|
2015 Conference Publication Rmnd1 Mutations Are Associated with Autosomal Recessive Syndromic NephropathyMallett, 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. 51st Annual Scientific Meeting of the Australian and New Zealand Society of Nephrology, Canberra, ACT Australia, 7-9 September 2015. Richmond, VIC Australia: Wiley-Blackwell Publishing Asia. doi: 10.1111/nep.12543 |
|
2014 Journal Article Reninoma: an uncommon cause of renin-mediated hypertensionTrnka, Peter, Orellana, Luisa, Walsh, Mark, Pool, Louis and Borzi, Peter (2014). Reninoma: an uncommon cause of renin-mediated hypertension. Frontiers in Pediatrics, 2 (89) 89, 1-7. doi: 10.3389/fped.2014.00089 |
|
2014 Conference Publication Outcome of Primary Focal Segmental Glomerulosclerosis in Australian and New Zealand Renal Transplant RecipientsMcTaggart, S., Francis, A., Burke, J., Trnka, P. and Clayton, P. (2014). Outcome of Primary Focal Segmental Glomerulosclerosis in Australian and New Zealand Renal Transplant Recipients. World Transplant Congress, San Francisco, CA United States, 26-31 July 2014. Hoboken, NJ United States: Wiley-Blackwell. |
|
2014 Conference Publication Outcome of primary focal segmental glomerulosclerosis in Australian and New Zealand pediatric renal transplant recipientsFrancis, 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. 2014 World Transplant Congress, San Francisco, CA United States, 26-31 July 2014. Hoboken, NJ United States: Wiley-Blackwell. |
|
2013 Journal Article Henoch-Schonlein purpura in childrenTrnka, Peter (2013). Henoch-Schonlein purpura in children. Journal of Paediatrics and Child Health, 49 (12), 995-1003. doi: 10.1111/jpc.12403 |
|
2013 Journal Article Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in HumansHalbritter, 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 ... 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 |
|
2013 Journal Article Urinary tract obstruction in the mouse: the kinetics of distal nephron injuryHiatt, 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 |
|
2013 Journal Article Progressive multifocal leukoencephalopathy with gastrointestinal disease in a pediatric kidney transplant recipientBurke, 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 |
|
2013 Conference Publication Outcome of Primary Focal Segmental Glomerulosclerosis in Australian and New Zealand Pediatric Renal Transplant RecipientsFrancis, 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. IPNA Congress, Shanghai, China, 30 August - 3 September 2013. Heidelberg, Germany: Springer. doi: 10.1007/s00467-013-2518-4 |
|
2013 Conference Publication TRPV-4 deficiency inhibits apoptosis during urinary tract obstructionHiatt, M., Ivanova, L., Trnka, P. and Matsell, D. (2013). TRPV-4 deficiency inhibits apoptosis during urinary tract obstruction. Western Regional Meeting, Carmel, CA, United States, 23–26 January 2013. Philadelphia, PA, United States: Lippincott Williams & Wilkins. doi: 10.2310/JIM.0b013e31827d3ac9 |
|
2012 Journal Article Congenital urinary tract obstruction: defining markers of developmental kidney injuryTrnka, 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 |
|
2012 Journal Article Urinary biomarkers in obstructive nephropathyTrnka, 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 |
|
2012 Journal Article Hypothesis: SLC12A3 polymorphism modifies thiazide hypersensitivity of antenatal Bartter syndrome to thiazide resistanceMammen, 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 |
|
2011 Journal Article Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategyOtto, 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 |
|
2010 Other Outputs Congenital urinary tract obstruction: linking form and functionTrnka, Peter (2010). Congenital urinary tract obstruction: linking form and function. M.Sc Thesis, University of British Columbia. |
|
2010 Journal Article Co-occurence of Joubert Syndrome and Jeune Asphyxiating Thoracic DystrophyLehman, 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 |
|
2010 Journal Article Phenotypic transition of the collecting duct epithelium in congenital urinary tract obstructionTrnka, 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 696034. doi: 10.1155/2010/696034 |
|
2010 Conference Publication The role of Y-box binding protein-1 in collecting duct epithelial-mesenchymal transitionTrnka, 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. 15th International Pediatric Nephrology Association Meeting, New York City, New York, USA, 29 August - 2 September 2010. |
|
2008 Conference Publication Phenotypic transition of the human fetal obstructed duct epitheliumTrnka, 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. Kidney Week, American Society of Nephrology, Philadelphia, PA, United States, 4-9 November 2008. Washington, DC, United States: American Society Nephrology. |
|
2007 Journal Article Selected primary care issues and comorbidities in children who are on maintenance dialysis: A review for the pediatric nephrologistWhite, 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 |
