases. Pediatric diabetes, 8 (6), 397-400. doi: 10.1111/j.1399-5448.2007.00244.x

Oral glucose tolerance test in children and adolescents: Positives and pitfalls

Conwell, L. S. and Batch, J. A. (2004). Oral glucose tolerance test in children and adolescents: Positives and pitfalls. Journal of Paediatrics And Child Health, 40 (11), 620-626. doi: 10.1111/j.1440-1754.2004.00487.x

Infertility and pregnancy issues

Conwell, L.S. and Foong, S. (2008). Infertility and pregnancy issues. Turner Syndrome Across the Lifespan. edited by Jill Hamilton and Irena Hozjan. Ontario, Canada: Charterhouse Publishing.

Blood pressure in adolescents and young adults with type 1 diabetes: data from the Australasian Diabetes Data Network registry

James, Steven, Perry, Lin, Lowe, Julia, Harris, Margaret, Colman, Peter G., Craig, Maria E., Anderson, Kym, Andrikopoulos, Sof, Ambler, Geoff, Barrett, Helen, Batch, Jenny, Bergman, Philip, Cameron, Fergus, Conwell, Louise, Cotterill, Andrew, Cooper, Chris, Couper, Jennifer, Davis, Elizabeth, de Bock, Martin, Donaghue, Kim, Fairchild, Jan, Fegan, Gerry, Fourlanos, Spiros, Glastras, Sarah, Goss, Peter, Gray, Leonie, Hamblin, Peter Shane, Hofman, Paul, Holmes-Walker, Dianne Jane ... Zimmermann, Anthony (2023). Blood pressure in adolescents and young adults with type 1 diabetes: data from the Australasian Diabetes Data Network registry. Acta Diabetologica, 60 (6), 797-803. doi: 10.1007/s00592-023-02057-4

Bisphosphonates for osteoporosis in people with cystic fibrosis

Jeffery, Tomas C, Chang, Anne B and Conwell, Louise S (2023). Bisphosphonates for osteoporosis in people with cystic fibrosis. Cochrane Database of Systematic Reviews, 2023 (1) CD002010. doi: 10.1002/14651858.cd002010.pub5

Improved local diagnosis of focal hyperinsulinism in the COVID‐19 era by interstate radiopharmaceutical transport

Vanderniet, Joel, Neville, Kristen A., Conwell, Louise S., Wegner, Eva A., Craig, Maria E., Adams, Susan, Gifford, Andrew J., Koutsiofi, Melissa, Calabria, Frances M., Maguire, Gemma, Thomas, Paul, Campbell, Louise and Woodhead, Helen J. (2022). Improved local diagnosis of focal hyperinsulinism in the COVID‐19 era by interstate radiopharmaceutical transport. Journal of Paediatrics and Child Health, 59 (2), 398-400. doi: 10.1111/jpc.16307

Suboptimal glycemic control in adolescents and young adults with type 1 diabetes from 2011 to 2020 across Australia and New Zealand: data from the Australasian Diabetes Data Network registry

James, Steven, Perry, Lin, Lowe, Julia, Harris, Margaret, Craig, Maria E., Anderson, Kym, Andrikopoulos, Sof, Ambler, Geoff, Barrett, Helen, Batch, Jenny, Bergman, Philip, Cameron, Fergus, Colman, Peter, Conwell, Louise, Cotterill, Andrew, Cooper, Chris, Couper, Jennifer, Davis, Elizabeth, de Bock, Martin, Donaghue, Kim, Fairchild, Jan, Fegan, Gerry, Fourlanos, Spiros, Glastras, Sarah, Gray, Leonie, Hamblin, Shane, Hofman, Paul, Holmes-Walker, Dianne Jane, Howard, Neville ... Zimmermann, Anthony (2022). Suboptimal glycemic control in adolescents and young adults with type 1 diabetes from 2011 to 2020 across Australia and New Zealand: data from the Australasian Diabetes Data Network registry. Pediatric Diabetes, 23 (6), 736-741. doi: 10.1111/pedi.13364

Type 2 diabetes in children and adolescents across Australia and New Zealand: A 6-year audit from The Australasian Diabetes Data Network (ADDN)

Ludwig, Karissa, Craig, Maria E., Donaghue, Kim C., Maguire, Ann, Benitez-Aguirre, Paul Z., Colman, Peter, Craig, Maria, Jones, Tim, Sinnott, Richard, Ambler, Geoff, Barrett, Helen, Batch, Jenny, Bergman, Philip, Cameron, Fergus, Conwell, Louise, Cotterill, Andrew, Couper, Jennifer, Davis, Elizabeth, Donaghue, Kim, Fairchild, Jan, Fegan, Gerry, Gray, Leonie, Hamblin, Shane, Hofman, Paul, Holmes–Walker, Jane, Howard, Neville, Jack, Michelle, James, Steven, Jefferies, Craig ... Zoungas, Sophia (2021). Type 2 diabetes in children and adolescents across Australia and New Zealand: A 6-year audit from The Australasian Diabetes Data Network (ADDN). Pediatric Diabetes, 22 (3), 380-387. doi: 10.1111/pedi.13169

Hypophosphataemic rickets: the long and short of it

Musthaffa, Yassmin and Conwell, Louise S . (2020). Hypophosphataemic rickets: the long and short of it. Journal of Paediatrics and Child Health, 57 (9) jpc.15277, 1519-1523. doi: 10.1111/jpc.15277

Challenges of managing congenital hyperinsulinism in remote Aboriginal Australian communities

Musthaffa, Yassmin, Papadimos, Emily R., Fairchild, Jan, Titmuss, Angela, Corpus, Sumaria, Huynh, Tony and Conwell, Louise S. (2020). Challenges of managing congenital hyperinsulinism in remote Aboriginal Australian communities. Journal of Paediatrics and Child Health, 57 (5) jpc.14984, 727-731. doi: 10.1111/jpc.14984

Response to Comment on Johnson et al. Cost-effectiveness analysis of routine screening using massively parallel sequencing for maturity-onset diabetes of the young in a pediatric diabetes cohort: reduced health system costs and improved patient quality of life. Diabetes Care 2019;42:69–76

Johnson, Stephanie R., Carter, Hannah E., Leo, Paul, Hollingworth, Samantha A., Davis, Elizabeth A., Jones, Timothy W., Conwell, Louise S., Harris, Mark, Brown, Matthew A., Graves, Nicholas and Duncan, Emma L. (2019). Response to Comment on Johnson et al. Cost-effectiveness analysis of routine screening using massively parallel sequencing for maturity-onset diabetes of the young in a pediatric diabetes cohort: reduced health system costs and improved patient quality of life. Diabetes Care 2019;42:69–76. Diabetes Care, 42 (5), e79-e80. doi: 10.2337/dci19-0010

Comprehensive genetic screening: the prevalence of MODY gene variants in a population-based childhood diabetes cohort

Johnson, Stephanie R., Ellis, Jonathan J., Leo, Paul, Anderson, Lisa K., Ganti, Uma, Harris, Jessica E., Curran, Jacqueline A., McInerney-Leo, Aideen, Paramalingam, Nirubasini, Song, Xiaoxia, Conwell, Louise S., Harris, Mark, Jones, Timothy W., Brown, Matthew A., Davis, Elizabeth A. and Duncan, Emma L. (2019). Comprehensive genetic screening: the prevalence of MODY gene variants in a population-based childhood diabetes cohort. Pediatric Diabetes, 20 (1), 57-64. doi: 10.1111/pedi.12766

Autonomous thyroid nodule: not just a disease of adulthood

Papadimos, Emily R., Perry, Emily, Goodwin, Bruce and Conwell, Louise S. (2019). Autonomous thyroid nodule: not just a disease of adulthood. Journal of Paediatrics and Child Health, 56 (7) jpc.14734, 1140-1143. doi: 10.1111/jpc.14734

Cost-effectiveness analysis of routine screening using massively parallel sequencing for maturity-onset diabetes of the young in a pediatric diabetes cohort: reduced health system costs and improved patient quality of life

Johnson, Stephanie R., Carter, Hannah E., Leo, Paul, Hollingworth, Samantha A., Davis, Elizabeth A., Jones, Timothy W., Conwell, Louise S., Harris, Mark, Brown, Matthew A., Graves, Nicholas and Duncan, Emma L. (2019). Cost-effectiveness analysis of routine screening using massively parallel sequencing for maturity-onset diabetes of the young in a pediatric diabetes cohort: reduced health system costs and improved patient quality of life. Diabetes Care, 42 (1), 69-76. doi: 10.2337/dc18-0261

Predicted benign and synonymous variants in CYP11A1 causes primary adrenal insufficiency through missplicing

Maharaj, Avinaash, Buonocore, Federica, Meimaridou, Eirini, Ruiz-Babot, Gerard, Guasti, Leonardo, Peng, Hwei-Ming, Capper, Cameron P., Burgos-Tirado, Neikelyn, Prasad, Rathi, Hughes, Claire R., Maudhoo, Ashwini, Crowne, Elizabeth, Cheetham, Timothy D., Brain, Caroline E., Suntharalingham, Jenifer P., Striglioni, Niccolò, Yuksel, Bilgin, Gurbuz, Fatih, Gupta, Sangay, Lindsay, Robert, Couch, Robert, Spoudeas, Helen A., Guran, Tulay, Johnson, Stephanie, Fowler, Dallas J, Conwell, Louise S., McInerney-Leo, Aideen M., Drui, Delphine, Cariou, Bertrand ... Metherell, Louise A. (2018). Predicted benign and synonymous variants in CYP11A1 causes primary adrenal insufficiency through missplicing. Journal of the Endocrine Society, 3 (1), 201-221. doi: 10.1210/js.2018-00130

Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY): a novel ABCC8 mutation in a previously screened family

Johnson, Stephanie R., Leo, Paul, Conwell, Louise S., Harris, Mark, Brown, Matthew A. and Duncan, Emma L. (2018). Clinical usefulness of comprehensive genetic screening in maturity onset diabetes of the young (MODY): a novel ABCC8 mutation in a previously screened family. Journal of Diabetes, 10 (9), 764-767. doi: 10.1111/1753-0407.12778

Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism

Johnson, S. R., Leo, P. J., McInerney-Leo, A. M., Anderson, L. K., Marshall, M., McGown, I., Newell, F., Brown, M. A., Conwell, L. S., Harris, M. and Duncan, E. L. (2018). Whole-exome sequencing for mutation detection in pediatric disorders of insulin secretion: Maturity onset diabetes of the young and congenital hyperinsulinism. Pediatric Diabetes, 19 (4), 656-662. doi: 10.1111/pedi.12638

A novel INS mutation in a family with maturity-onset diabetes of the young: variable insulin secretion and putative mechanisms

Johnson, Stephanie R., Mcgown, Ivan, Oppermann, Udo, Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2018). A novel INS mutation in a family with maturity-onset diabetes of the young: variable insulin secretion and putative mechanisms. Pediatric Diabetes, 19 (5), 905-909. doi: 10.1111/pedi.12679

Insulin regimens for newly diagnosed children with type 1 diabetes in Australia and New Zealand: a survey of current practice

Selvakumar, Dharrsinee, Al-Sallami, Heshan S., de Bock, Martin, Ambler, Geoffrey R., Benitez-Aguirre, Paul, Wiltshire, Esko, Tham, Elaine, Simm, Peter, Conwell, Louise S., Carter, Phillipa J., Willis, Jinny, Wheeler, Benjamin J. and PSNZ Diabetes Clinical Network (2017). Insulin regimens for newly diagnosed children with type 1 diabetes in Australia and New Zealand: a survey of current practice. Journal of Paediatrics and Child Health, 53 (12), 1208-1214. doi: 10.1111/jpc.13631

Functional characterization of multiple DICER1 mutations in an adolescent

Wu, M. K., de Kock, L., Conwell, L. S., Stewart, C. J. R., King, B. R., Choong, C. S., Hussain, K., Sabbaghian, N., MacRae, I. J., Fabian, M. R. and Foulkes, W. D. (2016). Functional characterization of multiple DICER1 mutations in an adolescent. Endocrine-Related Cancer, 23 (2), L1-L5. doi: 10.1530/ERC-15-0460

Allan-Herndon-Dudley syndrome with unusual profound sensorineural hearing loss

Gagliardi, Lucia, Nataren, Nathalie, Feng, Jinghua, Schreiber, Andreas W., Hahn, Christopher N., Conwell, Louise S., Coman, David and Scott, Hamish S. (2015). Allan-Herndon-Dudley syndrome with unusual profound sensorineural hearing loss. American Journal of Medical Genetics, Part A, 167 (8), 1872-1876. doi: 10.1002/ajmg.a.37075

Relation of reduced preclinical left ventricular diastolic function and cardiac remodeling in overweight youth to insulin resistance and inflammation

Dahiya, Rachana, Shultz, Sarah P., Dahiya, Arun, Fu, Jinlin, Flatley, Christopher, Duncan, Danusia, Cardinal, John, Kostner, Karam M., Byrne, Nuala M., Hills, Andrew P., Harris, Mark, Conwell, Louise S. and Leong, Gary M. (2015). Relation of reduced preclinical left ventricular diastolic function and cardiac remodeling in overweight youth to insulin resistance and inflammation. American Journal of Cardiology, 115 (9), 1222-1228. doi: 10.1016/j.amjcard.2015.02.005

18Fluoro-dihydroxy phenylalanine positron emission tomography/computed tomography scanning for congenital hyperinsulinism of infancy

Conwell, Louise S., Greer, Ristan M., Neville, Kristen A., Amato, Lisa A., Campbell, Louise and Fiumara, Frank (2015). 18Fluoro-dihydroxy phenylalanine positron emission tomography/computed tomography scanning for congenital hyperinsulinism of infancy. Journal of Paediatrics and Child Health, 51 (8), 826-829. doi: 10.1111/jpc.12827

Bisphosphonates for osteoporosis in people with cystic fibrosis (Review)

Conwell, Louise S. and Chang, Anne B. (2014). Bisphosphonates for osteoporosis in people with cystic fibrosis (Review). Cochrane Database of Systematic Review, 2014 (3) CD002010. doi: 10.1002/14651858.CD002010.pub4

Probiotics for preventing gestational diabetes (Review)

Barrett, Helen L., Nitert, Marloes Dekker, Conwell, Louise S. and Callaway, Leonie K. (2014). Probiotics for preventing gestational diabetes (Review). Cochrane Database of Systematic Reviews, 2014 (2) CD009951. doi: 10.1002/14651858.CD009951.pub2

Post-transplant lymphoproliferative disorder: no relationship to recombinant human growth hormone use in Australian and New Zealand pediatric kidney transplant recipients

Longmore, Danielle K., Conwell, Louise S., Burke, John R., McDonald, Stephen P. and McTaggart, Steven J. (2013). Post-transplant lymphoproliferative disorder: no relationship to recombinant human growth hormone use in Australian and New Zealand pediatric kidney transplant recipients. Pediatric Transplantation, 17 (8), 731-736. doi: 10.1111/petr.12167

Serum vitamin D levels are lower in Australian children and adolescents with type 1 diabetes than in children without diabetes

Greer, Ristan M., Portelli, Sharon L., Hung, Betsy Shin-Min, Cleghorn, Geoffrey J., McMahon, Sarah K., Batch, Jennifer A. and Conwell, Louise S. (2013). Serum vitamin D levels are lower in Australian children and adolescents with type 1 diabetes than in children without diabetes. Pediatric Diabetes, 14 (1), 31-41. doi: 10.1111/j.1399-5448.2012.00890.x

Probiotics for preventing gestational diabetes (Protocol)

Barrett, Helen L., Nitert, Marloes Dekker, Conwell, Louise S. and Callaway, Leonie K. (2012). Probiotics for preventing gestational diabetes (Protocol). Cochrane Database of Systematic Review (7 ). doi: 10.1002/14651858.CD009951

Bisphosphonates for osteoporosis in people with cystic fibrosis (Review)

Conwell, Louise S. and Chang, Anne B. (2012). Bisphosphonates for osteoporosis in people with cystic fibrosis (Review). Cochrane Database of Systematic Reviews (4). doi: 10.1002/14651858.CD002010.pub3

Hypothalamic obesity following craniopharyngioma surgery: results of a pilot trial of combined metformin and diazoxide therapy

Hamilton, Jill K., Conwell, Louise S., Syme, Catriona, Ahmet, Alexandra, Jefferies, Allison and Daneman, Denis (2011). Hypothalamic obesity following craniopharyngioma surgery: results of a pilot trial of combined metformin and diazoxide therapy. International Journal of Pediatric Endocrinology, 2011 (1). doi: 10.1155/2011/417949

Considering statins for cholesterol-reduction in children if lifestyle and diet changes do not improve their health: A review of the risks and benefits

O’Gorman, Clodagh S.M., O’Neill, Michael B. and Conwell, Louise S. (2011). Considering statins for cholesterol-reduction in children if lifestyle and diet changes do not improve their health: A review of the risks and benefits. Vascular Health and Risk Management, 7 (1), 1-14. doi: 10.2147/VHRM.S7356

Images in pediatric endocrinology: vitamin D deficiency rickets and other nutritional deficiencies in a 12-month-old infant

Brinsmead, Tammy, Frawley, Kieran and Conwell, Louise S. (2011). Images in pediatric endocrinology: vitamin D deficiency rickets and other nutritional deficiencies in a 12-month-old infant. Journal of Pediatric Endocrinology and Metabolism, 24 (1-2), 13-14. doi: 10.1515/JPEM.2011.085

Recognising a metabolic prelude to type 1 diabetes

Conwell, Louise S. (2010). Recognising a metabolic prelude to type 1 diabetes. Journal of Paediatric and Child Health, 46 (4), 207-207. doi: 10.1111/j.1440-1754.2010.01746.x

Klebsiella pneumoniae bacteraemia complicating rotavirus gastroenteritis in two infants with glucocorticoid deficiency

Longmore, DK, Batch, JA, McMahon, SK and Conwell, LS (2010). Klebsiella pneumoniae bacteraemia complicating rotavirus gastroenteritis in two infants with glucocorticoid deficiency. Journal of Pediatric Endocrinology and Metabolism, 23 (3), 293-295. doi: 10.1515/JPEM.2010.23.3.293

The feasibility of a home-based moderate-intensity physical activity intervention in obese children and adolescents

Conwell, Louise S., Trost, Stewart G., Spence, Luke, Brown, Wendy J. and Batch, Jennifer A. (2010). The feasibility of a home-based moderate-intensity physical activity intervention in obese children and adolescents. British Journal of Sports Medicine, 44 (4), 250-255. doi: 10.1136/bjsm.2008.046359

Neonatal complete generalized glucocorticoid resistance and growth hormone deficiency caused by a novel homozygous mutation in helix 12 of the ligand binding domain of the glucocorticoid receptor gene (NR3C1)

McMahon, Sarah K., Pretorius, Carel J., Ungerer, Jacobus P. J., Salmon, Nathaniel J., Conwell, Louise S., Pearen, Michael A. and Batch, Jennifer A. (2010). Neonatal complete generalized glucocorticoid resistance and growth hormone deficiency caused by a novel homozygous mutation in helix 12 of the ligand binding domain of the glucocorticoid receptor gene (NR3C1). Journal of Clinical Endocrinology and Metabolism, 95 (1), 297-302. doi: 10.1210/jc.2009-1003

Use of Continuous Subcutaneous Insulin Infusions (CSII) and Continuous Glucose Monitoring Systems (CGMS) in Cystic-Fibrosis-Related Diabetes (CFRD).

Conwell, Louise S. (2010). Use of Continuous Subcutaneous Insulin Infusions (CSII) and Continuous Glucose Monitoring Systems (CGMS) in Cystic-Fibrosis-Related Diabetes (CFRD).. Infusystems USA and Asia, 5 (3), 17-20.

Differentiated thyroid carcinoma associated with histological features of Hashimoto's thyroiditis

Conwell, L. S., Greer, M. L., Stewart, A. and Perry, C. F. (2009). Differentiated thyroid carcinoma associated with histological features of Hashimoto's thyroiditis. Journal of Pediatric Endocrinology & Metabolism, 22 (11), 991-993. doi: 10.1515/JPEM.2009.22.11.991

Bisphosphonates for osteoporosis in people with cystic fibrosis (Review)

Conwell, Louise S. and Chang, Anne B. (2009). Bisphosphonates for osteoporosis in people with cystic fibrosis (Review). Cochrane Database of Systematic Reviews (4) CD002010. doi: 10.1002/14651858.CD002010.pub2

Novel human pathological mutations. Gene symbol: NR3C1. Disease: glucocorticoid receptor deficiency

Pretorius, C., McMahon, S. K., Ungerer, J. P., Salmon, N., Conwell, L. S. and Batch, J. A. (2009). Novel human pathological mutations. Gene symbol: NR3C1. Disease: glucocorticoid receptor deficiency. Human Genetics, 126 (2), 337-337.

Graves' disease - Acceleration of linear growth

Conwell, L. S. (2009). Graves' disease - Acceleration of linear growth. Journal of Pediatric Endocrinology & Metabolism, 22 (4), 289-290. doi: 10.1515/JPEM.2009.22.4.289

Type 2 Diabetes in Children

Conwell, L. S. (2009). Type 2 Diabetes in Children. Paediatrics and Child Health in General Practice

How to treat - Endocrine disorders of puberty

Conwell, Louise S. and McMahon, Sarah K. (2008). How to treat - Endocrine disorders of puberty. Australian Doctor (9/MAY), 29-36.

Dermatological Complications of Continuous Subcutaneous Insulin Infusion in Children and Adolescents

Conwell, Louise S., Pope, Elena, Artiles, Ana M., Mohanta, Arun, Daneman, Alan and Daneman, Denis (2008). Dermatological Complications of Continuous Subcutaneous Insulin Infusion in Children and Adolescents. The Journal of Pediatrics, 152 (5), 622-628. doi: 10.1016/j.jpeds.2007.10.006

Short stature and metaphyeal dysplasia due to cartilage-hair hypoplasia

Conwell, Louise S., Hermanns, Pia and Zankl, Andreas (2008). Short stature and metaphyeal dysplasia due to cartilage-hair hypoplasia. Journal of Pediatric Endocrinology and Metabolism, 21 (3), 209-211. doi: 10.1515/JPEM.2008.21.3.209

Complications of Insulin Pump Therapy in Children and Adolescents

Conwell, Louise S. and Daneman, Denis (2008). Complications of Insulin Pump Therapy in Children and Adolescents. Infusystems USA and Asia, 5 (4), 25-28.

Necrotizing fasciitis in adolescents with poorly controlled type 1 diabetes mellitus: report of two cases

Conwell, Louise S., Forrest, Christopher R., Allen, Upton D., Perlman, Kusiel and Daneman, Denis (2007). Necrotizing fasciitis in adolescents with poorly controlled type 1 diabetes mellitus: report of two cases. Pediatric diabetes, 8 (6), 397-400. doi: 10.1111/j.1399-5448.2007.00244.x

Oral glucose tolerance test in children and adolescents: Positives and pitfalls

Conwell, L. S. and Batch, J. A. (2004). Oral glucose tolerance test in children and adolescents: Positives and pitfalls. Journal of Paediatrics And Child Health, 40 (11), 620-626. doi: 10.1111/j.1440-1754.2004.00487.x

Aberrant cervical thymus mimicking a cervical mass

Conwell, Louise and Batch, J. A. (2004). Aberrant cervical thymus mimicking a cervical mass. Journal of Paediatrics And Child Health, 40 (9-10), 579-580. doi: 10.1111/j.1440-1754.2004.00468.x

Indexes of insulin resistance and secretion in obese children and adolescents

Conwell, L. S., Trost, S. G., Brown, W. J. and Batch, J. A. (2004). Indexes of insulin resistance and secretion in obese children and adolescents. Diabetes Care, 27 (2), 314-319. doi: 10.2337/diacare.27.2.314

Reversible cardiomyopathy in paediatric Addison's disease a cautionary tale

Conwell, LS, Gray, LM, Delbridge, RG, Thomsett, MJ and Batch, JA (2003). Reversible cardiomyopathy in paediatric Addison's disease a cautionary tale. JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 16 (8), 1191-1195.

Early Adolescent Smoking and a Web of Personal and Social Disadvantage

Conwell, L. S., O'Callaghan, M. J., Andersen, M. J., Najman, J, M., Bor, W. and Williams, G. M. (2003). Early Adolescent Smoking and a Web of Personal and Social Disadvantage. Journal of Paediatrics and Child Health, 39 (8), 580-585. doi: 10.1046/j.1440-1754.2003.00240.x

Reversible Cardiomyopathy in Paediatric Addison’s Disease - A Cautionary Tale

Conwell, L. S., Gray, L. M., Delbridge, R. G., Thomsett, M. J. and Batch, J. A. (2003). Reversible Cardiomyopathy in Paediatric Addison’s Disease - A Cautionary Tale. Journal of Paediatric Endocrinology and Metabolism, 16 (8), 1191-1195.

Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12

Conwell, Louise S., Harraway, James R., Williams, Mark G., Joy, Christopher, Scurry, Bonnie M., Lee, Kevin, McBride, Craig A., Choo, Kelvin, Huynh, Tony, Ng, Carolyn G.L. and Flanagan, Sarah E. (2019). Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12. The European Society of Paediatric Endocrinology Annual Meeting, Vienna, Austria, 19-21 September 2019.

Refractory Hyperinsulinemic Hypoglycemia in Beckwith-Wiedemann Syndrome due to Imprinting Region 1 Gain of Methylation: severity discordant to genotype

Conwell, Louise S., McBride, Craig A., Choo, Kelvin , Tadgell, Shawn C., Fuery, Michelle E. and Davies, Janene R. (2019). Refractory Hyperinsulinemic Hypoglycemia in Beckwith-Wiedemann Syndrome due to Imprinting Region 1 Gain of Methylation: severity discordant to genotype. Updates in Diagnosis and Management of Hyperinsulinism and Neonatal Hypoglycemia Conference, Philadelphia, PA United States, 5-6 September 2019.

Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12

Conwell, Louise S., Harraway, James R., Williams, Mark G., Joy, Christopher, Scurry, Bonnie M., Lee, Kevin, McBride, Craig A., Choo, Kelvin, Huynh, Tony, Ng, Carolyn G.L. and Flanagan, Sarah E. (2019). Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional funding of pancreatic mosaicism for trisomy 12. Updates in Diagnosis and Management of Hyperinsulinism and Neonatal Hypoglycemia Conference, Philadelphia, PA United States, 5-6 September 2019.

Children's Health Queensland Interprofessional Review of Management Decisions in Differences of Sex Development

Conwell, Louise S. (2019). Children's Health Queensland Interprofessional Review of Management Decisions in Differences of Sex Development. Inaugural Children's Health Queensland Interprofessional Practice and Education Symposium, Brisbane, QLD, Australia, 26 June 2019.

Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome

Conwell, Louise and Flanagan, Sarah (2019). Hyperinsulinaemic Hypoglycaemia: A New Presentation of 16p11.2 Duplication Syndrome. 58th Annual Meeting of the European Society for Paediatric Endocrinology (ESPE), Vienna, Austria, September 2019. Basel, Switzerland: Karger.

Hyperinsulinaemic Hypoglycaemia: A new Presentation of 16p11.2 Duplication Syndrome

Conwell, Louise S. and Flanagan, Sarah F. (2019). Hyperinsulinaemic Hypoglycaemia: A new Presentation of 16p11.2 Duplication Syndrome. Updates in Diagnosis and Management of Hyperinsulinism and Neonatal Hypoglycemia Conference, Philadelphia, PA, United States, 5-6 September 2019.

Neonatal Secondary Hyperparathyroidism: a clue to mucolipidosis type II

Papadimos, E.R., Coman, D., Conwell, L.S., McGill, J., Demetriou, K., Inwood, A. and Harris, M. (2019). Neonatal Secondary Hyperparathyroidism: a clue to mucolipidosis type II. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Adelaide, SA, Australia, 27-30 October 2019.

Refractory hyperinsulinaemic hypoglycaemia in Beckwith-Wiedemann syndrome due to imprinting centre 1 gain of methylation: severity discordant to genotype

Conwell, Louise, McBride, Craig, Choo, Kelvin, Tadgell, Shawn, Fuery, Michelle and Davies, Janene (2019). Refractory hyperinsulinaemic hypoglycaemia in Beckwith-Wiedemann syndrome due to imprinting centre 1 gain of methylation: severity discordant to genotype. 58th Annual Meeting of the ESPE, Vienna, Austria, 19-21 September 2019. Basel, Switzerland: S. Karger.

Autonomous thyroid nodule – not just a disease of adulthood

Papadimos, E., Perry, E., Goodwin, B. and Conwell, L. S. (2018). Autonomous thyroid nodule – not just a disease of adulthood. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Newcastle, NSW Australia, July 2018.

Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional finding of pancreatic mosaicism for trisomy 12

Conwell, Louise S., Harroway, James, Williams, Mark, Joy, Christopher, Scurry, Bonnie, Lee, Kevin, McBride, Craig, Choo, Kelvin, Huynh, Tony and Ng, Carolyn G. L. (2018). Congenital hyperinsulinism due to pancreatic mosaicism for paternal uniparental disomy of all chromosome 11, with the additional finding of pancreatic mosaicism for trisomy 12. Australasian Paediatric Endocrine Group Annual Scientific Meetings, Newcastle, Australia, July 2018.

Molecular and functional studies in a case of Familial Congenital Hyperinsulinism: co-inheritance of a dominant and recessive ABCC8 mutation

Conwell, Louise S., Shyng, Show-Ling, Kandasamy, Balamurugan, Wu, Yi and McGown, Ivan (2018). Molecular and functional studies in a case of Familial Congenital Hyperinsulinism: co-inheritance of a dominant and recessive ABCC8 mutation. Australian Functional Genomics Conference, Melbourne, Australia, September 2018.

46,XX Ovotesticular Disorder of Sex Developement (DSD):- duplication of the XX SR region upstream of the critical testicular gene SOX9

Conwell, Louise S., Stathis, Stephen, Franklin, Annie, Borzi, Peter A., Nandini, Adayapalam, Phillips, Gayle E., Ohnesorg, Thomas, Ayers, Katie L. and Sinclair, Andrew H. (2017). 46,XX Ovotesticular Disorder of Sex Developement (DSD):- duplication of the XX SR region upstream of the critical testicular gene SOX9. 3rd Annual Children's Health Queensland Research Symposium, Brisbane, Queensland, Australia, 1 November 2017.

46,XX Ovotesticular Disorder of Sex Development (DSD): duplication of the XX SR region upstream of the critical testicular gene SOX9.

Conwell, Louise S. , Stathis, Stephen , Franklin, Annie , Borzi, Peter A. , Nandini, Adayapalam , Phillips, Gayle E. , Ohnesorg, Thomas , Ayers, Katie L. and Sinclair, Andrew H. (2017). 46,XX Ovotesticular Disorder of Sex Development (DSD): duplication of the XX SR region upstream of the critical testicular gene SOX9.. 10th International Meeting of Pediatric Endocrinology, Washington, United States, 14-17 September 2017.

46,XX Ovotesticular Disorder of Sex Development (DSD):- duplication of the XX SR region upstream of the critical testicular gene SOX9

Conwell, Louise S. , Stathis, Stephen , Franklin, Annie , Borzi, Peter A., Nandini, Adayapalam , Phillips, Gayle E., Ohnesorg, Thomas , Ayers, Katie L. and Sinclair, Andrew H. (2017). 46,XX Ovotesticular Disorder of Sex Development (DSD):- duplication of the XX SR region upstream of the critical testicular gene SOX9. International Disorders of Sexual Development Conference, Copenhagen, Denmark, 29 June-1 July 2017. Copenhagen, Denmark: I-DSD.

Antenatally determined sesquizygosity in gender discordant monochorionic diammniotic twins (46,XX/46XY):- postnatal clinical and gonadal phenotype

Conwell, Louise S., Phillips, Gayle E., Nandini, Adayapalam, Borzi, Peter A. and Gabbett, Michael T. (2017). Antenatally determined sesquizygosity in gender discordant monochorionic diammniotic twins (46,XX/46XY):- postnatal clinical and gonadal phenotype. 3rd Annual Children's Health Queensland Research Symposium, Brisbane, Queensland, Australia, 1 November 2017.

Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46, XX/46, XY): - postnatal clinical and gonadal phenotype

Conwell, Louise S., Phillips, Gayle E., Nandini, Adayapalam, Borzi, Peter A. and Gabbett, Michael T. (2017). Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46, XX/46, XY): - postnatal clinical and gonadal phenotype. 10th International Meeting of Pediatric Endocrinology, Washington, DC, United States, 14 - 17 September 2017. Basel, Switzerland: S. Karger AG. doi: 10.1159/000481424

Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype

Conwell, Louise S. , Phillips, Gayle E., Nandini, Adayapalam , Borzi, Peter A. and Gabbett, Michael T. (2017). Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype. International Disorders of Sexual Development Conference, Copenhagan, Denmark, 29 June-1 July 2017. Copenhagen, Denmark: I-DSD.

Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype

Conwell, Louise S., Phillips, Gayle E. , Nandini, Adayapalam , Borzi, Peter A. and Gabbett, Michael T. (2017). Antenatally determined sesquizygosity in gender discordant monochorionic diamniotic twins (46,XX/46,XY):- postnatal clinical and gonadal phenotype. 10th International Meeting of Pediatric Endocrinology, Washington, DC, United States, 14-17 September 2017.

Co-inheritance of Dominant and Recessive ABCC8 Mutations in a Case of Familial Congenital Hyperinsulinism:- Molecular and Functional Studies

Conwell, Louise S. , Shyng, Show-Ling , Kandasamy, Balamurugan , Wu, Yi , McGown, Ivan , Choo, Kelvin and McBride, Craig (2017). Co-inheritance of Dominant and Recessive ABCC8 Mutations in a Case of Familial Congenital Hyperinsulinism:- Molecular and Functional Studies. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Hobart, Tasmania, Australia, 26-29 November 2017.

Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial Congenital Hyperinsulinism (CHI):- molecular and functional studies

Conwell, Louise S., Shyng, Show-Ling , Kandasamy, Balamurugan , Wu, Yi , McGown, Ivan , Choo, Kelvin and McBride, Craig (2017). Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial Congenital Hyperinsulinism (CHI):- molecular and functional studies. 10th International Meeting of Pediatric Endocrinology, Washington, DC, United States, 14-17 September 2017.

Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism (CHI):- molecular and functional studies

Conwell, Louise S., Shyng, Show-Ling, Kandasamy, Balamurugan, Wu, Yi, Mcgown, Ivan, Choo, Kelvin L. and Mcbride, Craig A. (2017). Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism (CHI):- molecular and functional studies. 10th International Meeting of Pediatric Endocrinology, Washington, DC, United States, 14 - 17 September 2017. Basel, Switzerland: S. Karger AG.

Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism:- molecular and functional studies

Conwell, Louise S., Shyng, Show-Ling, Kandasamy, Balamurugan, Wu, Yi, McGown, Ivan, Choo, Kelvin and McBride, Craig (2017). Co-inheritance of dominant and recessive ABCC8 mutations in a case of familial congenital hyperinsulinism:- molecular and functional studies. 3rd Annual Children's Health Queensland Research Symposium, Brisbane, Queensland, Australia, 1 November 2017.

Early complications of first presentation diabetic ketoacidosis are predicted by severity

Sharwood, Erin F. and Conwell, Louise S. (2017). Early complications of first presentation diabetic ketoacidosis are predicted by severity. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Hobart , Tasmania, Australia, 26-29 November 2017.

Idiopathic Ductopaenia in a Paediatric Patient: A Case Report and Interesting Clinical Biochemistry

Ruddell, Richard G., Burgess, Christopher, Huynh, Tony, Conwell, Louise S., Balouch, Fariha, Burke, Matthew and Pretorius, Carel (2017). Idiopathic Ductopaenia in a Paediatric Patient: A Case Report and Interesting Clinical Biochemistry. Royal College of Pathology Australia Update, Sydney, NSW, Australia, 24 – 26 February 2017.

Idiopathic ductopaenia in a paediatric patient: a case report and interesting clinical biochemistry

Ruddell, Richard G., Burgess, Christopher, Huynh, Tony, Conwell, Louise S., Balouch, Fariha, Burke, Matthew and Pretorius, Carel (2017). Idiopathic ductopaenia in a paediatric patient: a case report and interesting clinical biochemistry. Clinical Lipidology (3rd World Congress), Brisbane, QLD, Australia, unknown.

Lessons Learnt from Two Cases of Congenital Hyperinsulinism from Remote Indigenous Australian Communities

Musthaffa, Yassmin M., Papadimos, Emily R. , Fairchild, Jan , Huynh, Tony and Conwell, Louise S. (2017). Lessons Learnt from Two Cases of Congenital Hyperinsulinism from Remote Indigenous Australian Communities. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Hobart , Tasmania, Australia, 26-29 November 2017.

Turner Syndrome with Ring X Karyotype: Two Cases with Features of the Metabolic Syndrome.

Papadimos, Emily R. and Conwell, Louise S. (2017). Turner Syndrome with Ring X Karyotype: Two Cases with Features of the Metabolic Syndrome.. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Hobart , Tasmania, Australia, 26-29 November 2017.

18[F]-DOPA PET/CT imaging in congenital hyperinsulinism - first 5 years of the Australian experience

Conwell, Louise S., Greer, Ristan M., Fiumara, Frank and Campbell, Louise (2016). 18[F]-DOPA PET/CT imaging in congenital hyperinsulinism - first 5 years of the Australian experience. Congenital Hypoglycaemic Disorders: Hyperinsulinism and Glycogen Storage Disease Conference, Philadelphia, PA, United States, 14-15 April 2016.

Beckwith Wiedemann Syndrome (BWS) in the Context of Mosaic Genome-Wide Paternal Uniparental Disomy (GWpUPD) - Female Infant with Hemihyperplasia, Hyperinsulinism, Benign Tumours and Respiratory Disease

Conwell, Louise S., Williams, Judith A., Davies, Mark, Irving, Helen, Kapur, Nitin and Gattas, Michael (2016). Beckwith Wiedemann Syndrome (BWS) in the Context of Mosaic Genome-Wide Paternal Uniparental Disomy (GWpUPD) - Female Infant with Hemihyperplasia, Hyperinsulinism, Benign Tumours and Respiratory Disease. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Alice Springs, NT Australia, 14 – 17 August 2016.

Beckwith Wiedemann Syndrome (BWS) in the Context of Mosaic Genome-Wide Paternal Uniparental Disomy (GWpUPD) - Female Infant with Hemihyperplasia, Hyperinsulinism, Benign Tumours and Respiratory Disease

Conwell, Louise S., Williams, Judith A., Davies, Mark, Irving, Helen, Kapur, Nitin and Gattas, Michael (2016). Beckwith Wiedemann Syndrome (BWS) in the Context of Mosaic Genome-Wide Paternal Uniparental Disomy (GWpUPD) - Female Infant with Hemihyperplasia, Hyperinsulinism, Benign Tumours and Respiratory Disease. Children's Health Queensland Research Conference, Brisbane, QLD Australia, 2016.

Beckwith Wiedemann Syndrome (BWS) in the Context of Mosaic Genome-Wide Paternal Uniparental Disomy (GwUPD) - Female Infant with Hemihyperplasia, Hyperinsulinism, Benign Tumours and Respiratory Disease

Conwell, Louise S. (2016). Beckwith Wiedemann Syndrome (BWS) in the Context of Mosaic Genome-Wide Paternal Uniparental Disomy (GwUPD) - Female Infant with Hemihyperplasia, Hyperinsulinism, Benign Tumours and Respiratory Disease. Congenital Hypoglycaemic Disorders: Hyperinsulinism and Glycogen Storage Disease Conference, Philadelphia, Pennsylvania USA, 14-15 April 2016.

Insulin Regimens for Newly Diagnosed Children with Type 1 Diabetes in Australia and New Zealand - A Survey of Current Practice

Selvakumar, Dharrshinee , Al-Sallami, Hesham S. , de Bock, Martin , Ambler, Geoffrey R. , Aguirre, Paul B. , Wiltshire, Esko , Tham, Elaine , Simm, Peter , Conwell, Louise S. , Carter, Phillipa , Willis, Jinny , Wheeler, Benjamin J. and PSNZ Diabetes Clinical Network (2016). Insulin Regimens for Newly Diagnosed Children with Type 1 Diabetes in Australia and New Zealand - A Survey of Current Practice. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Alice Springs, Northern Territory, Australia, 14 – 17 August 2016.

Massively parallel sequencing to determine the prevalence of maturity onset diabetes of the young in an entire paediatric diabetes clinic including antibody positive type 1 diabetes

Johnson, Stephanie R., Davis, Elizabeth, Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2016). Massively parallel sequencing to determine the prevalence of maturity onset diabetes of the young in an entire paediatric diabetes clinic including antibody positive type 1 diabetes. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Alice Springs, NT, Australia, unknown.

1,5-Anhydroglucitol, the most discriminatory metabolomic marker measured by Gas Chromatography-Mass Spectrometry in adolescents with Type 1 Diabetes compared to control subjects - High correlation with Glycomark assay

Conwell, Louise S., Hodson, Mark P., Chrysanthopoulos, Panagiotis K., Greer, Ristan M., Nielsen, Lars K., Cardinal, John W., Sanders, L., Gous, R. and Baskerville, Tracey (2015). 1,5-Anhydroglucitol, the most discriminatory metabolomic marker measured by Gas Chromatography-Mass Spectrometry in adolescents with Type 1 Diabetes compared to control subjects - High correlation with Glycomark assay. Children's Health Queensland Research Conference, unknown, unknown.

1,5-Anhydroglucitol, the most discriminatory metabolomic marker measured by Gas Chromatography-Mass Spectrometry in adolescents with Type 1 Diabetes compared to control subjects - high correlation with Glycomark assay

Conwell, Louise S., Hodson, Mark P., Chrysanthopoulos, Panagiotis K., Greer, Ristan M., Nielsen, Lars K., Cardinal, John W., Sanders, L., Gous, R. and Baskerville, Tracey (2015). 1,5-Anhydroglucitol, the most discriminatory metabolomic marker measured by Gas Chromatography-Mass Spectrometry in adolescents with Type 1 Diabetes compared to control subjects - high correlation with Glycomark assay. International Society of Paediatric and Adolescent Diabetes / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Brisbane, QLD, Australia, October 2015.

18[F]-DOPA PET/CT imaging in Congenital Hyperinsulinism - first 5 years of the Australian experience

Conwell, Louise S., Greer, Ristan M., Fiumara, Frank and Campbell, Louise (2015). 18[F]-DOPA PET/CT imaging in Congenital Hyperinsulinism - first 5 years of the Australian experience. Children's Health Queensland Research Conference, Brisbane, Queensland, Australia, December 2015.

18[F]-DOPA PET/CT imaging in congenital hyperinsulinism - first 5 years of the Australian experience

Conwell, Louise S., Greer, Ristan M., Fiumara, Frank and Campbell, Louise (2015). 18[F]-DOPA PET/CT imaging in congenital hyperinsulinism - first 5 years of the Australian experience. International Society of Paediatric and Adolescent Diabetes / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Brisbane, QLD, Australia, October 2015.

A tale of two syndromes: an instructive case of two synchronous variants in ABCC8 and DICER1

Conwell, L. S., Wu, M. K., deBock, L., King, B. R., Stewart, C. J., Choong, C. S. and Foulkes, W. D. (2015). A tale of two syndromes: an instructive case of two synchronous variants in ABCC8 and DICER1. International Society of Paediatric and Adolescent Diabetes / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Brisbane, Queensland, Australia, October 2015.

A tale of two syndromes: an instructive case of two synchronous variants in ABCC8 and DICER1

Conwell, L. S., Wu, M. K., deKock, L., King, B. R., Stewart, C. J., Choong, C. S. and Foulkes, W. D. (2015). A tale of two syndromes: an instructive case of two synchronous variants in ABCC8 and DICER1. Children's Health Queensland Research Conference, Brisbane, Queensland, Australia, December 2015.

Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy

Sharwood, Erin F., McGill, Michael, Koorts, P. J., Coman, David and Conwell, Louise S. (2015). Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy. International Society of Paediatric and Adolescent Diabetes / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Brisbane, Queensland, Australia, October 2015.

Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy

Sharwood, E. F., McGill, M., Koorts, P. J., Coman, D. and Conwell, L. S. (2015). Dizygotic twins with skeletal dysplasia and resistance to hormones signalling through G protein-coupled receptors and the Gsa/cAMP/PKA pathway - severe craniosynostosis and hypertrophic cardiomyopathy. Children's Health Queensland Research Conference, Brisbane, Queensland, Australia, December 2015.

Prevalence of Maturity Onset Diabetes of the Young in a Western Australia paediatric diabetes clinic using targeted Massively Parallel Sequencing

Johnson, Stephanie R., Davis, Elizabeth, Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2015). Prevalence of Maturity Onset Diabetes of the Young in a Western Australia paediatric diabetes clinic using targeted Massively Parallel Sequencing. Children's Health Queensland Research Conference, Brisbane Qld Australia, December 2015.

Prevalence of Maturity Onset Diabetes of the young in a Western Australian paediatric diabetes clinic using targeted Massively Parallel Sequencing

Johnson, Stephanie R., Davis, Elizabeth, Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2015). Prevalence of Maturity Onset Diabetes of the young in a Western Australian paediatric diabetes clinic using targeted Massively Parallel Sequencing. International Society of Paediatric and Adolescent Diabetes / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Brisbane, Queensland, Australia: University of Queensland, October 2015.

1,5-Anhydroglucitol, an indicator of short term glycaemic control, is the most discriminatory metabolomic marker in adolescents with type 1 diabetes compared to control subjects

Conwell, Louise S., Hodson, Mark P., Chrysanthopoulos, Panagiotis K., Greer, Ristan M. and Baskerville, Tracey (2014). 1,5-Anhydroglucitol, an indicator of short term glycaemic control, is the most discriminatory metabolomic marker in adolescents with type 1 diabetes compared to control subjects. APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting, Darwin, NT, Australia, 29 October-1 November, 2014.

Altered cardiac structure, diastolic function and markers of cardiovascular risk (inflammation, oxidative stress and endothelial dysfunction) in adolescents with type 1 diabetes

Conwell, Louise S., Baskerville, Tracey, Duncan, Danusia, Greer, Ristan M., Coombes, Jeff S., Cardinal, John, Leong, Gary M., Harris, Mark and Kostner, Karam (2014). Altered cardiac structure, diastolic function and markers of cardiovascular risk (inflammation, oxidative stress and endothelial dysfunction) in adolescents with type 1 diabetes. APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting, Darwin, NT, Australia, 29 October-1 November, 2014.

Next generation sequencing for maturity onset diabetes of the young

Johnson, Stephanie R., Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2014). Next generation sequencing for maturity onset diabetes of the young. ISPAD 2014: 40th Annual Meeting of the International Society of Pediatric and Adolescent Diabetes, Toronto, ON, Canada, 3-6 September, 2014. Berlin, Germany: K.I.T. Group.

Next generation sequencing for maturity onset diabetes of the young

Johnson, Stephanie R., Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2014). Next generation sequencing for maturity onset diabetes of the young. APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting, Darwin, NT, Australia, 29 October-1 November, 2014.

Next generation sequencing to identify a novel INS gene mutation in a family with Maturity Onset Diabetes of the Young (MODY)

Johnson, Stephanie R., McGown, Ivan N., Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2014). Next generation sequencing to identify a novel INS gene mutation in a family with Maturity Onset Diabetes of the Young (MODY). APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting, Darwin, NT, Australia, 29 October-1 November, 2014.

Novel heterozygous deletion in the HNF1B-MODY5 gene - Adolescent with antibody negative diabetes, longstanding hyperglycaemia without ketosis, cataracts, small echogenic kidneys with cortical cyst, pancreatic atrophy, exocrine pancreatic insufficiency and

Conwell, Louise S. and McGown, Ivan P. (2014). Novel heterozygous deletion in the HNF1B-MODY5 gene - Adolescent with antibody negative diabetes, longstanding hyperglycaemia without ketosis, cataracts, small echogenic kidneys with cortical cyst, pancreatic atrophy, exocrine pancreatic insufficiency and. APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting, Darwin, NT, Australia, 29 October-1 November, 2014.

Resistance training improves metainflammation and body composition in obese adolescents

Dayiha, Rachana, Schultz, Sarah P., Cardinal, John, Byrne, Nuala, Hills, Andrew P., Gibbons, Kristen, Conwell, Louise S., Harris, Mark and Leong, Gary M. (2014). Resistance training improves metainflammation and body composition in obese adolescents. APPES & APEG 2014: Asia Pacific Paediatric Endocrine Society & Australasian Paediatric Endocrine Group Joint Annual Scientific Meeting, Darwin, NT, Australia, 29 October-1 November, 2014.

Resistance training improves metainflammation and body composition in obese adolescents

Dayiha, Rachana, Schultz, Sarah P., Cardinal, John, Byrne, Nuala, Hills, Andrew P., Gibbons, Kristen, Conwell, Louise S., Harris, Mark and Leong, Gary M. (2014). Resistance training improves metainflammation and body composition in obese adolescents. ENDO 2014: Endocrine Society 96th Annual Scientific Meeting & Expo, Chicago, IL, USA, 21-24 June, 2014. Chevy Chase, MD, United States: The Endocrine Society. doi: 10.1210/endo-meetings.2014.OABA.17.SUN-0921

Altered cardiac structure, diastolic function and markers of cardiovascular risk (inflammation, oxidative stress and endothelial dysfunction) in adolescents with type 1 diabetes

Conwell, Louise S., Baskerville, Tracey, Duncan, Danusia, Greer, Ristan M., Coombes, Jeff S., Leong, Gary M., Harris, Mark and Kostner, Karam (2013). Altered cardiac structure, diastolic function and markers of cardiovascular risk (inflammation, oxidative stress and endothelial dysfunction) in adolescents with type 1 diabetes. APEG 2013: Australasian Paediatric Endocrine Group Annual Scientific Meeting, Sydney, NSW, Australia, 28-31 July, 2013.

Altered cardiovascular risk markers, cardiac structure and cardiac function in adolescents with type 1 diabetes

Conwell, Louise S., Baskerville, Tracey, Duncan, Danusia, Greer, Ristan M., Coombes, Jeff S., Cardinal, John, Leong, Gary M., Harris, Mark and Kostner, Karam (2013). Altered cardiovascular risk markers, cardiac structure and cardiac function in adolescents with type 1 diabetes. WDC 2013: 22nd World Diabetes Congress & IDF 2013: International Diabetes Federation Scientific Meeting, Melbourne, VIC, Australia, 2-6 December, 2013. Brussels, Belgium: International Diabetes Federation.

Impaired left ventricular diastolic function in overweight youth is associated with insulin resistance, subclinical inflammation and adipokine dysregulation: a novel cardiometabolic link

Dayiha, Rachana, Schultz, Sarah P., Gibbons, Kristen, Duncan, Danusia, Cardinal, John, Kostner, Karam, Byrne, Nuala, Hills, Andrew P., Harris, Mark, Conwell, Louise S. and Leong, Gary Martin (2013). Impaired left ventricular diastolic function in overweight youth is associated with insulin resistance, subclinical inflammation and adipokine dysregulation: a novel cardiometabolic link. ENDO 2013: Endocrine Society 95th Annual Scientific Meeting & Expo, San Francisco, CA, USA, 15-18 June, 2013. Chevy Chase, MD, United States: The Endocrine Society. doi: 10.1210/endo-meetings.2013.OABA.12.SAT-693

Next-generation sequencing (NGS) to identify a novel INS gene mutation in a family with maturity onset diabetes of the young (MODY)

Johnson, Stephanie R., McGown, Ivan N., Conwell, Louise S., Harris, Mark and Duncan, Emma L. (2013). Next-generation sequencing (NGS) to identify a novel INS gene mutation in a family with maturity onset diabetes of the young (MODY). LWPES/ESPE 9th Joint Meeting Global Care in Pediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, Milan, Italy, 19-22 September, 2013. Basel, Switzerland: S. Karger. doi: 10.1159/isbn.978-3-318-02505-7

10 year trend for diabetic ketoacidosis in children at diagnosis of type 1 diabetes from Brisbane

Willis, Carol M., Cotterill, Andrew M., Conwell, Louise S., McMahon, Sarah K., Harris, Mark, Leong, Gary M., Kearney, Helen, Shann, Karen, Noud, Marina, Cardinal Sherell and Batch, Jennifer A. (2012). 10 year trend for diabetic ketoacidosis in children at diagnosis of type 1 diabetes from Brisbane. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Queenstown, New Zealand, 29 July - 2 August 2012.

10 year trend for diabetic ketoacidosis in children at diagnosis of type 1 diabetes from Brisbane

Willis, Carol M., Cotterill, Andrew M., Conwell, Louise S., McMahon, Sarah K., Harris, Mark, Leong, Gary M., Yates, Jason M., Kearney, Helen, Shann, Karen, Noud, Marina, Cardinal, Sherell and Batch, Jennifer A. (2012). 10 year trend for diabetic ketoacidosis in children at diagnosis of type 1 diabetes from Brisbane. ISPAD 2012: 38th Annual Meeting of the International Society of Pediatric and Adolescent Diabetes, Istanbul, Turkey, 10-13 October, 2012.

A case of hyperinsulinism-hyperammonaemia syndrome

Buchanan, Kerry, Williams, Judith A., Greer, Ristan M., Fiumara, Frank, Campbell, Louise, Cowley, David, McGown, Ivan M., Batch, Jennifer A., McMahon, Sarah K. and Conwell, Louise S. (2012). A case of hyperinsulinism-hyperammonaemia syndrome. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Queenstown, New Zealand, July 29 - August 2 2012.

Carbimazole associated arthralgia: more common than we think?

Scott, Amanda J., Conwell, Louise S., McMahon, Sarah K. and Batch, Jennifer A. (2012). Carbimazole associated arthralgia: more common than we think?. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Queenstown, New Zealand, July 29 - August 2 2012.

Predicting the length of honeymoon in newly diagnosed children with type 1 diabetes mellitus based on age, initial HbA1c and acid base status

Yates, Jason, Conwell, Louise, Johnson, Stephanie, McMahon, Sarah, Hughes, Ian, Harris, Mark, Batch, Jennifer and Cotterill, Andrew (2012). Predicting the length of honeymoon in newly diagnosed children with type 1 diabetes mellitus based on age, initial HbA1c and acid base status. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Queenstown, New Zealand, 29 July - 2 August 2012.

[18F]-DOPA PET/CT Imaging in Congenital Hyperinsulinism - First 12 months of the Australian experience.

Conwell, L. S., Greer, R. M., Walker, R. M., Fiumara, F., Campbell, L., Harris, M. and Cotterill, A. M. (2012). [18F]-DOPA PET/CT Imaging in Congenital Hyperinsulinism - First 12 months of the Australian experience.. Monogenic Disorders of Insulin Secretion: Congenital Hyperinsulinism and Neonatal Disorders, Philadelphia Pennsylvania, 15-16 March 2012. Malden, MA, United States: Wiley-Blackwell Publishing. doi: 10.1111/j.1399-5448.2012.00887.x

[18F]-DOPA PET/CT imaging in congenital hyperinsulinism - first 2 years of the Queensland experience

Conwell, Louise S., Greer, R. M., Walker, Ristan M., Fiumara, Frank, Campbell, Louise, Cowley, David, McGowan, Ivan M, Harris, Mark, Leong, Gary M., Batch, Jennifer A., McMahon, Sarah K., Dahiya, Rachana and Cotterill, Andrew M. (2012). [18F]-DOPA PET/CT imaging in congenital hyperinsulinism - first 2 years of the Queensland experience. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Queenstown, New Zealand, 28 July - 2 August 2012.

Adolescents with type 1 diabetes mellitus have normal diastolic function in the context of normal carotid intima-media thickness and normal plasma lipid levels

Conwell, Louise S., Baskerville, Tracey, Leong, Gary M., Harris, Mark and Kostner, Karam (2011). Adolescents with type 1 diabetes mellitus have normal diastolic function in the context of normal carotid intima-media thickness and normal plasma lipid levels. Endocrine Society of Australia Annual Scientific Meeting / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Perth, Australia, 31 August - 2 September 2011.

Adolescents with type 1 diabetes mellitus have normal diastolic function in the context of normal carotid intima-media thickness and normal plasma lipid levels.

Louise S. Conwell, Tracey Baskerville, Gary M Leong, Mark Harris and Karam Kostner (2011). Adolescents with type 1 diabetes mellitus have normal diastolic function in the context of normal carotid intima-media thickness and normal plasma lipid levels.. Endocrine Society of Australia Annual Scientific Meeting / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Perth, Australia, August 31 to September 2 2011.

Asymptomatic ST elevation on ECG in a 13 year old patient with Grave's thyrotoxicosis: A case report

Scott AJ, Colen T, Morwood J and Conwell LS (2011). Asymptomatic ST elevation on ECG in a 13 year old patient with Grave's thyrotoxicosis: A case report. Endocrine Society of Australia / Australasian Paediatric Endocrine Group Annual Scientific Meeting, Perth WA, Australia, August 31 to September 2 2011.

Management and health outcomes in young people with diabetes: a 10 year review.

Lang E, Cotterill A and Conwell LS (2011). Management and health outcomes in young people with diabetes: a 10 year review.. Australian Diabetes Endocrine Group State Conference, Brisbane Australia, June 2011.

Growth hormone deficiency and adrenal insufficiency in a case of primordial dwarfism.

Buchanan K, Batch JA, Conwell LS and McMahon SK (2010). Growth hormone deficiency and adrenal insufficiency in a case of primordial dwarfism.. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Adelaide Australia, August 2010.

Insulin Aspart-Induced Lipoatrophy in a 12 year old patient with type 1 diabetes mellitus: a case report.

Scott AJ, Batch JA, Conwell LS and McMahon SK (2010). Insulin Aspart-Induced Lipoatrophy in a 12 year old patient with type 1 diabetes mellitus: a case report.. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Adelaide Australia, August 2010.

Post-transplant lymphoproliferative disorder in Australian and New Zealand pediatric renal transplant recipients

McTaggart, Steven, Longmore, Danielle, Conwell, Louise S., McDonald, Stephen P. and Burke, John R. (2010). Post-transplant lymphoproliferative disorder in Australian and New Zealand pediatric renal transplant recipients. XXII International Congress of the Transplantation Society, Vancouver BC, Canada, August 2010. Philadelphia, PA, United States: Lippincott Williams & Wilkins.

Recombinant human growth hormone is not associated with post-transplant lymphoproliferative disorder in Australian and New Zealand Paediatric Renal Transplant Recipients.

Longmore D, Conwell LS, McDonald SP, Burke JR and Hughes IP (2010). Recombinant human growth hormone is not associated with post-transplant lymphoproliferative disorder in Australian and New Zealand Paediatric Renal Transplant Recipients.. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Adelaide, Australia, August 2010.

'Sweet program': effective transition of young people with diabetes to adult care in Queensland, Australia

Lang, E. G., Bowden, T., Conwell, L. S., Kamp, M. and Cotterill, A. (2009). 'Sweet program': effective transition of young people with diabetes to adult care in Queensland, Australia. LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, New York, N.Y., USA, 9-12 September 2009. BASEL: KARGER. doi: 10.1159/000239668

A 10 year review of clinical outcomes and complication screening practices in young people with diabetes

Lang, E. G., Conwell, L. S., Kamp, M. and Cotterill, A. (2009). A 10 year review of clinical outcomes and complication screening practices in young people with diabetes. LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, New York, N.Y., USA, 9-12 September 2009. BASEL: KARGER. doi: 10.1159/000239668

Hypothalamic obesity following craniopharyngioma surgery: Results of a pilot trial of combined diazoxide and metformin therapy

Hamilton, J., Conwell, L. S., Ahmet, A., Jeffery, A. and Daneman, D. (2009). Hypothalamic obesity following craniopharyngioma surgery: Results of a pilot trial of combined diazoxide and metformin therapy. 35th Annual Meeting of the International Society of Pediatric and Adolescent Diabetes (ISPAD), Ljubljana, Slovenia, 2-5 September 2009. Malden, MA, United States: Wiley-Blackwell Publishing. doi: 10.1111/j.1399-5448.2009.00554.x

Klebsiella pneumoniae sepsis complicating rotavirus gastroenteritis in two infants with glucocorticoid deficiency

Longmore, Danielle K., Batch, Jennifer A., McMahon, Sarah K. and Conwell, Lousie S. (2009). Klebsiella pneumoniae sepsis complicating rotavirus gastroenteritis in two infants with glucocorticoid deficiency. LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology, New York City, N.Y. USA, 9-12 September 2009. Switzerland: S. Karger AG.

Lipid levels in adolescents with type 1 diabetes are frequently outside current recommendations

Burgess, C. and Conwell, L. (2009). Lipid levels in adolescents with type 1 diabetes are frequently outside current recommendations. Royal Australasian College of Physicians Annual Scientific Conference, Sydney , Australia, May 2009.

Lipid levels in children and adolescents with type 1 diabetes are frequently outside current recommendations

Burgess, C., Willis, C. and Conwell, L. S. (2009). Lipid levels in children and adolescents with type 1 diabetes are frequently outside current recommendations. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Coolum, QLD, Australia, November 2009.

Lipid levels in children and adolescents with type 1 diabetes are frequently outside current recommendations

Conwell, Louise S. and Burgess, Christopher J. (2009). Lipid levels in children and adolescents with type 1 diabetes are frequently outside current recommendations. LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology, New York City, N.Y. USA, 9-12 September 2009. Switzerland: S. Karger AG.

Multiple endocrine neoplasia type 1 in childhood: how screening guidelines correlate with real life experience

Gallego, PH, Harris, M, Leong, G, Russel, A, Cardinal, J, Conwell, LS and Cotterill, A (2009). Multiple endocrine neoplasia type 1 in childhood: how screening guidelines correlate with real life experience. LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, New York, N.Y., USA, 9-12 September 2009. BASEL: KARGER. doi: 10.1159/000239668

Obesity accentuates the age-associated increase in arterial stiffness during adolescence

Conwell, LS, Sharman, JE, Coombes, JS and Batch, JA (2009). Obesity accentuates the age-associated increase in arterial stiffness during adolescence. LWPES/ESPE 8th Joint Meeting Global Care in Pediatric Endocrinology in collaboration with APEG, APPES, JSPE and SLEP, New York, NY, 9-12 September, 2009. BASEL: KARGER. doi: 10.1159/000239668

Sweet Program:- Effective transition of young people with diabetes to adult care in Queensland.

Bowden T, Lang E, Conwell LS, Kamp M and Cotterill A (2009). Sweet Program:- Effective transition of young people with diabetes to adult care in Queensland.. Australian Diabetes Educators Association, Adelaide Australia, 2009.

Children with type 1 diabetes have low serum vitamin D compared with controls

Greer, R. M., Debonis, S., Hung, S. H., Batch, J. A., Cleghorn, G. J., Conwell, L. and McMahon, S. (2008). Children with type 1 diabetes have low serum vitamin D compared with controls. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Canberra, Australia, 17-19 November, 2008.

Combined diazoxide and metformin therapy for hypothalamic obesity secondary to craniopharyngioma in children:- effectiveness predicted by area-under-curve for insulin in Oral Glucose Tolerance Test (OGTT).

Conwell, L.S., Odrobina, A., Ahmet, A., Daneman, D. and Hamilton, J. (2008). Combined diazoxide and metformin therapy for hypothalamic obesity secondary to craniopharyngioma in children:- effectiveness predicted by area-under-curve for insulin in Oral Glucose Tolerance Test (OGTT).. Australian and New Zealand Obesity Society Annual Scientific Meeting, Brisbane Australia, November 2008.

Diabetes in motion in the year of the child. Meeting highlights

Conwell, Louise S. and Codner, Ethel (2008). Diabetes in motion in the year of the child. Meeting highlights. 33rd Annual ISPAD Meeting and 5th Symposium on Diabetic Angiopathy in Children, Berlin, Germany, 26-29 September and 30 September, 2007. Copenhagen, DK: Munksgaard. doi: 10.1111/j.1399-5448.2007.00346.x

Diazoxide and metformin therapy in children with hypothalamic obesity secondary to craniopharyngioma: A pilot study

Conwell, L. S., Odrobina, E., Ahmet, A., Daneman, D. and Hamilton, J. (2008). Diazoxide and metformin therapy in children with hypothalamic obesity secondary to craniopharyngioma: A pilot study. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Canberra Australia, November 2008.

Klebsielle pneumoniae sepsis complicating rotavirus gastroenteritis in two infants with glucocorticoid deficiency.

Longmore DK, Batch JA and Conwell LS (2008). Klebsielle pneumoniae sepsis complicating rotavirus gastroenteritis in two infants with glucocorticoid deficiency.. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Canberra Australia, November 2008.

Polysyndactyly renal hypoplasia and central precocious puberty:- a case of Pallister-Hall syndrome

Jensen, Diane E., McCreanor, John, McTaggart, Steven, Gabbett, Michael and Conwell, Louise S. (2008). Polysyndactyly renal hypoplasia and central precocious puberty:- a case of Pallister-Hall syndrome. Asia Pacific Endocrine Society Annual Scientific Meeting, Korea, October 2008.

Polysyndactyly, Renal Hypoplasia and Central Precocious Puberty: A Case of Pallister-Hall Syndrome

Jensen, Diane, McCreanor, John, McTaggart, Stephen, Gabbett, Michael and Conwell, Louise (2008). Polysyndactyly, Renal Hypoplasia and Central Precocious Puberty: A Case of Pallister-Hall Syndrome. BASEL: KARGER.

Reduced serum vitamin D levels are associated with type 1 diabetes in Queensland children: a case control study

Greer, R. M., Debonis, S., Hung, B., Batch, J. A., Conwell, L., McMahon, S. and Cleghorn, G. J. (2008). Reduced serum vitamin D levels are associated with type 1 diabetes in Queensland children: a case control study. Combined Conference of the Australasian Faculty of Occupational & Environmental Medicine (AFOEM) and the Australasian Faculty of Rehabilitation Medicine (AFRM), Adelaide, SA Australia, 7 - 9 May 2008.

A novel ROMK mutation in a child presenting with bartter syndrome type 2

Mallik, M., Conwell, L., Bichet, D., Sochett, E. and Hebert, D. (2007). A novel ROMK mutation in a child presenting with bartter syndrome type 2. NEW YORK: SPRINGER.

Dermatological complications of continuous subcutaneous insulin infusion (CSII) in children and adolescents: An observational study

Conwell, Louise S., Artiles, Ana, Pope, Elena, Mohanta, Arun, Daneman, Alan and Daneman, Denis (2007). Dermatological complications of continuous subcutaneous insulin infusion (CSII) in children and adolescents: An observational study. 67th Annual Meeting of the American-Diabetes-Association, Chicago Il, Jun 22-26, 2007. ALEXANDRIA: AMER DIABETES ASSOC.

A novel ROMK mutation in a child presenting with Bartter Syndrome Type 2

Malik, M., Conwell, L.S., Bichet, D.G., Sochett, E. and Hebert, D. (2007). A novel ROMK mutation in a child presenting with Bartter Syndrome Type 2. International Pediatric Nephrology Association Annual Scientific Meeting, Budapest, Hungary, 2007.

Alanine transaminase in adolescence is predicted by adiposity, free fatty acids and tumour necrosis factor-alpha

Conwell, L. S., Coombes, J. S. and Batch, J. A. (2007). Alanine transaminase in adolescence is predicted by adiposity, free fatty acids and tumour necrosis factor-alpha. 67th Annual Meeting of the American Diabetes Association, Chicago, IL, United States, 22-26 June 2007. ALEXANDRIA: American Diabetes Association.

Dermatological Complications of Insulin Pump Use in the Paediatric Population

Conwell, L. S., Pope, E., Artiles, A. M., Mohanta, A., Daneman, A. and Daneman, D. (2007). Dermatological Complications of Insulin Pump Use in the Paediatric Population. International Society of Pediatric and Adolescent Diabetes, Berlin, Germany, September 2007.

Polysyndactyly, renal hypoplasia and central precocious puberty:- a case of Pallister-Hall Syndrome.

Jensen DE, McCreanor J, McTaggart S, Gabbett M and Conwell LS (2007). Polysyndactyly, renal hypoplasia and central precocious puberty:- a case of Pallister-Hall Syndrome.. Australasian Paediatric Endocrine Group Annual Scientific Meeting, Broome Australia, October 2007.

Dermatological Complications of Continuous Subcutaneous Insulin Infusion (CSII) in Children and Adolescents

Conwell LS, Pope E, Artiles AM, Mohanta A, Daneman A and Daneman D (2006). Dermatological Complications of Continuous Subcutaneous Insulin Infusion (CSII) in Children and Adolescents. Canadian Society for Endocrinology and Metabolism Annual Scientific Meeting, Toronto, Canada, October 2006.

Necrotizing Fasciitis in Adolescents with Poorly Controlled Type 1 Diabetes - Report of 2 cases

Conwell LS, Perlman K and Daneman D (2006). Necrotizing Fasciitis in Adolescents with Poorly Controlled Type 1 Diabetes - Report of 2 cases. American Diabetes Association Annual Scientific Meeting, Washinton, DC, U.S.A., June 2006.

Necrotizing fasciitis in two adolescents with poorly controlled type 1 diabetes

Conwell LS, Forrest CR, Allen UD, Perlman K and Daneman D (2006). Necrotizing fasciitis in two adolescents with poorly controlled type 1 diabetes. Canadian Paediatric Endocrine Group Annual Scientific Meeting, Edmonton, Canada, February 2006. ALEXANDRIA: AMER DIABETES ASSOC.

The effect of guided care on quality of care.

Boyd, CM, Shadmi, E, Conwell, L, Sylvia, M, Boult, C, Brager, R, Leff, B and Scharfstein, D (2005). The effect of guided care on quality of care.. Annual Meeting of the American-Geriatrics-Society, Orlando Fl, May 11-15, 2005. HOBOKEN: WILEY-BLACKWELL.

Cardiovascular Risk Factors and Insulin Resistance in Obese Adolescents

Conwell LS, Coombes JS, Sharman JE and Batch JA (2005). Cardiovascular Risk Factors and Insulin Resistance in Obese Adolescents. ESPE / Lawson Wilkin's International Paediatric Endocrinology Scientific Meeting, Lyon, France, September 2005.

Evaluation of a pedometer-based, moderate-intensity physical activity program for obese children and adolescents

Trost, S. G., Conwell, L. S., Spence, L., Brown, W. J. and Batch, J. A. (2003). Evaluation of a pedometer-based, moderate-intensity physical activity program for obese children and adolescents. American College of Sports Medicine 50th Annual Meeting, San Francisco, CA, U.S.A, 28-31 May, 2003. Philadelphia, PA, U.S.A.: Lippincott, Williams & Wilkins.

Insulin resistance and cardiovascular risk factors in obese children and adolescents

Conwell, Louise Sonia (2006). Insulin resistance and cardiovascular risk factors in obese children and adolescents. PhD Thesis, School of Medicine, The University of Queensland. doi: 10.14264/uql.2017.19