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Canadian Journal of Kidney Health and Disease|February 13, 2020
Clinical Characteristics and Outcome of Canadian Patients Diagnosed With Atypical Hemolytic Uremic SyndromeAnne-Laure Lapeyraque, Martin Bitzan, Imad Al-Dakkak, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 16, 2014
Canadian Society of Nephrology Commentary on the 2012 KDIGO clinical practice guideline for glomerulonephritis: management of glomerulonephritis in adultsAndrey V Cybulsky, Michael Walsh, Greg Knoll, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 16, 2014
Canadian Society of Nephrology Commentary on the 2012 KDIGO clinical practice guideline for glomerulonephritis: management of nephrotic syndrome in childrenSusan Samuel, Martin Bitzan, Michael Zappitelli, et al.
Journal of Medical Genetics|February 26, 2013
ARHGDIA: a novel gene implicated in nephrotic syndromeIndra Rani Gupta, Cindy Baldwin, David Auguste, et al.
Molecular Biology of the Cell|January 23, 2015
Increased water flux induced by an aquaporin-1/carbonic anhydrase II interactionGonzalo Vilas, Devishree Krishnan, Sampath Kumar Loganathan, et al.
Pediatric Nephrology (Berlin, Germany)|August 7, 2013
Substantial practice variation exists in the management of childhood nephrotic syndromeSusan Samuel, Catherine J Morgan, Martin Bitzan, et al.
Pediatric Nephrology (Berlin, Germany)|July 3, 2008
Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndromeAndreas Dietrich, Verena Matejas, Martin Bitzan, et al.
Pediatric Nephrology (Berlin, Germany)|May 13, 2014
An audit analysis of a guideline for the investigation and initial therapy of diarrhea negative (atypical) hemolytic uremic syndromeSally Johnson, Jelena Stojanovic, Gema Ariceta, et al.
Canadian Journal of Kidney Health and Disease|May 12, 2015
The Canadian Childhood Nephrotic Syndrome (CHILDNEPH) Project: overview of design and methodsSusan Samuel, Shannon Scott, Catherine Morgan, et al.
Genome Medicine|May 23, 2022
Rapid whole genome sequencing of critically ill pediatric patients from genetically underrepresented populationsNour Halabi, Sathishkumar Ramaswamy, Maha El Naofal, et al.
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