検索結果 - Stéphanie Ngo
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Genetics and Outcome of Atypical Hemolytic Uremic Syndrome 著者: Véronique Frémeaux‐Bacchi, Fádi Fakhouri, Arnaud Garnier, Frank Bienaimé, Marie‐Agnès Dragon‐Durey, Stéphanie Ngo, Bruno Moulin, Aude Servais, François Provôt, Lionel Rostaing, Stéphane Burtey, Patrick Niaudet, Georges Deschênes, Yvon Lebranchu, Julien Zuber, Chantal Loirat
出版事項 2013Artigo -
2
Complement Factor B Mutations in Atypical Hemolytic Uremic Syndrome—Disease-Relevant or Benign? 著者: Maria Chiara Marinozzi, L Vergoz, Tania Rybkine, Stéphanie Ngo, Serena Bettoni, Anastas Pashov, Mathieu Cayla, Fanny Tabarin, Mathieu Jablonski, Christophe Hue, Richard J. Smith, Marina Noris, Lise Halbwachs‐Mecarelli, Roberta Donadelli, Véronique Frémeaux‐Bacchi, Lubka T. Roumenina
出版事項 2014Artigo -
3
Acquired and genetic complement abnormalities play a critical role in dense deposit disease and other C3 glomerulopathies 著者: Aude Servais, Laure‐Hélène Noël, Lubka T. Roumenina, Moglie Le Quintrec, Stéphanie Ngo, Marie‐Agnès Dragon‐Durey, Marie-Alice Macher, Julien Zuber, Alexandre Karras, François Provôt, Bruno Moulin, Jean‐Pierre Grünfeld, Patrick Niaudet, Philippe Lesavre, Véronique Frémeaux‐Bacchi
出版事項 2012Artigo
関連主題
Complement system
Immunology
Internal medicine
Medicine
Alternative complement pathway
Antibody
Atypical hemolytic uremic syndrome
Complement factor B
Factor H
Pathogenesis
Biology
C3-convertase
Disease
Focal segmental glomerulosclerosis
Gene
Genetics
Genotype
Glomerular basement membrane
Glomerulonephritis
Immune system
In silico
Intensive care medicine
Kidney
Membranoproliferative glomerulonephritis
Mesangial proliferative glomerulonephritis
Minimal change disease
Mutation
Pediatrics
Single-nucleotide polymorphism