Hakutulokset - Geneviève Guest
- Näytetään 1 - 7 yhteensä 7 tuloksesta
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Cysteamine therapy delays the progression of nephropathic cystinosis in late adolescents and adults Tekijä Albane Brodin-Sartorius, Marie-Josèphe Tête, Patrick Niaudet, Corinne Antignac, Geneviève Guest, Chris Ottolenghi, Marina Charbit, Dominique Moyse, Christophe Legendre, Philippe Lesavre, Pierre Cochat, Aude Servais
Julkaistu 2011Artigo -
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Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome Tekijä Anne‐Laure Sellier‐Leclerc, Véronique Frémeaux‐Bacchi, Marie‐Agnès Dragon‐Durey, Marie-Alice Macher, Patrick Niaudet, Geneviève Guest, B. Boudailliez, F Bouissou, Georges Deschênes, Sophie Gié, Michel Tsimaratos, Michel Fischbach, Denis Morin, Hubert Nivet, Corinne Alberti, Chantal Loirat
Julkaistu 2007Artigo -
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Genetic and Functional Analyses of Membrane Cofactor Protein (CD46) Mutations in Atypical Hemolytic Uremic Syndrome Tekijä VeCombining Acute Accentronique Fremeaux-Bacchi, Elizabeth A. Moulton, David Kavanagh, Marie‐Agnès Dragon‐Durey, Jacques Blouin, Amy A. Caudy, Nadia Arzouk, Roxanna Cleper, Maud François, Geneviève Guest, Jacques Pourrat, Roland Seligman, Wolf H. Fridman, Chantal Loirat, John P. Atkinson
Julkaistu 2006Artigo -
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Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis Tekijä A. Godron, Jérôme Harambat, Valérie Boccio, A Mensire, Adrien May, Claire Rigothier, Lionel Couzi, Benoı̂t Barrou, M. Godin, Dominique Chauveau, Stanislas Faguer, Marion Vallet, Pierre Cochat, Philippe Eckart, Geneviève Guest, Vincent Guigonis, Pascal Houillier, Anne Blanchard, Xavier Jeunemaı̂tre, Rosa Vargas‐Poussou
Julkaistu 2012Artigo -
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Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum Can Be Caused by Mutations in Either ENPP1 or ABCC6 Tekijä Yvonne Nitschke, Geneviève Baujat, Ulrike Botschen, Tanja Wittkampf, Marcel du Moulin, Jacqueline Stella, Martine Le Merrer, Geneviève Guest, Karen Lambot, Marie-Frederique Tazarourte-Pinturier, Nicolas Chassaing, Olivier Roche, Ilse Feenstra, Karen J. Loechner, Charu Deshpande, Samuel J. Garber, Rashmi Chikarmane, Beat Steinmann, Tatevik Shahinyan, Loreto Martorell, Justin H. Davies, Wendy E. Smith, Stephen G. Kahler, Mignon McCulloch, Elizabeth Wraige, Lourdes Loidi, Wolfgang Höhne, Ludovic Martin, S. Hadj‐Rabia, Robert Terkeltaub, Frank Rutsch
Julkaistu 2011Artigo -
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The genetic landscape and clinical spectrum of nephronophthisis and related ciliopathies Tekijä Friederike Petzold, Katy Billot, Xiaoyi Chen, C. Henry, Emilie Filhol, Yoann Martin, Marina Avramescu, Maxime Douillet, Vincent Morinière, Pauline Krug, Marc Jeanpierre, Kálmán Tory, Olivia Boyer, Anita Burgun, Aude Servais, Rémi Salomon, Alexandre Benmerah, Laurence Heidet, Nicolas Garcelon, Corinne Antignac, Mohamad Zaidan, Sophie Saunier, Tania Attié‐Bitach, Valerie Comier-Daire, Jean‐Michel Rozet, Yaacov Frishberg, Brigitte Llanas, M. Broyer, Nabil Mohsin, Marie‐Alice Macher, Nicole Philip, Véronique Baudouin, D. Brackman, Chantal Loirat, Marina Charbit, Maud Dehennault, C. Guyot, Pierre Bataille, Mariet Elting, Georges Deschênes, Andrea Gropman, Geneviève Guest, Marie‐France Gagnadoux, Philippe Nicoud, Pierre Cochat, Bruno Ranchin, A Bensman, Anne‐Marie Guerrot, Bertrand Knebelmann, İlmay Bilge, Bruno Daniele, Stéphane Burtey, Caroline Rousset Rouvière, Valérie Caudwell, Denis Morin, Hélène Dollfus, Anne Maisin, Christian Hamel, Éric Bieth, Sophie Gié, Judith Goodship, G. Roussey, Hermine La Selve, Hubert Nivet, Lucie Bessenay, Mathilde Caillez, Jean Bernard Palcoux, Stéphane L. Benoit, Philippe Dubot, Marc Fila, Fabienne Giuliano, Daouya Iftene, M. Kessler, Thérèsa Kwon, A. Lahoche, Audrey Laurent, Anne-Laure Leclerc, David V. Milford, Thomas J. Neuhaus, Sylvie Odent, Philippe Eckart, Dominique Chauveau, Patrick Niaudet, Horacio A. Repetto, Sophie Taque, Alexandra Bruel, Alexandra Noel-Botte, Emma Allain Launay, Lisa Allard, Dany Anlicheau, Anne-Laure Adra, Arnaud Garnier, Arvind Nagra, Remy Baatard, Justine Bacchetta, Banu Sadıkoğlu, Christine Barnérias, Anne Barthélémy, Lina Basel, Nader Bassilios
Julkaistu 2023Artigo
Työkalut:
Liittyvät aiheet
Medicine
Internal medicine
Biology
Gene
Genetics
Disease
Mutation
Pediatrics
Phenotype
Antibody
Atypical hemolytic uremic syndrome
CD46
Complement factor I
Complement system
Endocrinology
Factor H
Gastroenterology
Immunology
Transplantation
Age of onset
Alternative complement pathway
Bardet–Biedl syndrome
Biochemistry
Calcification
Calcium
Chemistry
Ciliogenesis
Ciliopathies
Ciliopathy
Cilium