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Sleep-disordered breathing and its management in children with rare skeletal dysplasias.
Nguyen, Duy Bo; Khirani, Sonia; Griffon, Lucie; Baujat, Geneviève; Michot, Caroline; Marzin, Pauline; Rondeau, Sophie; Luscan, Romain; Couloigner, Vincent; Pejin, Zagorka; Zerah, Michel; Cormier-Daire, Valérie; Fauroux, Brigitte.
Afiliación
  • Nguyen DB; AP-HP, Hôpital Necker-Enfants Malades, Pediatric Noninvasive Ventilation and Sleep Unit, Paris, France.
  • Khirani S; Pediatric Department, Vinmec Times City Hospital, Hanoi, Vietnam.
  • Griffon L; AP-HP, Hôpital Necker-Enfants Malades, Pediatric Noninvasive Ventilation and Sleep Unit, Paris, France.
  • Baujat G; EA 7330 VIFASOM (Vigilance Fatigue Sommeil et Santé Publique), Paris University, Paris, France.
  • Michot C; ASV Santé, Gennevilliers, France.
  • Marzin P; AP-HP, Hôpital Necker-Enfants Malades, Pediatric Noninvasive Ventilation and Sleep Unit, Paris, France.
  • Rondeau S; EA 7330 VIFASOM (Vigilance Fatigue Sommeil et Santé Publique), Paris University, Paris, France.
  • Luscan R; AP-HP, Hôpital Necker-Enfants Malades, Genetics Department, National Reference Centre for Skeletal Dysplasia, Paris University, INSERM UMR 1163, Institut Imagine, Paris, France.
  • Couloigner V; AP-HP, Hôpital Necker-Enfants Malades, Genetics Department, National Reference Centre for Skeletal Dysplasia, Paris University, INSERM UMR 1163, Institut Imagine, Paris, France.
  • Pejin Z; AP-HP, Hôpital Necker-Enfants Malades, Genetics Department, National Reference Centre for Skeletal Dysplasia, Paris University, INSERM UMR 1163, Institut Imagine, Paris, France.
  • Zerah M; AP-HP, Hôpital Necker-Enfants Malades, Genetics Department, National Reference Centre for Skeletal Dysplasia, Paris University, INSERM UMR 1163, Institut Imagine, Paris, France.
  • Cormier-Daire V; AP-HP, Hôpital Necker-Enfants malades, Pediatric Otolaryngology Department, National Reference Centre for ENT Rare Malformations, Paris, France.
  • Fauroux B; AP-HP, Hôpital Necker-Enfants malades, Pediatric Otolaryngology Department, National Reference Centre for ENT Rare Malformations, Paris, France.
Am J Med Genet A ; 185(7): 2108-2118, 2021 07.
Article en En | MEDLINE | ID: mdl-33908178
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteocondrodisplasias / Costillas / Síndromes de la Apnea del Sueño / Columna Vertebral / Apnea Obstructiva del Sueño / Disostosis / Discapacidad Intelectual Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteocondrodisplasias / Costillas / Síndromes de la Apnea del Sueño / Columna Vertebral / Apnea Obstructiva del Sueño / Disostosis / Discapacidad Intelectual Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Estados Unidos