Search Results - Patrick Niaudet
- Showing 1 - 20 results of 54
- Go to Next Page
-
1
-
2
Cyclosporine in the treatment of idiopathic nephrosis. by Patrick Niaudet, R Habib
Published 1994Revisão -
3
The kidney in mitochondrial cytopathies by Patrick Niaudet, Agnès Rötig
Published 1997Revisão -
4
-
5
Acute kidney injury complicating nephrotic syndrome of minimal change disease by A Meyrier, Patrick Niaudet
Published 2018Revisão -
6
Nephronophthisis by Rémi Salomon, Sophie Saunier, Patrick Niaudet
Published 2008Revisão -
7
-
8
-
9
-
10
NPHS2 mutation analysis shows genetic heterogeneityof steroid-resistant nephrotic syndrome and lowpost-transplant recurrence by Stefanie Weber, Olivier Gribouval, Ernie Esquivel, Vincent Morinière, Marie-Josèphe Tête, Christophe Legendre, Patrick Niaudet, Corinne Antignac
Published 2004Artigo -
11
-
12
-
13
-
14
-
15
Truncation of C-mip (Tc-mip), a New Proximal Signaling Protein, Induces c-maf Th2 Transcription Factor and Cytoskeleton Reorganization by Philippe Grimbert, Asta Valančiūtė, Vincent Audard, André Pawlak, Sabine Le gouvelo, Philippe Lang, Patrick Niaudet, A Bensman, Georges Guellaën, Dil Sahali
Published 2003Artigo -
16
-
17
Heterozygous and Homozygous Factor H Deficiencies Associated with Hemolytic Uremic Syndrome or Membranoproliferative Glomerulonephritis by Marie‐Agnès Dragon‐Durey, Véronique Frémeaux‐Bacchi, Chantal Loirat, Jacques Blouin, Patrick Niaudet, Georges Deschênes, Paul Coppo, Wolf H. Fridman, Laurence Weiss
Published 2004Artigo -
18
-
19
Effect of Plasma Protein Adsorption on Protein Excretion in Kidney-Transplant Recipients with Recurrent Nephrotic Syndrome by Jacques Dantal, Edith Bigot, Willy Bogers, Angelo Testa, Faiçal Kriaa, Yannick Jacques, Bruno Hurault de Ligny, Patrick Niaudet, Bernard Charpentier, Jean Paul Soulillou
Published 1994Artigo -
20
Genotype–Phenotype Correlations in Non-Finnish Congenital Nephrotic Syndrome by Eduardo Machuca, Geneviève Benoît, Fabien Névo, Marie-Josèphe Tête, Olivier Gribouval, Audrey Pawtowski, Per Brandström, Chantal Loirat, Patrick Niaudet, Marie‐Claire Gubler, Corinne Antignac
Published 2010Artigo
Search Tools:
Related Subjects
Medicine
Internal medicine
Kidney
Biology
Gene
Genetics
Endocrinology
Glomerulonephritis
Immunology
Mutation
Nephrotic syndrome
Proteinuria
Biochemistry
Chemistry
Gastroenterology
Pediatrics
Complement system
Disease
Pathology
Antibody
Urology
Focal segmental glomerulosclerosis
Phenotype
Transplantation
Atypical hemolytic uremic syndrome
Enzyme
Kidney disease
Missense mutation
Alternative complement pathway
Cysteamine