Výsledky vyhledávání - "Frank Zinzindohoué"

One Thousand Single Anastomosis (Omega Loop) Gastric Bypasses to Treat Morbid Obesity in a 7-Year Period: Outcomes Show Few Complications and Good Efficacy

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6799f4eacbba5da8c66a8d1290bfabb7
https://doi.org/10.1007/s11695-014-1552-z

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SDHD immunohistochemistry : A new tool to validate SDHx mutations in pheochromocytoma/paraganglioma

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

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

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Syndrome d’Ehlers-Danlos vasculaire

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0ad9b117d97d26a8857b1230dd249f2c
https://doi.org/10.1016/s0755-4982(06)74919-3

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[Vascular Ehlers-Danlos syndrome]

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e539a9843369477ebc6e5a948c36bc70
https://pubmed.ncbi.nlm.nih.gov/17159712

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