Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Alfons Garcia-Piñero"'
Autor:
Michel Pugeat, Charlotte Vanacker, Christine Cortet-Rudelli, Vincent Meyer, Corinne Fouveaut, Céline Campagne, Catherine Dodé, Chrystel Leroy, Stéphanie Baron, Gérard Chabrier, Jyoti Parkash, Alfons Garcia-Piñero, Vincent Prevot, Paolo Giacobini, Ksenija Gersak, Chantal Metz, Francis Collier, Cécile Espy, Jacques Young, J.-P. Hardelin, Didier Dewailly, Pierre Lhuillier, Naresh Kumar Hanchate, Corinne Cruaud
Publikováno v:
PLoS Genetics
PLoS Genetics, 2012, 8 (8), pp.e1002896. ⟨10.1371/journal.pgen.1002896⟩
PLoS Genetics, Public Library of Science, 2012, 8 (8), pp.e1002896. ⟨10.1371/journal.pgen.1002896⟩
PLoS Genetics, Vol 8, Iss 8, p e1002896 (2012)
PLoS Genetics, 2012, 8 (8), pp.e1002896. ⟨10.1371/journal.pgen.1002896⟩
PLoS Genetics, Public Library of Science, 2012, 8 (8), pp.e1002896. ⟨10.1371/journal.pgen.1002896⟩
PLoS Genetics, Vol 8, Iss 8, p e1002896 (2012)
Kallmann syndrome (KS) associates congenital hypogonadism due to gonadotropin-releasing hormone (GnRH) deficiency and anosmia. The genetics of KS involves various modes of transmission, including oligogenic inheritance. Here, we report that Nrp1 sema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a2a520d6b7ae98e8c17e461b664bc8e
https://www.hal.inserm.fr/inserm-03204465/file/pgen.1002896.pdf
https://www.hal.inserm.fr/inserm-03204465/file/pgen.1002896.pdf
Autor:
Slawomir Wolczynski, Thierry Brue, Claire Bouvattier, Philippe Rondard, Isabelle Arnulf, Anne Guiochon-Mantel, F. Despert, Sylvie Cabrol, Paolo Tonella, Philippe Bouchard, Maria Ramos-Arroyo, Jean-Pierre Hardelin, Sylvie Brailly-Tabard, Michèle Mathieu, Jacques Young, Catherine Dodé, Gérard Reach, Graeme Morgan, Nathalie Chabbert-Buffet, Alfons Garcia-Piñero, James Lespinasse, Nicole De Talence, Arnaud Murat, Sébastien Jacquemont, Julie Sarfati, Bruno Delobel, Catherine Bremont, Anne Lienhardt-Roussie, Zinet Turki, Maud Bidet, Michel Pugeat, Hélène Du Boullay, Bernard Conrad
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2010, 95 (2), pp.659-69. ⟨10.1210/jc.2009-0843⟩
Journal of Clinical Endocrinology and Metabolism, 2010, 95 (2), pp.659-69. ⟨10.1210/jc.2009-0843⟩
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2010, 95 (2), pp.659-69. ⟨10.1210/jc.2009-0843⟩
Journal of Clinical Endocrinology and Metabolism, 2010, 95 (2), pp.659-69. ⟨10.1210/jc.2009-0843⟩
International audience; Context: Both biallelic and monoallelic mutations in PROK2 or PROKR2 have been found in Kallmann syndrome (KS). Objective: The objective of the study was to compare the phenotypes of KS patients harboring monoallelic and biall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4870f9553c8bb28f082e878bd54986fd
https://pubmed.ncbi.nlm.nih.gov/20022991
https://pubmed.ncbi.nlm.nih.gov/20022991
Autor:
Naresh Kumar Hanchate, Paolo Giacobini, Pierre Lhuillier, Jyoti Parkash, Cécile Espy, Corinne Fouveaut, Chrystel Leroy, Stéphanie Baron, Céline Campagne, Charlotte Vanacker, Francis Collier, Corinne Cruaud, Vincent Meyer, Alfons García-Piñero, Didier Dewailly, Christine Cortet-Rudelli, Ksenija Gersak, Chantal Metz, Gérard Chabrier, Michel Pugeat, Jacques Young, Jean-Pierre Hardelin, Vincent Prevot, Catherine Dodé
Publikováno v:
PLoS Genetics, Vol 8, Iss 8, p e1002896 (2012)
Kallmann syndrome (KS) associates congenital hypogonadism due to gonadotropin-releasing hormone (GnRH) deficiency and anosmia. The genetics of KS involves various modes of transmission, including oligogenic inheritance. Here, we report that Nrp1(sema
Externí odkaz:
https://doaj.org/article/c1e81f5391e44f4ab20b6d919cff8aa2