Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Marie-Pierre Audrézet"'
Autor:
Annie Lahoche, Françoise Broux, Ferielle Louillet, Vincent Morinière, Olivia Boyer, Amélie Ryckenwaert, Hanitra Randrianaivo, Elodie Merieau, Said Lebbah, Stéphane Decramer, Marie-Pierre Audrézet, Djalila Mekahli, Sandrine Maestri, Laurence Heidet, Carine Abel, Christine Corbiere, Georges Deschênes, Claude Férec, Ines Ouertani, Rémi Salomon, Sylvie Cloarec, Emilie Cornec-Le Gall, Michel Fischbach, Véronique Baudouin, Chiara Visconti, Ariane Zaloszyc, Gwenaelle Roussey, Lucie Bessenay
Publikováno v:
Journal of the American Society of Nephrology. 27:722-729
Prenatal forms of autosomal dominant polycystic kidney disease (ADPKD) are rare but can be recurrent in some families, suggesting a common genetic modifying background. Few patients have been reported carrying, in addition to the familial mutation, v
Autor:
Dominique Besnier, Emilie Cornec-Le Gall, Didier Legrand, M.P. Morin, Marie-Pierre Audrézet, P. Jousset, Cécile Vigneau, Nazim Terki, E. Renaudineau, Régine Perrichot, Jerome Potier, Marie-Christine Moal, Theophile Sawadogo, Thierry Frouget, Christophe Charasse, Marie-Paule Guillodo, P. Siohan, Claude Férec, Hélène Longuet, Jacques Dantal, Seddik Benarbia, Annick Rousseau, Yannick Le Meur, Victorio Menoyo-Calonge, Bassem Wehbe, Maryvonne Hourmant
Publikováno v:
Journal of the American Society of Nephrology
Journal of the American Society of Nephrology, American Society of Nephrology, 2016, 27 (3), pp.942-951. ⟨10.1681/ASN.2015010016⟩
Journal of the American Society of Nephrology, 2016, 27 (3), pp.942-951. ⟨10.1681/ASN.2015010016⟩
Journal of the American Society of Nephrology, American Society of Nephrology, 2016, 27 (3), pp.942-951. ⟨10.1681/ASN.2015010016⟩
Journal of the American Society of Nephrology, 2016, 27 (3), pp.942-951. ⟨10.1681/ASN.2015010016⟩
International audience; The course of autosomal dominant polycystic kidney disease (ADPKD) varies among individuals, with some reaching ESRD before 40 years of age and others never requiring RRT. In this study, we developed a prognostic model to pred
Autor:
Marie-Pierre Audrézet, Hervé Gouérou, Michel Robaszkiewicz, Patrick Lozac'h, Jean-Paul Labat, Jean-Baptiste Nousbaum, Marie-Agnès Giroux, A. Volant, Claude Férec, Jean-Philippe Metges
Publikováno v:
European Journal of Gastroenterology & Hepatology. 14:15-18
Loss of heterozygosity (LOH) on chromosome 9 and p16 (MTS1/CDKN2) gene mutations have been reported in various human cancers. The present study aimed to determine the prevalence of LOH in 100 oesophageal squamous cell carcinomas (OSCCs) by typing mic
Autor:
Ingrid Duguépéroux, Michel Roussey, Virginie Scotet, Véronique David, Philippe Parent, Gilles Rault, Claude Férec, Michel Catheline, Marc De Braekeleer, Michel Dagorne, Jean-Pierre Codet, Auguste Lemoigne, C. Verlingue, Hubert Journel, Marie-Pierre Audrézet, Bernard Mercier, André Chaventré, Isabelle Quéré
Publikováno v:
Obstetric and Gynecologic Survey. 56:136-137
Summary Background Neonatal screening for cystic fibrosis has been a subject of debate over the past few years. This study assesses 10 years of neonatal screening in Brittany, France, and examines its impact on prenatal screening of subsequent pregna