Mitochondrial disorders and the kidney

Por Niaudet, P.
Publicado em 1998

Thymic function in NZB mice. I. Duration of thymic function in New Zealand Black (NZB) mice

Por Niaudet, P., Bach, Marie-Anne
Publicado em 1976

Software and database for the analysis of mutations in the human WT1 gene.

Por Jeanpierre, C, Béroud, C, Niaudet, P, Junien, C
Publicado em 1998

In vitro characteristics on human lymphocyte functions of a new immunomodulatory agent, a cyclic peptide, cyclomunine.

Por Niaudet, P, Beaurain, G, Leibowitch, J, Bach, J F
Publicado em 1980

Systemic-onset juvenile rheumatoid arthritis and ANCA-associated glomerulonephritis

Por Belot, A, Bader-Meunier, B, Noel, LH, Prieur, AM, Niaudet, P, Salomon, R, Quartier, P
Publicado em 2008

Alteration of lung diffusion capacity in IgA nephropathy.

Por Ravilly, S, Chaussain, M, Iniguez, J L, Lenhert, A, Kalifa, G, Brun, P, Niaudet, P, Gendrel, D
Publicado em 1996

High-resolution mapping of the gene for cystinosis, using combined biochemical and linkage analysis.

Por Jean, G., Fuchshuber, A., Town, M. M., Gribouval, O., Schneider, J. A., Broyer, M., van't Hoff, W., Niaudet, P., Antignac, C.
Publicado em 1996

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized muta...

Por Jeanpierre, C, Denamur, E, Henry, I, Cabanis, M O, Luce, S, Cécille, A, Elion, J, Peuchmaur, M, Loirat, C, Niaudet, P, Gubler, M C, Junien, C
Publicado em 1998

Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations.

Por Lenkkeri, U, Männikkö, M, McCready, P, Lamerdin, J, Gribouval, O, Niaudet, P M, Antignac C, K, Kashtan, C E, Homberg, C, Olsen, A, Kestilä, M, Tryggvason, K
Publicado em 1999