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Pediatrics|July 5, 2005
Factitious hyperinsulinism leading to pancreatectomy: severe forms of Munchausen syndrome by proxyIrina Giurgea, Tim Ulinski, Guy Touati, et al.Pediatric Nephrology (Berlin, Germany)|July 5, 2021
To biopsy or not to biopsy: Henoch-Schönlein nephritis in children, a 5-year follow-up studyMarina Avramescu, Annie Lahoche, Julien Hogan, et al.Pediatric Nephrology (Berlin, Germany)|May 7, 2008
Stem cell mobilization in idiopathic steroid-sensitive nephrotic syndromeHélène Lapillonne, Annelaure Leclerc, Tim Ulinski, et al.Human Mutation|September 17, 2011
Two mutations in human BICC1 resulting in Wnt pathway hyperactivity associated with cystic renal dysplasiaMarine R-C Kraus, Séverine Clauin, Yvan Pfister, et al.Pediatric Nephrology (Berlin, Germany)|November 8, 2019
Histological prognostic factors in children with Henoch-Schönlein purpura nephritisJean-Daniel Delbet, Guillaume Geslain, Martin Auger, et al.Journal of the American Society of Nephrology : JASN|July 20, 2001
Transcriptional and post-transcriptional alterations of IkappaBalpha in active minimal-change nephrotic syndromeDjillali Sahali, André Pawlak, Sabine LE Gouvello, et al.The Journal of Experimental Medicine|August 27, 2003
Truncation of C-mip (Tc-mip), a new proximal signaling protein, induces c-maf Th2 transcription factor and cytoskeleton reorganizationPhilippe Grimbert, Asta Valanciute, Vincent Audard, et al.Journal of the American Society of Nephrology : JASN|February 13, 2010
Phenotype and genotype characterization of adenine phosphoribosyltransferase deficiencyGuillaume Bollée, Cécile Dollinger, Lucile Boutaud, et al.British Journal of Clinical Pharmacology|April 22, 2010
Population pharmacokinetics and Bayesian estimator of mycophenolic acid in children with idiopathic nephrotic syndromeWei Zhao, Valéry Elie, Véronique Baudouin, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 29, 2014
Acute metabolic acidosis in a GLUT2-deficient patient with Fanconi-Bickel syndrome: new pathophysiology insightsFabrice Mihout, Olivier Devuyst, Albert Bensman, et al.Pageof 15