Showing results (201-210 of 285) with videos related to
Sort By:
Pageof 29
Nephrologie|January 1, 1994
[Treatment of anemia in hemodialyzed children using recombinant human erythropoietin (Eprex). Results of a French multicenter clinical trial]M F Gagnadoux, C Loirat, J P Berthélémé, et al.Kidney International. Supplement|July 1, 1993
A specific glomerular lesion of the graft: allograft glomerulopathyR Habib, A Zurowska, N Hinglais, et al.Kidney International|April 1, 1995
Autosomal recessive Alport syndrome: immunohistochemical study of type IV collagen chain distributionM C Gubler, B Knebelmann, A Beziau, 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.Kidney International|October 1, 1978
Measurement of growth in children with renal insufficiencyD E Potter, M Broyer, C Chantler, et al.Archives Francaises De Pediatrie|June 1, 1984
[Association of early-onset nephrotic syndrome and microcephaly. Apropos of 4 cases in 2 families]J Gaudelus, G Leverger, G Rault, et al.Human Molecular Genetics|November 1, 1995
Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosisA Fuchshuber, G Jean, O Gribouval, et al.Archives Francaises De Pediatrie|August 1, 1985
[Pharmacokinetics of prednisone after oral administration in children with renal grafts. Changes induced by phenobarbital and renal insufficiency]F Perignon, M A Pecquinot, C Ged, et al.Kidney International|May 9, 1998
Crystalluria: a clinically useful investigation in children with primary hyperoxaluria post-transplantationP Jouvet, L Priqueler, M F Gagnadoux, et al.Clinical Nephrology|October 1, 1994
Evaluation in patients with Alport syndrome of knowledge of the disease and attitudes toward prenatal diagnosisM Levy, Y Pirson, P Simon, et al.Pageof 29