Zobrazeno 1 - 10
of 246
pro vyhledávání: '"G, Viot"'
Autor:
G. Viot, Jacques de Mouzon, Marie-José Gervoise-Boyer, Sylvie Epelboin, Fabienne Pessione, A. Devaux, Philippe Jonveaux, Patricia Fauque, Marianne Bergere, Morgane Valentin, Rachel Levy, Claire de Vienne
Publikováno v:
Human Reproduction. 36:808-816
STUDY QUESTIONDo IVF, IUI or female infertility (i.e. endometriosis, polycystic ovary syndrome [PCOS] and primary ovarian insufficiency [POI]) lead to an increased risk of congenital anomalies in singletons?SUMMARY ANSWERAfter multivariable adjustmen
Autor:
Morgane Valentin, Marie-José Gervoise-Boyer, Fabienne Pessione, Philippe Jonveaux, G. Viot, Rachel Levy, Sylvie Epelboin, Marianne Bergere, A. Deveaux, J. De Mouzon, C. Jimenez, F. Merlet
Publikováno v:
Gynécologie Obstétrique Fertilité & Sénologie. 48:351-358
Resume Objectifs L’objectif de cette etude etait de quantifier les risques de morbidite maternelle et perinatale en fecondation in vitro (FIV) par rapport aux grossesses non issues de FIV sur une cohorte nationale francaise recente. Methode Les don
Autor:
Marie-José Gervoise-Boyer, Morgane Valentin, Sylvie Epelboin, Claire de Vienne, Patricia Fauque, Philippe Jonveaux, G. Viot, A. Devaux, Jacques de Mouzon, Fabienne Pessione, Rachel Levy, Arianne Bergère
Publikováno v:
Clinical Epigenetics
Background Epidemiological studies suggest that singletons born from assisted reproductive technologies (ART) have a high risk of adverse perinatal outcomes, specifically for imprinting disorders. Because ART processes take place at times when epigen
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Autor:
F. Jacquemard, G. Viot
Publikováno v:
Gynécologie Obstétrique Fertilité & Sénologie. 45:50-53
Autor:
F, Pessione, J, De Mouzon, A, Deveaux, S, Epelboin, M-J, Gervoise-Boyer, C, Jimenez, R, Levy, M, Valentin, G, Viot, M, Bergère, F, Merlet, P, Jonveaux
Publikováno v:
Gynecologie, obstetrique, fertilitesenologie. 48(4)
The objective of this study was to quantify the risk of maternal and perinatal morbidity with in vitro fertilization (IVF) technology compared to non-IVF pregnancies in a recent French national cohort.The data was extracted from the hospital informat
Publikováno v:
Journal de Gynécologie Obstétrique et Biologie de la Reproduction. 45:1127-1132
Resume But Objectif : mettre en evidence la baisse du nombre de gestes invasifs intra-uterins grâce a l’analyse de l’ADN fœtoplacentaire libre circulant dans le sang maternel : le depistage prenatal non invasif (DPNI), au centre de diagnostic p
Autor:
Jérôme Le Bidois, Michel Tournaire, Emmanuel Devouche, Anne Cabau, G. Viot, Anne Levadou, Sylvie Epelboin, Annabel Dunbavand
Publikováno v:
Therapies. 71:395-404
Summary Objective Exposure to diethylstilbestrol (DES) in utero is associated with adverse health effects, including genital anomalies in women and men, and cancers in women. Animal studies showed birth defects and tumors in the offspring of DES expo
Autor:
Chloé Quélin, Linda Akloul, Véronique David, Christèle Dubourg, Sylvie Odent, Charlotte Mouden, Houda Hamdi-Rozé, H Salhi, G Viot, Valérie Dupé, Wilfrid Carré, Sophie Rose, P Darnault
Publikováno v:
Clinical Genetics. 89:659-668
Holoprosencephaly (HPE) is the most common congenital cerebral malformation, characterized by impaired forebrain cleavage and midline facial anomalies. Heterozygous mutations in 14 genes have been associated with HPE and are often inherited from an u
Autor:
Philippe Loget, Didier Lacombe, Marie-Pierre Cordier, Sébastien Moutton, Cyril Goizet, C. Abel, Cédric Hubert, Sophie Patrier, Julie Pilliod, G. Viot, Benoit Arveiler, Bettina Bessières, Alice Goldenberg, Julie Deforges, Isabelle Coupry, Caroline Rooryck, G. Sole, Anne-Lise Delezoide, Sophie Blesson, Patricia Fergelot, Elodie Guerineau, Alain Verloes, Judith Melki, F. Le Breton, S. Deves, Sophie Collardeau-Frachon, Sylvie Odent, Sophie Naudion
Publikováno v:
Clinical Genetics. 89:371-377
Otopalatodigital spectrum disorders (OPDSD) include OPD syndromes types 1 and type 2 (OPD1, OPD2), Melnick-Needles syndrome (MNS), and frontometaphyseal dysplasia (FMD). These conditions are clinically characterized by variable skeletal dysplasia ass