Marion Valette
Marion Valette
Research associate, Prader-Willi Reference Center, Pediatric endocrinology unit, CHU Toulouse, TMBI
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Cited by
Cited by
Melanocortin-4 receptor mutations and polymorphisms do not affect weight loss after bariatric surgery
M Valette, C Poitou, J Le Beyec, JL Bouillot, K Clement, S Czernichow
PloS one 7 (11), e48221, 2012
The use of oxytocin to improve feeding and social skills in infants with Prader–Willi syndrome
M Tauber, K Boulanouar, G Diene, S Çabal-Berthoumieu, V Ehlinger, ...
Pediatrics 139 (2), 2017
Eating behaviour in obese patients with melanocortin-4 receptor mutations: a literature review
M Valette, F Bellisle, C Carette, C Poitou, B Dubern, G Paradis, ...
International journal of obesity 37 (8), 1027-1035, 2013
Casein compared with whey proteins affects the organization of dietary fat during digestion and attenuates the postprandial triglyceride response to a mixed high-fat meal in …
F Mariotti, M Valette, C Lopez, H Fouillet, MH Famelart, V Mathé, G Airinei, ...
The Journal of nutrition 145 (12), 2657-2664, 2015
Association between melanocortin-4 receptor mutations and eating behaviors in obese patients: a case–control study
M Valette, C Poitou, E Kesse-Guyot, F Bellisle, C Carette, J Le Beyec, ...
International journal of obesity 38 (6), 883-885, 2014
Causes of death in Prader-Willi syndrome: lessons from 11 years’ experience of a national reference center
DLP Alfaro, P Lemoine, V Ehlinger, C Molinas, G Diene, M Valette, ...
Orphanet journal of rare diseases 14 (1), 1-10, 2019
Modeling a real-case situation of egress using BDI agents with emotions and social skills
M Valette, B Gaudou, D Longin, P Taillandier
International Conference on Principles and Practice of Multi-Agent Systems, 3-18, 2018
Prader‐Willi syndrome: A model for understanding the ghrelin system
M Tauber, M Coupaye, G Diene, C Molinas, M Valette, V Beauloye
Journal of neuroendocrinology 31 (7), e12728, 2019
Face processing and exploration of social signals in Prader-Willi syndrome: a genetic signature
J Debladis, M Valette, K Strenilkov, C Mantoulan, D Thuilleaux, V Laurier, ...
Orphanet journal of rare diseases 14 (1), 262, 2019
Dyssynchrony and perinatal psychopathology impact of child disease on parents-child interactions, the paradigm of Prader Willi syndrom
S Viaux-Savelon, O Rosenblum, A Guedeney, G Diene, ...
Journal of Physiology-Paris 110 (4), 427-433, 2016
A study of voice and non-voice processing in Prader-Willi syndrome
K Strenilkov, J Debladis, J Salles, M Valette, C Mantoulan, D Thuilleaux, ...
Orphanet Journal of Rare Diseases 15 (1), 1-12, 2020
Bank of Digital Filters for Identification of Combined Drug Products in a French Public Database.
A Ugon, M Courtine, K Sedki, P Quentin, M Valette, R Tsopra
Studies in health technology and informatics 270, 63-67, 2020
Laboratoire sur puce pour la détection d'événements cellulaires rares
M Valette
Université Toulouse 3 Paul Sabatier (UT3 Paul Sabatier), 2019
On-Chip Pre-Treatment of Biological Samples for the Isolation of Adipose Stem Cells (ASCs)
M Valette, M Bouguelmouna, M Mariotte, R Courson, MC Blatché, ...
2019 20th International Conference on Solid-State Sensors, Actuators and …, 2019
Adipose Stem Cells (ASCs) isolation by on-chip pre-treatment of biological samples
M Valette, M Bouguelmouna, M Mariotte, R Courson, MC Blatché, ...
Mutations du récepteur aux mélanocortines de type 4: Associations avec la perte de poids et le comportement alimentaire des sujets obèses adultes
M Valette
Paris 13, 2013
Overview of leading causes of death among French patients with Prader-Willi Syndrome, 2004-2014
DLP Alfaro, P Lemoine, V EHLINGER, C MOLINAS, G DIENE, ...
Horm Res 69 (1), 45-52, 2008
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