Zobrazeno 1 - 10
of 123
pro vyhledávání: '"Muriel Coupaye"'
Comparison of pregnancy outcomes after bariatric surgery by sleeve gastrectomy versus gastric bypass
Autor:
Marie-Anne Joly, Violaine Peyronnet, Muriel Coupaye, Séverine Ledoux, Nicolas Pourtier, Lucile Pencole, Laurent Mandelbrot
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology: X, Vol 22, Iss , Pp 100309- (2024)
Objective: Bariatric surgery has an impact on subsequent pregnancies, in particular an association between gastric bypass and small for gestational age. Knowledge is lacking on whether sleeve gastrectomy is associated with more favorable pregnancy ou
Externí odkaz:
https://doaj.org/article/634050b77b0b4415a546657adf4a8990
Autor:
Laurence Salle, Olivier Foulatier, Muriel Coupaye, Vincent Frering, Alina Constantin, Anne-Sophie Joly, Ben Braithwaite, Fella Gharbi, Lysiane Jubin
Publikováno v:
Journal of Clinical Medicine, Vol 13, Iss 12, p 3519 (2024)
Background/Objectives: ACTION-FRANCE (Awareness, Care, and Treatment In Obesity maNagement in France) aims to identify the perceptions, attitudes, behaviors, and potential barriers to effective obesity management in France and guide collaborative act
Externí odkaz:
https://doaj.org/article/ee8605a7111a43dbb0d42ff20824df4c
Autor:
Cécile Louveau, Mimi-Caterina Turtulici, Angèle Consoli, Christine Poitou, Muriel Coupaye, Marie-Odile Krebs, Boris Chaumette, Anton Iftimovici
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
Externí odkaz:
https://doaj.org/article/230a08e439c24f9b943b97b09ae17dd6
Autor:
Cécile Louveau, Mimi-Caterina Turtulici, Angèle Consoli, Christine Poitou, Muriel Coupaye, Marie-Odile Krebs, Boris Chaumette, Anton Iftimovici
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
IntroductionPrader–Willi Syndrome (PWS) is a rare genetic condition, which affects one in 25,000 births and results in various phenotypes. It leads to a wide range of metabolic and endocrine disorders including growth delay, hypogonadism, narcoleps
Externí odkaz:
https://doaj.org/article/65941c8d6c9c48a8a595e55791afcfda
Autor:
Muriel Coupaye, Virginie Laurier, Grégoire Benvegnu, Christine Poitou, Pauline Faucher, Héléna Mosbah, Gwenaelle Diene, Graziella Pinto, Laura González Briceño, Christine Merrien, Ana Camarena Toyos, Emilie Montastier, Maithé Tauber, Fabien Mourre
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-8 (2021)
Abstract Background Patients with Prader-Willi syndrome (PWS) often have comorbidities, especially obesity, that may constitute a risk factor for severe forms of COVID-19. We aimed to assess prevalence and medical course of SARS-CoV-2 infection in ch
Externí odkaz:
https://doaj.org/article/8f58e7b845b34f7f87cd95a1188c91d4
Autor:
Helena Mosbah, Muriel Coupaye, Flavien Jacques, Maithé Tauber, Karine Clément, Jean-Michel Oppert, Christine Poitou
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-6 (2021)
Abstract Background Prader-Willi syndrome (PWS) is a neurodevelopmental disorder with hypothalamic dysfunction leading to obesity and behavioral disabilities, including eating disorders (EDs). We evaluated the effects of the COVID-19 infection and lo
Externí odkaz:
https://doaj.org/article/acb4bc1f46e44c99b70875d716be7757
Autor:
Muriel Coupaye, Lara Ribeiro-Parenti, Clément Baratte, Muriel Hourseau, Alexandra Willemetz, Henri Duboc, Séverine Ledoux, André Bado, Anne Couvelard, Maude Le Gall
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 5, p 1848 (2023)
Sleeve gastrectomy (SG) often induces gastroesophageal reflux, with few and discordant long-term data on the risk of Barrett’s esophagus (BE) in operated patients. The aim of this study was to analyze the impact of SG on esogastric mucosa in a rat
Externí odkaz:
https://doaj.org/article/583c9945d34246d49c4322f05b6f19b5
Autor:
Dibia Liz Pacoricona Alfaro, Perrine Lemoine, Virginie Ehlinger, Catherine Molinas, Gwénaëlle Diene, Marion Valette, Graziella Pinto, Muriel Coupaye, Christine Poitou-Bernert, Denise Thuilleaux, Catherine Arnaud, Maithé Tauber
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Abstract Background In the last 20 years, substantial improvements have been made in the diagnosis, treatment and management of patients with Prader-Willi syndrome (PWS). Few data on causes of death are available since those improvements were made. O
Externí odkaz:
https://doaj.org/article/27ec6559798c4c7590374449af42f65d
Autor:
Philippe Garteiser, Laurent Castera, Muriel Coupaye, Sabrina Doblas, Daniela Calabrese, Marco Dioguardi Burgio, Séverine Ledoux, Pierre Bedossa, Marina Esposito-Farèse, Simon Msika, Bernard E. Van Beers, Pauline Jouët
Publikováno v:
JHEP Reports, Vol 3, Iss 6, Pp 100381- (2021)
Background & Aims: Tools for the non-invasive diagnosis of non-alcoholic steatohepatitis (NASH) in morbidly obese patients with suspected non-alcoholic fatty liver disease (NAFLD) are an unmet clinical need. We prospectively compared the performance
Externí odkaz:
https://doaj.org/article/98a3d0f8ce494edc851fc058cba53761
Autor:
Pauline Dodet, Federica Sanapo, Smaranda Leu-Semenescu, Muriel Coupaye, Alice Bellicha, Isabelle Arnulf, Christine Poitou, Stefania Redolfi
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 7, p 1986 (2022)
Prader–Willi syndrome (PWS) is a rare, genetic, multisymptomatic, neurodevelopmental disease commonly associated with sleep alterations, including sleep-disordered breathing and central disorders of hypersomnolence. Excessive daytime sleepiness rep
Externí odkaz:
https://doaj.org/article/a5bc44c6f11b4af689c03eec19ba6543