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Molecular Biomedicine|November 10, 2025
STAT3 regulates NK and NKT cell differentiation through C-X3-C motif chemokine receptor 1  (CX3CR1) in hyper-IgE syndromeJu Liu, Jingzhi Yang, Jianing Tang, et al.
European Journal of Medical Genetics|August 3, 2018
Renal tubular dysgenesis and microcolon, a novel association. Report of three casesAvi Saskin, Ahmed Alfares, Chantal Bernard, et al.
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.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 1, 2008
PAX3 is expressed in the stromal compartment of the developing kidney and in Wilms tumors with myogenic phenotypePierre-Alain Hueber, Ryuji Fukuzawa, Reyhan Elkares, 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.
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.
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