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Causes of death in Prader-Willi syndrome: lessons from 11 years' experience of a national reference center.
Pacoricona Alfaro, Dibia Liz; Lemoine, Perrine; Ehlinger, Virginie; Molinas, Catherine; Diene, Gwénaëlle; Valette, Marion; Pinto, Graziella; Coupaye, Muriel; Poitou-Bernert, Christine; Thuilleaux, Denise; Arnaud, Catherine; Tauber, Maithé.
Afiliación
  • Pacoricona Alfaro DL; UMR 1027 Inserm- Paul Sabatier University, Toulouse, France.
  • Lemoine P; Endocrinology, Obesity, Bone Diseases, Genetics and Gynecology Unit, Children's Hospital, University Hospital Center of Toulouse, Toulouse, France.
  • Ehlinger V; UMR 1027 Inserm- Paul Sabatier University, Toulouse, France.
  • Molinas C; Endocrinology, Obesity, Bone Diseases, Genetics and Gynecology Unit, Children's Hospital, University Hospital Center of Toulouse, Toulouse, France.
  • Diene G; French National Reference Center for Prader-Willi Syndrome, Children's Hospital, University Hospital Center of Toulouse, 330, avenue de Grande-Bretagne - TSA 40031, 31059, Toulouse cedex 9, France.
  • Valette M; Centre de Physiopathologie de Toulouse-Purpan, UMR 5282 CNRS, UMR 1043 Inserm, Paul Sabatier University, Toulouse, France.
  • Pinto G; UMR 1027 Inserm- Paul Sabatier University, Toulouse, France.
  • Coupaye M; Endocrinology, Obesity, Bone Diseases, Genetics and Gynecology Unit, Children's Hospital, University Hospital Center of Toulouse, Toulouse, France.
  • Poitou-Bernert C; French National Reference Center for Prader-Willi Syndrome, Children's Hospital, University Hospital Center of Toulouse, 330, avenue de Grande-Bretagne - TSA 40031, 31059, Toulouse cedex 9, France.
  • Thuilleaux D; Endocrinology, Obesity, Bone Diseases, Genetics and Gynecology Unit, Children's Hospital, University Hospital Center of Toulouse, Toulouse, France.
  • Arnaud C; French National Reference Center for Prader-Willi Syndrome, Children's Hospital, University Hospital Center of Toulouse, 330, avenue de Grande-Bretagne - TSA 40031, 31059, Toulouse cedex 9, France.
  • Tauber M; Pediatric Endocrinology, Diabetology and Gynecology Department, Assistance-Publique Hôpitaux de Paris (AP-HP), Necker Children's University Hospital, Paris, France.
Orphanet J Rare Dis ; 14(1): 238, 2019 11 04.
Article en En | MEDLINE | ID: mdl-31684997
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi Tipo de estudio: Etiology_studies / Observational_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Francia
Texto completo
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PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Síndrome de Prader-Willi Tipo de estudio: Etiology_studies / Observational_studies Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2019 Tipo del documento: Article País de afiliación: Francia