M
Marion Valette
Researcher at French Institute of Health and Medical Research
Publications - 9
Citations - 290
Marion Valette is an academic researcher from French Institute of Health and Medical Research. The author has contributed to research in topics: Ghrelin & Medicine. The author has an hindex of 4, co-authored 6 publications receiving 205 citations.
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Journal ArticleDOI
The Use of Oxytocin to Improve Feeding and Social Skills in Infants With Prader-Willi Syndrome.
Maithé Tauber,Kader Boulanouar,Gwenaelle Diene,Sophie Çabal-Berthoumieu,Virginie Ehlinger,Pascale Fichaux-Bourin,Catherine Molinas,Sandy Faye,Marion Valette,Jeanne Pourrinet,Catie Cessans,Sylvie Viaux-Sauvelon,Céline Bascoul,Antoine Guedeney,Patric J.D. Delhanty,Vincent Geenen,Henri Martens,Françoise Muscatelli,David Cohen,Angèle Consoli,Pierre Payoux,Catherine Arnaud,Jean-Pierre Salles +22 more
TL;DR: OXT is well tolerated in infants with PWS and improves feeding and social skills and changes in circulating ghrelin and brain connectivity by functional MRI are documented.
Journal ArticleDOI
Melanocortin-4 receptor mutations and polymorphisms do not affect weight loss after bariatric surgery.
Marion Valette,Christine Poitou,Christine Poitou,Johanne Le Beyec,Jean-Luc Bouillot,Karine Clément,Karine Clément,Sébastien Czernichow +7 more
TL;DR: This is the first case-control study to show that MC4R mutations and polymorphisms do not affect weight loss and body composition over one year after bariatric surgery.
Journal ArticleDOI
Eating behaviour in obese patients with melanocortin-4 receptor mutations: a literature review.
Marion Valette,F. Bellisle,Claire Carette,Christine Poitou,Béatrice Dubern,Gilles Paradis,Serge Hercberg,Ludivine Muzard,Karine Clément,Sébastien Czernichow +9 more
TL;DR: This review examines the available literature on eating behaviours in carriers of MC4R mutations, and addresses binge eating disorder, bulimia nervosa, mealtime hyperphagia, snacking, psychological factors, satiety responsiveness and intake of energy and macro/micronutrient.
Journal ArticleDOI
Prader-Willi syndrome: A model for understanding the ghrelin system.
Maithé Tauber,Maithé Tauber,Muriel Coupaye,Gwenaelle Diene,Catherine Molinas,Catherine Molinas,Marion Valette,Véronique Beauloye +7 more
TL;DR: The current view of Prader‐Willi syndrome is presented, its natural history is explained, and recent data on the ghrelin system in PWS patients are discussed, to discuss the therapeutic approach of modulating the gh Relins system in these patients and the first promising results.
Journal ArticleDOI
Dyssynchrony and perinatal psychopathology impact of child disease on parents-child interactions, the paradigm of Prader Willi syndrom.
Sylvie Viaux-Savelon,Ouriel Rosenblum,Antoine Guedeney,Gwenaelle Diene,Sophie Çabal-Berthoumieu,Pascale Fichaux-Bourin,Catherine Molinas,Sandy Faye,Marion Valette,Céline Bascoul,David Cohen,Maithé Tauber +11 more
TL;DR: Dys-synchrony can be induced by children's pathology as well as parental pathology with emotional and developmental impact in the both cases and the PWS paradigm shows the necessity to sustain early parents-child relationship to avoid establishment of a negative transactional pattern of interaction.