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Type 0 Spinal Muscular Atrophy: Further Delineation of Prenatal and Postnatal Features in 16 Patients.
Grotto, Sarah; Cuisset, Jean-Marie; Marret, Stéphane; Drunat, Séverine; Faure, Patricia; Audebert-Bellanger, Séverine; Desguerre, Isabelle; Flurin, Vincent; Grebille, Anne-Gaëlle; Guerrot, Anne-Marie; Journel, Hubert; Morin, Gilles; Plessis, Ghislaine; Renolleau, Sylvain; Roume, Joëlle; Simon-Bouy, Brigitte; Touraine, Renaud; Willems, Marjolaine; Frébourg, Thierry; Verspyck, Eric; Saugier-Veber, Pascale.
Afiliación
  • Grotto S; Department of Genetics, Normandy Center for Medical Genomics and Personalized Medicine, Rouen University Hospital, Rouen, France.
  • Cuisset JM; Department of Pediatric Neurology, Roger Salengro Hospital, Lille Regional University Hospital, Lille, France.
  • Marret S; Department of Pediatric Intensive Care, Rouen University Hospital, Rouen, France.
  • Drunat S; Inserm ERI 28, Institute for Research and Innovation in Biomedicine, Rouen University, France.
  • Faure P; Department of Genetics, Robert Debre University Hospital, APHP, Paris, France.
  • Audebert-Bellanger S; Inserm U1079, Institute for Research and Innovation in Biomedicine, Rouen University, Rouen, France.
  • Desguerre I; Department of Pediatrics and Genetics, Brest Regional University Hospital, Brest, France.
  • Flurin V; Department of Pediatric Neurology, Necker-Enfants Malades Hospital, APHP, Paris, France.
  • Grebille AG; Department of Pediatric Intensive Care, Le Mans Hospital, Le Mans, France.
  • Guerrot AM; Department of Obstetrics and Gynecology, Saint-Brieuc Hospital, Saint-Brieuc, France.
  • Journel H; Department of Genetics, Normandy Center for Medical Genomics and Personalized Medicine, Rouen University Hospital, Rouen, France.
  • Morin G; Department of Genetics, Vannes Bretagne-Atlantique Hospital, Vannes, France.
  • Plessis G; Department of Genetics, Amiens University Hospital, Amiens, France.
  • Renolleau S; Department of Genetics, Caen University Hospital, Caen, France.
  • Roume J; Department of Pediatric Intensive Care, Armand-Trousseau Children's Hospital, APHP, Paris, France.
  • Simon-Bouy B; Department of Genetics, Poissy-Saint-Germain-en-Laye Hospital, Poissy, France.
  • Touraine R; Department of Genetics, Versailles Hospital, Le Chesnay, France.
  • Willems M; Department of Genetics, Saint-Etienne University Hospital, Saint-Priest-en-Jarez, France.
  • Frébourg T; Department of Genetics, Necker-Enfants Malades Hospital, APHP, Paris, France.
  • Verspyck E; Department of Genetics, Normandy Center for Medical Genomics and Personalized Medicine, Rouen University Hospital, Rouen, France.
  • Saugier-Veber P; Inserm U1079, Institute for Research and Innovation in Biomedicine, Rouen University, Rouen, France.
J Neuromuscul Dis ; 3(4): 487-495, 2016 11 29.
Article en En | MEDLINE | ID: mdl-27911332
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Artrogriposis / Síndrome de Dificultad Respiratoria del Recién Nacido / Enfermedades del Sistema Nervioso Autónomo / Atrofias Musculares Espinales de la Infancia / Enfermedades de los Nervios Craneales / Cardiopatías Congénitas / Hipotonía Muscular Tipo de estudio: Diagnostic_studies / Etiology_studies Aspecto: Patient_preference Límite: Female / Humans / Male / Newborn Idioma: En Revista: J Neuromuscul Dis Año: 2016 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Países Bajos
Buscar en Google
Añadir a Mi BVS
Imprimir
XML
PubMed Links

Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Artrogriposis / Síndrome de Dificultad Respiratoria del Recién Nacido / Enfermedades del Sistema Nervioso Autónomo / Atrofias Musculares Espinales de la Infancia / Enfermedades de los Nervios Craneales / Cardiopatías Congénitas / Hipotonía Muscular Tipo de estudio: Diagnostic_studies / Etiology_studies Aspecto: Patient_preference Límite: Female / Humans / Male / Newborn Idioma: En Revista: J Neuromuscul Dis Año: 2016 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Países Bajos