Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Kuzma Strenilkov"'
Autor:
Kuzma Strenilkov, Jimmy Debladis, Juliette Salles, Marion Valette, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone, Maïthé Tauber
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Abstract Background Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, i
Externí odkaz:
https://doaj.org/article/1f3b3d235f8d4386a0fa41da577da8a7
Autor:
Jimmy Debladis, Marion Valette, Kuzma Strenilkov, Carine Mantoulan, Denise Thuilleaux, Virginie Laurier, Catherine Molinas, Pascal Barone, Maïthé Tauber
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-13 (2019)
Abstract Background Faces are critical social cues that must be perfectly processed in order to engage appropriately in everyday social interactions. In Prader-Willi Syndrome (PWS), a rare genetic disorder characterized by cognitive and behavioural d
Externí odkaz:
https://doaj.org/article/120d85666e6c44a9aeff658126efa733
Autor:
Marion Valette, Maithé Tauber, Carine Mantoulan, Kuzma Strenilkov, Pascal Barone, Denise Thuilleaux, Juliette Salles, Virginie Laurier, Catherine Molinas, Jimmy Debladis
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15, ⟨10.1186/s13023-020-1298-8⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15 (1), ⟨10.1186/s13023-020-1298-8⟩
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15, ⟨10.1186/s13023-020-1298-8⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2020, 15 (1), ⟨10.1186/s13023-020-1298-8⟩
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Background Prader-Willi syndrome (PWS) is a rare and complex neurodevelopmental disorder of genetic origin. It manifests itself in endocrine and cognitive problems, including highly pronounced hyperphagia and severe obesity. In many cases, impaired a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ba7378a79e3d8f08bf9d9f0398b7fe9
https://hal.archives-ouvertes.fr/hal-03093987
https://hal.archives-ouvertes.fr/hal-03093987