The University of Queensland

The impact of donor/recipient age difference and HLA mismatch on graft outcome in pediatric kidney transplantation

Trnka, Peter, McTaggart, Steven J. and Francis, Anna (2018) The impact of donor/recipient age difference and HLA mismatch on graft outcome in pediatric kidney transplantation. Pediatric Transplantation, e13265. doi:10.1111/petr.13265

Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms

Forbes, Thomas A., Howden, Sara E., Lawlor, Kynan, Phipson, Belinda, Maksimovic, Jovana, Hale, Lorna, Wilson, Sean, Quinlan, Catherine, Ho, Gladys, Holman, Katherine, Bennetts, Bruce, Crawford, Joanna, Trnka, Peter, Oshlack, Alicia, Patel, Chirag, Mallett, Andrew, Simons, Cas and Little, Melissa H. (2018) Patient-iPSC-derived kidney organoids show functional validation of a ciliopathic renal phenotype and reveal underlying pathogenetic mechanisms. American Journal of Human Genetics, 102 5: 816-831. doi:10.1016/j.ajhg.2018.03.014

Therapeutic plasma exchange normalizes insulin-mediated response in a child with type 1 diabetes and insulin autoimmune syndrome

Sharwood, Erin F., Hughes, Ian P., Pretorius, Carel J., Trnka, Peter, Peake, Jane and Huynh, Tony (2017) Therapeutic plasma exchange normalizes insulin-mediated response in a child with type 1 diabetes and insulin autoimmune syndrome. Pediatric Diabetes, 48 1: S89-179. doi:10.1111/pedi.12522

Long-term outcome of kidney transplantation in recipients with focal segmental glomerulosclerosis

Francis, Anna, Trnka, Peter and McTaggart, Steven J. (2016) Long-term outcome of kidney transplantation in recipients with focal segmental glomerulosclerosis. Clinical Journal of the American Society of Nephrology, 11 11: 2041-2046. doi:10.2215/CJN.03060316

A protocol for the identification and validation of novel genetic causes of kidney disease

Mallett, Andrew, Patel, Chirag, Maier, Barbara, McGaughran, Julie, Gabbett, Michael, Takasato, Minoru, Cameron, Anne, Trnka, Peter, Alexander, Stephen I., Rangan, Gopala, Tchan, Michel C., Caruana, Georgina, John, George, Quinlan, Cathy, McCarthy, Hugh J., Hyland, Valentine, Hoy, Wedy E., Wolvetang, Ernst, Taft, Ryan, Simons, Cas, Healy H. and Little, Melissa (2015) A protocol for the identification and validation of novel genetic causes of kidney disease. BMC Nephrology, 16 152: . doi:10.1186/s12882-015-0148-8

A retrospective review of telehealth services for children referred to a paediatric nephrologist

Trnka, Peter, White, Megan M., Renton, William D., McTaggart, Steven J., Burke, John R. and Smith, Anthony C. (2015) A retrospective review of telehealth services for children referred to a paediatric nephrologist. BMC Nephrology, 16 125: 1-7. doi:10.1186/s12882-015-0127-0

KHA-CARI guideline: diagnosis and treatment of urinary tract infection in children

McTaggart, Steven, Danchin, Margie, Ditchfield, Michael, Hewitt, Ian, Kausman, Joshua, Kennedy, Sean, Trnka, Peter and Williams, Gabrielle (2015) KHA-CARI guideline: diagnosis and treatment of urinary tract infection in children. Nephrology, 20 2: 55-60. doi:10.1111/nep.12349

Reninoma: an uncommon cause of renin-mediated hypertension

Trnka, Peter, Orellana, Luisa, Walsh, Mark, Pool, Louis and Borzi, Peter (2014) Reninoma: an uncommon cause of renin-mediated hypertension. Frontiers in Pediatrics, 2 89: 1-7. doi:10.3389/fped.2014.00089

Henoch-Schonlein purpura in children

Trnka, Peter (2013) Henoch-Schonlein purpura in children. Journal of Paediatrics and Child Health, 49 12: 995-1003. doi:10.1111/jpc.12403

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans

Halbritter, Jan, Bizet, Albane A., Schmidts, Miriam, Porath, Jonathan D., Braun, Daniela A., Gee, Heon Yung, McInerney-Leo, Aideen M., Krug, Pauline, Filhol, Emilie, Davis, Erica E., Airik, Rannar, Czarnecki, Peter G., Lehman, Anna M., Trnka, Peter, Nitschke, Patrick, Bole-Feysot, Christine, Schueler, Markus, Knebelmann, Bertrand, Burtey, Stephane, Szabo, Attila J., Tory, Kalman, Leo, Paul J., Gardiner, Brooke, McKenzie, Fiona A., Zankl, Andreas, Brown, Matthew A., Hartley, Jane L., Maher, Eamonn R., Li, Chunmei, Leroux, Michel R., Scambler, Peter J., Zhan, Shing H., Jones, Steven J., Kayserili, Hulya, Tuysuz, Beyhan, Moorani, Khemchand N., Constantinescu, Alexandru, Krantz, Ian D., Kaplan, Bernard S., Shah, Jagesh V., Hurd, Toby W., Doherty, Dan, Katsanis, Nicholas, Duncan, Emma L., Otto, Edgar A., Beales, Philip L., Mitchison, Hannah M., Saunier, Sophie and Hildebrandt, Friedhelm (2013) Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans. American Journal of Human Genetics, 93 5: 915-925. doi:10.1016/j.ajhg.2013.09.012

Urinary tract obstruction in the mouse: the kinetics of distal nephron injury

Hiatt, Michael J., Ivanova, Larissa, Trnka, Peter, Solomon, Marc and Matsell, Douglas G. (2013) Urinary tract obstruction in the mouse: the kinetics of distal nephron injury. Laboratory Investigation, 93 9: 1012-1023. doi:10.1038/labinvest.2013.90

Progressive multifocal leukoencephalopathy with gastrointestinal disease in a pediatric kidney transplant recipient

Burke, M. T., Trnka, P., Walsh, M., Poole, L., McTaggart, S. J. and Burke, J. R. (2013) Progressive multifocal leukoencephalopathy with gastrointestinal disease in a pediatric kidney transplant recipient. Pediatric Transplantation, 17 5: E119-E124. doi:10.1111/petr.12107

Congenital urinary tract obstruction: defining markers of developmental kidney injury

Trnka, Peter, Hiatt, Michael J., Tarantal, Alice F. and Matsell, Douglas G. (2012) Congenital urinary tract obstruction: defining markers of developmental kidney injury. Pediatric Research, 72 5: 446-454. doi:10.1038/pr.2012.113

Urinary biomarkers in obstructive nephropathy

Trnka, Peter, Ivanova, Larissa, Hiatt, Michael J. and Matsell, Douglas G. (2012) Urinary biomarkers in obstructive nephropathy. Clinical Journal of the American Society of Nephrology, 7 10: 1567-1575. doi:10.2215/CJN.09640911

Hypothesis: SLC12A3 polymorphism modifies thiazide hypersensitivity of antenatal Bartter syndrome to thiazide resistance

Mammen, Cherry, Rupps, Rosemarie, Trnka, Peter and Boerkoel, Cornelius F. (2012) Hypothesis: SLC12A3 polymorphism modifies thiazide hypersensitivity of antenatal Bartter syndrome to thiazide resistance. European Journal of Medical Genetics, 55 2: 96-98. doi:10.1016/j.ejmg.2011.12.006

Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy

Otto, Edgar A., Ramaswami, Gokul, Janssen, Sabine, Chaki, Moumita, Allen, Susan J., Zhou, Weibin, Airik, Rannar, Hurd, Toby W., Ghosh, Amiya K., Wolf, Matthias T., Hoppe, Bernd, Neuhaus, Thomas J., Bockenhauer, Detlef, Milford, David V., Soliman, Neveen A., Antignac, Corinne, Saunier, Sophie, Johnson, Colin A., Hildebrandt, Friedhelm, GPN Study Group and Trnka,Peter (2011) Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy. Journal of Medical Genetics, 48 2: 105-116. doi:10.1136/jmg.2010.082552

Co-occurence of Joubert Syndrome and Jeune Asphyxiating Thoracic Dystrophy

Lehman, A. M., Eydoux, E., Doherty, D., Glass, I. A., Chitayat, D., Hon-Yin, Chung B., Langlois, S., Yong, S. L., Lowry, B., Hildrebrandt, F. and Trnka, P. (2010) Co-occurence of Joubert Syndrome and Jeune Asphyxiating Thoracic Dystrophy. American Journal of Medical Genetics Part A, 152A 6: 1411-1419. doi:10.1002/ajmg.a.33416

Phenotypic transition of the collecting duct epithelium in congenital urinary tract obstruction

Trnka, Peter, Hiatt, Michael J., Ivanova, Larissa, Tarantal, Alice F. and Matsell, Douglas G. (2010) Phenotypic transition of the collecting duct epithelium in congenital urinary tract obstruction. Journal of Biomedicine and Biotechnology, 2010 . doi:10.1155/2010/696034

Selected primary care issues and comorbidities in children who are on maintenance dialysis: A review for the pediatric nephrologist

White, Colin Thomas, Trnka, Peter and Matsell, Douglas George (2007) Selected primary care issues and comorbidities in children who are on maintenance dialysis: A review for the pediatric nephrologist. Clinical Journal of The American Society of Nephrology, 2 4: 847-857. doi:10.2215/CJN.04021206

The Impact of Prematurity on Postnatal Renal Medulla Development

Li, Joan, Guandalini, Michael, Kandasamy, Joga, Moritz, Karen M. and Trnka, Peter (2017). The Impact of Prematurity on Postnatal Renal Medulla Development. In: Kidney Week, American Society of Nephrology, New Orleans, Louisiana, USA, (517-517). October 31 - November 5 2017.

Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic Nephropathy

Mallett, A., Mordaunt, D., Sonawane, R., Walker, A., Kausman, J., Peters, H., White, S., Stark, Z., Trnka, P., Patel, C., Crawford, J., Holman, K., Farnsworth, E., Ho, G., Alexander, S., Bennetts, B., Healy, H., Little, M., Simons, C. and Yaplito-Lee, J. (2015). Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic Nephropathy. In: Special Issue: 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology. 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, ACT Australia, (42-42). 7-9 September 2015. doi:10.1111/nep.12543

Outcome of primary focal segmental glomerulosclerosis in Australian and New Zealand pediatric renal transplant recipients

Francis, A., Trnka, P., Burke, J. R., Clayton, P. and McTaggart, S. J. (2014). Outcome of primary focal segmental glomerulosclerosis in Australian and New Zealand pediatric renal transplant recipients. In: 2014 World Transplant Congress, San Francisco CA, United States, (530-531). 26-31 July 2014.

Outcome of Primary Focal Segmental Glomerulosclerosis in Australian and New Zealand Pediatric Renal Transplant Recipients

Francis, Anna, Trnka, Peter, Burke, John R., Clayton, Philip and McTaggart, Steven J. (2013). Outcome of Primary Focal Segmental Glomerulosclerosis in Australian and New Zealand Pediatric Renal Transplant Recipients. In: IPNA Congress, Shanghai, China, (1517-1517). 30 August - 3 September 2013. doi:10.1007/s00467-013-2518-4

TRPV-4 deficiency inhibits apoptosis during urinary tract obstruction

Hiatt, M., Ivanova, L., Trnka, P. and Matsell, D. (2013). TRPV-4 deficiency inhibits apoptosis during urinary tract obstruction. In: Western Regional Meeting, Carmel, CA, United States, (221-221). 23–26 January 2013. doi:10.2310/JIM.0b013e31827d3ac9

The role of Y-box binding protein-1 in collecting duct epithelial-mesenchymal transition

Trnka, P., Ivanova, L., Hiatt, M. J., Dunn, S. E. and Matsell, D. G. (2010). The role of Y-box binding protein-1 in collecting duct epithelial-mesenchymal transition. In: 15th International Pediatric Nephrology Association Meeting, New York City, New York, USA, (1827-1827). 29 August - 2 September 2010.

Phenotypic transition of the human fetal obstructed duct epithelium

Trnka, P., Butt, M. J., Ivanova, L., Yoder, M. C., Tarantal, A. F. and Matsell, D. G. (2008). Phenotypic transition of the human fetal obstructed duct epithelium. In: Kidney Week, American Society of Nephrology, Philadelphia, PA, United States, (201A-201A). 4-9 November 2008.

Standardized surveillance of pediatric hemidialysis vascular access using an ultrasound dilution method

Mammen, C., Trnka, P., Paille, L., Heran, R., Robinson, A., Potts, J. and White, C. (2007). Standardized surveillance of pediatric hemidialysis vascular access using an ultrasound dilution method. In: 27th Annual Conference on Peritoneal Dialysis, 13th International Symposium on Hemodialysis, and 18th Annual Symposium on Pediatric Dialysis, Denver, Colorado, USA, (141-142). 18–20 February 2007.

Web calculators vs. inonic conductance vs. 1-URR

Mammen, C., Trnka, P., Paille, L., Heran, R., Robinson, A., Potts, J. and White, C. (2007). Web calculators vs. inonic conductance vs. 1-URR. In: 27th Annual Conference on Peritoneal Dialysis, Denver, Colorado, USA, (142-143). 18–20 February 2007.

Congenital urinary tract obstruction: linking form and function

Trnka, Peter (2010). Congenital urinary tract obstruction: linking form and function M.Sc Thesis, University of British Columbia.