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Late moyamoya-like angiopathy syndrome revealing MAP2K1 Noonan syndrome.
Méreaux, J-L; Triquenot, A; Drunat, S; Cavé, H; Guyant-Maréchal, L; Goldenberg, A.
Afiliación
  • Méreaux JL; Neurology department, Rouen University Hospital, CHU de Rouen, 1, rue de Germont, 76000 Rouen, France. Electronic address: jeanloup.mereaux@gmail.com.
  • Triquenot A; Neurology department, Rouen University Hospital, CHU de Rouen, 1, rue de Germont, 76000 Rouen, France.
  • Drunat S; Département de génétique, hôpital Robert-Debré, 48, boulevard Sérurier, 75019 Paris, France.
  • Cavé H; Département de génétique, hôpital Robert-Debré, 48, boulevard Sérurier, 75019 Paris, France; Université de Paris, Paris, France.
  • Guyant-Maréchal L; Neurology department, Rouen University Hospital, CHU de Rouen, 1, rue de Germont, 76000 Rouen, France; Medical Genetics department, Rouen University Hospital, Rouen, France; Inserm U1245, department of Genetics and Reference Center for Developmental Disorders, FHU G4 Génomique, Normandie University,
  • Goldenberg A; Medical Genetics department, Rouen University Hospital, Rouen, France; Inserm U1245, department of Genetics and Reference Center for Developmental Disorders, FHU G4 Génomique, Normandie University, Unirouen, CHU de Rouen, 76000 Rouen, France.
Rev Neurol (Paris) ; 178(3): 263-265, 2022 03.
Article en En | MEDLINE | ID: mdl-34565623

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Moyamoya / Síndrome de Noonan Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Rev Neurol (Paris) Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad de Moyamoya / Síndrome de Noonan Tipo de estudio: Diagnostic_studies Límite: Humans Idioma: En Revista: Rev Neurol (Paris) Año: 2022 Tipo del documento: Article