NEPHROLOGIE, UROLOGIE.

Por HAMBURGER, J., GRUNFELD, J-P, AUVERT, J.
Publicado em S1980

Nefrologia - Urologia /

Por Hamburger, J., Grunfeld, J. P., Rotellar, Jesus A. Oliver., Alvarez, T. A.
Publicado em 1973.

Recurrent rupture of intracranial aneurysms in autosomal dominant polycystic kidney disease.

Por Chauveau, D, Sirieix, M E, Schillinger, F, Legendre, C, Grünfeld, J P
Publicado em 1990

Immunoglobulin synthesis in primary and myeloma amyloidosis.

Por Preud'homme, J L, Ganeval, D, Grünfeld, J P, Striker, L, Brouet, J C
Publicado em 1988

Antineutrophil cytoplasmic antibodies (ANCA) directed against cathepsin G in ulcerative colitis, Crohn's disease and primary sclerosing cholangitis.

Por Halbwachs-Mecarelli, L, Nusbaum, P, Noël, L H, Reumaux, D, Erlinger, S, Grünfeld, J P, Lesavre, P
Publicado em 1992

Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-a...

Por Knebelmann, B, Deschenes, G, Gros, F, Hors, M C, Grünfeld, J P, Zhou, J, Tryggvason, K, Gubler, M C, Antignac, C
Publicado em 1992

Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.

Por Manouvrier, S, Rötig, A, Hannebique, G, Gheerbrandt, J D, Royer-Legrain, G, Munnich, A, Parent, M, Grünfeld, J P, Largilliere, C, Lombes, A
Publicado em 1995

Deletions in the COL4A5 collagen gene in X-linked Alport syndrome. Characterization of the pathological transcripts in nonrenal cells and correlation with disease expression.

Por Antignac, C, Knebelmann, B, Drouot, L, Gros, F, Deschênes, G, Hors-Cayla, M C, Zhou, J, Tryggvason, K, Grünfeld, J P, Broyer, M
Publicado em 1994

Effect of renal function on the pharmacokinetics and pharmacodynamics of trandolapril.

Por Bevan, E G, McInnes, G T, Aldigier, J C, Conte, J J, Grunfeld, J P, Harper, S J, Meyer, B H, Pauly, N, Wilkinson, R
Publicado em 1993

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.

Por Boye, E, Mollet, G, Forestier, L, Cohen-Solal, L, Heidet, L, Cochat, P, Grünfeld, J P, Palcoux, J B, Gubler, M C, Antignac, C
Publicado em 1998

Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome.

Por Knebelmann, B., Breillat, C., Forestier, L., Arrondel, C., Jacassier, D., Giatras, I., Drouot, L., Deschênes, G., Grünfeld, J. P., Broyer, M., Gubler, M. C., Antignac, C.
Publicado em 1996

Hypokalemic Periodic Paralysis and the Dihydropyridine Receptor (CACNLIA3): Genotype/Phenotype Correlations for two Predominant Mutations and Evidence for the Absence of a Founder...

Por Elbaz, A., Vale-Santos, J., Jurkat-Rott, K., Lapie, P., Ophoff, R. A., Bady, B., Links, T. P., Piussan, C., Vila, A., Monnier, N., Padberg, G. W., Abe, K., Feingold, N., Guimaraes, J., Wintzen, A. R., van der Hoeven, J. H., Saudubray, J. M., Grunfeld, J. P., Lenoir, G., Nivet, H., Echenne, B., Frants, R. R., Fardeau, M., Lehmann-Horn, F., Fontaine, B.
Publicado em 1995