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Kidney International. Supplement|July 1, 1993
A specific glomerular lesion of the graft: allograft glomerulopathyR Habib, A Zurowska, N Hinglais, et al.Archives Francaises De Pediatrie|November 1, 1991
[Hepatic and renal transplantation in the treatment of type I hyperoxaluria]P Jouvet, P Hubert, D Jan, et al.Human Genetics|January 1, 1987
Partial androgen receptor deficiency and mixed gonadal dysgenesis in Drash syndromeC Turleau, P Niaudet, C Sultan, et al.Human Pathology|August 1, 1992
Multicentric Kaposi's sarcoma in a 5-year-old human immunodeficiency virus-negative renal allograft recipientJ C Fournet, M Peuchmaur, P Eckart, et al.The Journal of Pediatrics|April 1, 1995
Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritisA Rötig, F Goutières, P Niaudet, et al.Pediatric Nephrology (Berlin, Germany)|January 17, 2002
Long term results of liver-kidney transplantation in children with primary hyperoxaluriaM F Gagnadoux, F Lacaille, P Niaudet, et al.Anales Espanoles De Pediatria|November 1, 1989
[Respiratory chain diseases in infancy. Clinical presentation and diagnosis]M T García Silva, J P Bonnefont, A Rotig, et al.Pediatrics|February 2, 1999
Hair and skin disorders as signs of mitochondrial diseaseC Bodemer, A Rötig, P Rustin, et al.American Journal of Human Genetics|March 1, 1996
High-resolution mapping of the gene for cystinosis, using combined biochemical and linkage analysisG Jean, A Fuchshuber, M M Town, et al.Nature Genetics|March 31, 2000
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndromeN Boute, O Gribouval, S Roselli, et al.Pageof 14