Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Frank Zinzindohoué"'
Autor:
Nathan Beaupel, Martino Guenzi, Anne Berger, Gustavo A. Arman, Jean Marc Chevallier, Cedric Rau, Mathieu Bruzzi, Frank Zinzindohoué
Publikováno v:
Obesity Surgery. 25:951-958
A short-term randomized controlled trial shows that the one anastomosis gastric bypass (OAGB) is a safe and effective alternative to the Roux-en-Y gastric bypass (RYGB). The aim of this study is to evaluate the OAGB at our University Hospital between
Autor:
Anne Paule Gimenez-Roqueplo, Judith Favier, Lindsey Oudijk, Cécile Badoual, Frank Zinzindohoué, Ronald R. de Krijger, Mathilde Sibony, Xavier Iturrioz, Mélanie Menara, Jérôme Bertherat, Laurence Amar, Charlotte Lepoutre-Lussey
Publikováno v:
Journal of Clinical Endocrinology and Metabolism, 100(2), E287-E291. Endocrine Society
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2015, 100 (2), pp.E287-E291. ⟨10.1210/jc.2014-1870⟩
Journal of Clinical Endocrinology and Metabolism, 100(2), E287. The Endocrine Society
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, Endocrine Society, 2015, 100 (2), pp.E287-E291. ⟨10.1210/jc.2014-1870⟩
Journal of Clinical Endocrinology and Metabolism, 100(2), E287. The Endocrine Society
Context: Pheochromocytomas (PCC) and paragangliomas (PGL) may be caused by a germline mutation in 12 different predisposing genes. We previously reported that immunohistochemistry is a useful approach to detect patients harboring SDHx mutations. SDHA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4925a3d3382abf844cfc38b10e844043
https://dspace.library.uu.nl/handle/1874/349925
https://dspace.library.uu.nl/handle/1874/349925
Autor:
Jérôme Perdu, Philippe Khau Van Kien, Jean-Noël Fiessinger, Khadija Lahlou-Laforêt, Denis Trystram, Marc Sapoval, Nicolas Denarié, Pierre Julia, Anne-Paule Gimenez-Roqueplo, Frank Zinzindohoué, Elie Mousseaux, Yves Dumez, Xavier Jeunemaitre, Catherine Vignal-Clermont, Pierre Boutouyrie, Philippe Touraine
Publikováno v:
La Presse Médicale. 35:1864-1875
Points essentiels Le syndrome d’Ehlers-Danlos (SED) vasculaire est une maladie genetique rare de transmission autosomique dominante. Il se distingue des autres formes de SED par un morphotype acrogerique inconstant et par la survenue de complicatio
Autor:
Jérôme, Perdu, Pierre, Boutouyrie, Khadija, Lahlou-Laforêt, Philippe, Khau Van Kien, Nicolas, Denarié, Elie, Mousseaux, Marc, Sapoval, Pierre, Julia, Frank, Zinzindohoué, Philippe, Touraine, Yves, Dumez, Denis, Trystram, Catherine, Vignal-Clermont, Anne-Paule, Gimenez-Roqueplo, Xavier, Jeunemaitre, Jean-Noël, Fiessinger
Publikováno v:
Presse medicale (Paris, France : 1983). 35(12 Pt 2)
The vascular type of Ehlers-Danlos syndrome (EDS) is a rare genetic disease transmitted as an autosomal dominant trait. It is distinguished from other forms of EDS by its unstable acrogeric morphotype and by vascular, gastrointestinal, and obstetrica
Autor:
Sakran N; Assuta Medical Center, Tel Aviv, Israel.; Department of General Surgery, Holy Family Hospital, Nazareth, Israel.; The Azrieli Faculty of Medicine Safed, Bar-Ilan University, Ramat Gan, Israel., Raziel A; Assuta Medical Center, Tel Aviv, Israel., Hod K; Assuta Medical Center, Tel Aviv, Israel., Azaria B; Assuta Medical Center, Tel Aviv, Israel., Kaplan U; Assuta Medical Center, Tel Aviv, Israel.; Department of Surgery, Emek Medical Center, Afula, Israel.; Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
Publikováno v:
World journal of surgery [World J Surg] 2024 Jun; Vol. 48 (6), pp. 1458-1466. Date of Electronic Publication: 2024 Apr 09.
Autor:
Chevallier, Jean, Arman, Gustavo, Guenzi, Martino, Rau, Cedric, Bruzzi, Mathieu, Beaupel, Nathan, Zinzindohoué, Frank, Berger, Anne
Publikováno v:
Obesity Surgery; Jun2015, Vol. 25 Issue 6, p951-958, 8p