Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Julie Galey"'
Autor:
Simone Perdigao-Cotta, Alexandra Pham-Scottez, Irema Barbosa-Magalhaes, Chrysoula Papastathi, Isabelle Nicolas, Claire Lamas, Sophie Christin-Maitre, Julie Galey, Maurice Corcos, Marie de Crecy
Publikováno v:
Eating and Weight Disorders - Studies on Anorexia, Bulimia and Obesity. 26:709-715
Relationships between weight and fertility are well known. The aim of this study is to assess the prevalence of lifetime eating disorder (ED) in a sample of infertile women seeking a specific infertility treatment, pulsatile gonadotropin-releasing ho
Autor:
Hady El Hachem, Nicolas Tabchouri, Adélie Michau, Bruno Guthauser, Cindy Guillaume, Mehdi Dahoun, Julie Galey, I. Hammoud, Simone Perdigao, Agathe Rousseau, Soizic le Parco
Publikováno v:
Journal of Gynecology Obstetrics and Human Reproduction. 48:811-815
The variability in indications and low rate of pregnancy compared to IVF have led many authors to dismiss IUI and offer IVF first-line instead.To determine what are the predictive factors for clinical pregnancy (CP) and live birth (LB) in intrauterin
Autor:
Isabelle Cedrin-Durnerin, Julie Galey-Fontaine, Nathalie Massin, Jean-Noël Hugues, Rachid Chaïbi
Publikováno v:
Reproductive BioMedicine Online. 10:94-99
The respective roles of age and ovarian reserve in predicting IVF outcome do not seem to be equivalent, as a high pregnancy rate seems to be preserved in the youngest women, despite low ovarian recruitment. The purpose of this study was to analyse th
Autor:
Nathalie di Clemente, Julie Galey, Paul Carmillo, Corinne Belville, Nathalie Josso, Jacques Gonzales, Jean-Yves Picard, Richard L. Cate, Gabrielle Machado, Laura Masgrau, Dominique Treton, Sophie Pennetier, Jean-Didier Maréchal, Liza Messika-Zeitoun
Publikováno v:
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2009, 18 (16), pp.3002-3013. ⟨10.1093/hmg/ddp238⟩
Human Molecular Genetics, 2009, 18 (16), pp.3002-3013. ⟨10.1093/hmg/ddp238⟩
Human Molecular Genetics, Oxford University Press (OUP), 2009, 18 (16), pp.3002-3013. ⟨10.1093/hmg/ddp238⟩
Human Molecular Genetics, 2009, 18 (16), pp.3002-3013. ⟨10.1093/hmg/ddp238⟩
International audience; The anti-Müllerian hormone type II (AMHRII) receptor is the primary receptor for anti-Müllerian hormone (AMH), a protein produced by Sertoli cells and responsible for the regression of the Müllerian duct in males. AMHRII is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86c7ca1980bb0a2a9e64e65b2c1d096a
https://hal.archives-ouvertes.fr/hal-01930692
https://hal.archives-ouvertes.fr/hal-01930692
Autor:
Julie Galey, Jean-Louis Bensimon, Christophe Pêcheux, Jean-Pierre Hardelin, Frédérique Kuttenn, Catherine Dodé, N. Massin, Corinne Eloit, Philippe Touraine
Publikováno v:
The Journal of clinical endocrinology and metabolism. 88(5)
Kallmann syndrome (KS) is characterized by the association of hypogonadotropic hypogonadism and anosmia. The gene underlying the X chromosome-linked form of the disease, KAL-1, consists of 14 coding exons. It encodes a glycoprotein, anosmin-1, which