Mutation Analysis of NPHS1 in a Worldwide Cohort of Congenital Nephrotic Syndrome PatientsOVUNC, Bugsu; ASHRAF, Shazia; VEGA-WARNER, Virginia et al.The Nephron journals. 2012, Vol 120, Num 3, issn 1660-8151, c139-c146Article

Congenital disorders of glycosylation: a rare cause of nephrotic syndromeSINHA, Manish D; HORSFIELD, Catherine; KOMAROMY, Debbie et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 8, pp 2591-2594, issn 0931-0509, 4 p.Article

Therapy-resistant anaemia in congenital nephrotic syndrome of the Finnish type-implication of EPO, transferrin and transcobalamin lossesTOUBIANA, Julie; SCHLAGETER, Marie-Hélène; AOUN, Bilal et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 4, pp 1338-1340, issn 0931-0509, 3 p.Article

Nephrotic syndrome in the newbornFINN, Laura S; SYMONS, Jordan M; SMITH, Jodi M et al.American journal of kidney diseases. 2003, Vol 42, Num 6, pp 1318-1323, issn 0272-6386, 6 p.Article

Congenital nephrotic syndrome of finnish type : detection of new nephrin mutations and prenatal diagnosis in an italian familyGIGANTE, Maddalena; GRECO, Pantaleo; DEFAZIO, Vincenza et al.Prenatal diagnosis. 2005, Vol 25, Num 5, pp 407-410, issn 0197-3851, 4 p.Article

Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndromeFENCL, Filip; MALINA, Michal; STARA, Veronika et al.European journal of pediatrics. 2012, Vol 171, Num 1, pp 121-124, issn 0340-6199, 4 p.Article

Congenital nephrotic syndrome with adrenal calcification and cardiac malformationINDUMATHI, C. K; DINAKAR, Chitra; LEWIN, Sanjiv et al.Indian journal of pediatrics. 2005, Vol 72, Num 12, pp 1049-1051, issn 0019-5456, 3 p.Article

Management of congenital nephrotic syndromeKOVACEVIC, Larisa; REID, Christopher J. D; RIGDEN, Susan P. A et al.Pediatric nephrology (Berlin, West). 2003, Vol 18, Num 5, pp 426-430, issn 0931-041X, 5 p.Article

Neurodevelopmental deficits in pierson (microcoria-congenital nephrosis) syndromeWÜHL, Elke; KOGAN, Jillene; WEIS, Joachim et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 4, pp 311-319, issn 1552-4825, 9 p.Article

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: An autosomal recessive syndromeZENKER, Martin; TRALAU, Tim; LENNERT, Thomas et al.American journal of medical genetics. 2004, Vol 130A, Num 2, pp 138-145, issn 0148-7299, 8 p.Article

Prenatal findings in four consecutive pregnancies with fetal pierson syndrome, a newly defined congenital nephrosis syndromeMARK, Karlheinz; REIS, André; ZENKER, Martin et al.Prenatal diagnosis. 2006, Vol 26, Num 3, pp 262-266, issn 0197-3851, 5 p.Article