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Pediatric Nephrology (Berlin, Germany)|November 5, 1997
Outcome of preemptive renal transplantation and pretransplantation dialysis in childrenA Mahmoud, M H Saïd, M Dawahra, et al.Human Molecular Genetics|January 1, 1995
Deletions of both alpha 5(IV) and alpha 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumoursL Heidet, K Dahan, J Zhou, et al.Human Genetics|February 1, 1991
Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locusM Berthelon, C Caillaud, F Rey, et al.Kidney International|November 1, 1992
Alport syndrome and diffuse leiomyomatosis: deletions in the 5' end of the COL4A5 collagen geneC Antignac, J Zhou, M Sanak, et al.European Journal of Pediatrics|December 22, 1999
Combined liver-kidney transplantation in primary hyperoxaluria type 1P Cochat, J M Gaulier, P C Koch Nogueira, et al.Journal of Inherited Metabolic Disease|January 1, 1993
2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new caseN Guffon, C Lopez-Mediavilla, R Dumoulin, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1995
Selection of transplantation procedures and perioperative management in primary hyperoxaluria type 1K Latta, N V Jamieson, J I Scheinman, et al.Journal De Genetique Humaine|January 1, 1989
[Contribution of molecular biology to the prevention of cystic fibrosis. Experience in Lyon]P Guibaud, M Auvinet, D Bozon, et al.Pediatric Nephrology (Berlin, Germany)|June 1, 1996
Body composition in children with renal disease: use of dual energy X-ray absorptiometryP Cochat, P Braillon, J Feber, et al.Pediatrie|January 1, 1991
[Resuscitation during renal transplantation in children]P Cochat, D Long, D Floret, et al.Pageof 32