Výsledky vyhledávání - Hubert Nivet
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Reversed polarized delivery of an aquaporin-2 mutant causes dominant nephrogenic diabetes insipidus Autor Erik‐Jan Kamsteeg, Daniel G. Bichet, Irene B. M. Konings, Hubert Nivet, Michelle Lonergan, Marie‐Françoise Arthus, C.H. van Os, Peter M.T. Deen
Vydáno 2003Artigo -
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Early Pulse Pressure and Low-Grade Proteinuria as Independent Long-Term Risk Factors for New-Onset Diabetes Mellitus After Kidney Transplantation Autor M. Roland, Philippe Gatault, A. Al-Najjar, Claire Doute, Isabelle Barbet, Valérie Châtelet, J. Marlière, Hubert Nivet, M.W. Büchler, Yvon Lebranchu, J.M. Halimi, I. Laouad
Vydáno 2008Artigo -
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Focal scar and diffuse myocardial fibrosis are independent imaging markers in repaired tetralogy of Fallot Autor Hubert Cochet, Xavier Iriart, Antoine Allain-Nicolaï, Claudia Camaioni, Soumaya Sridi, Hubert Nivet, Emmanuelle Fournier, Marie–Lou Dinet, Zakaria Jalal, François Laurent, Michel Montaudon, Jean‐Benoît Thambo
Vydáno 2019Artigo -
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High-Resolution Late Gadolinium Enhancement Magnetic Resonance for the Diagnosis of Myocardial Infarction With Nonobstructed Coronary Arteries Autor Pierre-François Lintingre, Hubert Nivet, Stéphanie Clément-Guinaudeau, Claudia Camaioni, Soumaya Sridi, O. Corneloup, Édouard Gerbaud, Pierre Coste, Gaël Dournes, V. Latrabe, François Laurent, Michel Montaudon, Hubert Cochet
Vydáno 2020Artigo -
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OCT and CMR for the Diagnosis of Patients Presenting With MINOCA and Suspected Epicardial Causes Autor Édouard Gerbaud, Fabien Arabucki, Hubert Nivet, Christophe Barbey, Laura Cetran, Stéphan Chassaing, Benjamin Séguy, Arnaud Lesimple, Hubert Cochet, Michel Montaudon, François Laurent, Olivier Bar, Guillermo J. Tearney, Pierre Coste
Vydáno 2020Artigo -
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Death after withdrawal from dialysis: the most common cause of death in a French dialysis population Autor Béatrice Birmelé, François Mullier, J Pengloan, Patrick Français, Didier Testou, G Brillet, D. Lechapois, S. Baudin, O. Grézard, Jean-Louis Jourdan, M. Fodil-Cherif, Mona Abaza, L Dupouet, Gilles Fournier, Hubert Nivet
Vydáno 2004Artigo -
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Mutations of NPHP2 and NPHP3 in infantile nephronophthisis Autor Kálmán Tory, Caroline Rousset‐Rouvière, Marie‐Claire Gubler, Vincent Morinière, Audrey Pawtowski, C. Becker, C. Guyot, Sophie Gié, Yaacov Frishberg, Hubert Nivet, Georges Deschênes, Pierre Cochat, Marie‐France Gagnadoux, Sophie Saunier, Corinne Antignac, Rémi Salomon
Vydáno 2009Artigo -
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Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome Autor Jérôme Harambat, Sonia Fargue, Cécile Acquaviva, Marie‐France Gagnadoux, Françoise Janssen, A. Liutkus, Chebl Mourani, Marie‐Alice Macher, Daniel Abramowicz, Christophe Legendre, Antoine Dürrbach, Michel Tsimaratos, Hubert Nivet, Éric Girardin, Anne‐Marie Schott, Marie-Odile Rolland, Pierre Cochat
Vydáno 2009Artigo -
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Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1 Autor Sonia Fargue, Jérôme Harambat, Marie‐France Gagnadoux, Michel Tsimaratos, Françoise Janssen, Brigitte Llanas, Jean-Pierre Berthélémé, B. Boudailliez, Gérard Champion, C. Guyot, Marie‐Alice Macher, Hubert Nivet, Bruno Ranchin, Rémi Salomon, Sophie Taque, Marie-Odile Rolland, Pierre Cochat
Vydáno 2009Artigo -
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Differential Impact of Complement Mutations on Clinical Characteristics in Atypical Hemolytic Uremic Syndrome Autor 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
Vydáno 2007Artigo -
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Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide study Autor Anne‐Sylvia Sacri, T. Chambaraud, Bruno Ranchin, Benoît Florkin, H. See, Stéphane Decramer, Hugues Flodrops, Tim Ulinski, Emma Allain‐Launay, Olivia Boyer, Olivier Dunand, Michel Fischbach, É. Hachulla, Christine Piétrement, P. Le Pogamp, JL Stéphan, Alexandre Bélot, Hubert Nivet, François Nobili, Loı̈c Guillevin, Pierre Quartier, Georges Deschênes, Rémi Salomon, Marie Essig, J. Harambat
Vydáno 2015Artigo -
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Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination Autor Edgar A. Otto, Bernhard Schermer, Tomoko Obara, John F. O’Toole, Karl S. Hiller, Adelheid M. Mueller, Rainer Ruf, Julia Hoefele, Frank Beekmann, Daniel Landau, John W. Foreman, Judith A. Goodship, Tom Strachan, Andreas Kispert, Matthias T. F. Wolf, M. F. Gagnadoux, Hubert Nivet, Corinne Antignac, Gerd Walz, Iain A. Drummond, Thomas Benzing, Friedhelm Hildebrandt
Vydáno 2003Artigo -
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Spectrum of Mutations in Gitelman Syndrome Autor Rosa Vargas‐Poussou, Karin Dahan, Diana Kahila, Annabelle Vénisse, Eva Riveira‐Muñoz, Huguette Debaix, Bernard Grisart, Frank Bridoux, Robert J. Unwin, Bruno Moulin, Jean‐Philippe Haymann, Marie‐Christine Vantyghem, Claire Rigothier, Bertrand Dussol, M. Godin, Hubert Nivet, Laurence Dubourg, Ivan Tack, Anne‐Paule Gimenez‐Roqueplo, Pascal Houillier, Anne Blanchard, Olivier Devuyst, Xavier Jeunemaı̂tre
Vydáno 2011Artigo -
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Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome Autor Véronique Frémeaux‐Bacchi, Elizabeth C. Miller, M. Kathryn Liszewski, Lisa Strain, Jacques Blouin, Alison L. Brown, Nadeem Moghal, Bernard S. Kaplan, Robert A. Weiss, Karl Lhotta, Gaurav Kapur, Tej K. Mattoo, Hubert Nivet, William Wong, Sophie Gié, Bruno Hurault de Ligny, Michel Fischbach, Ritu Gupta, Richard E. Hauhart, Vincent Meunier, Chantal Loirat, Marie‐Agnès Dragon‐Durey, Wolf H. Fridman, B.J.C. Janssen, Timothy H.J. Goodship, John P. Atkinson
Vydáno 2008Artigo -
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Mutation Update of the<i>CLCN5</i>Gene Responsible for Dent Disease 1 Autor Lamisse Mansour‐Hendili, Anne Blanchard, Nelly Le Pottier, Isabelle Roncelin, Stéphane Lourdel, Cyrielle Tréard, Wendy González, Ariela Vergara‐Jaque, Gilles Morin, Estelle Colin, Muriel Holder‐Espinasse, Justine Bacchetta, Véronique Baudouin, Stéphane L. Benoit, E. Bérard, Guylhène Bourdat-Michel, Karim Bouchireb, Stéphane Burtey, Mathilde Cailliez, Gérard Cardon, C. Cartery, Gérard Champion, Dominique Chauveau, Pierre Cochat, Karin Dahan, Renaud de la Faille, François-Guillaume Debray, Laurenne Dehoux, Georges Deschênes, Éstelle Desport, Olivier Devuyst, Stella M. Dieguez, Francesco Emma, Michel Fischbach, Denis Fouque, Jacques Fourcade, Arnaud François, Brigitte Gilbert‐Dussardier, Thierry Hannedouche, Pascal Houillier, Hassan Izzedine, Marco Janner, Alexandre Karras, Bertrand Knebelmann, Marie-Pierre Lavocat, Sandrine Lemoine, Valériane Leroy, Chantal Loirat, Marie-Alice Macher, Dominique Martin–Coignard, Denis Morin, Patrick Niaudet, Hubert Nivet, François Nobili, Robert Novo, Laurence Faivre, Claire Rigothier, Gwénaëlle Roussey-Kesler, Rémi Salomon, Andreas Schleich, A.L. Sellier-Leclerc, Kenza Soulami, A. Tiple, Tim Ulinski, Philippe Vanhille, Nicole Van Regemorter, Xavier Jeunemaı̂tre, Rosa Vargas‐Poussou
Vydáno 2015Revisão
Vyhledávací nástroje:
Související témata
Medicine
Internal medicine
Biology
Gene
Genetics
Kidney
Mutation
Disease
Phenotype
Radiology
Antibody
Cardiology
Endocrinology
Immunology
Surgery
Atypical hemolytic uremic syndrome
Complement system
Gastroenterology
Kidney disease
Nephronophthisis
Retrospective cohort study
Alternative complement pathway
Anti-neutrophil cytoplasmic antibody
Autoantibody
Cilium
Cohort
Complement factor I
Creatinine
Cystic kidney disease
Diabetes mellitus