MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, Stroke) - a Diagnosis Not to be Missed.

Quinn, N M; Stone, G; Brett, F; Caro-Dominguez, P; Neylon, O; Lynch, B

Quinn, N M; Stone, G; Brett, F; Caro-Dominguez, P; Neylon, O; Lynch, B.

Afiliación

Quinn NM; Departments of Paediatrics, Neurology and Radiology, Childrens University Hospital, Temple St, Dublin 1.
Stone G; Departments of Paediatrics, Neurology and Radiology, Childrens University Hospital, Temple St, Dublin 1.
Brett F; Departments of Paediatrics, Neurology and Radiology, Childrens University Hospital, Temple St, Dublin 1.
Caro-Dominguez P; Departments of Paediatrics, Neurology and Radiology, Childrens University Hospital, Temple St, Dublin 1.
Neylon O; Departments of Paediatrics, Neurology and Radiology, Childrens University Hospital, Temple St, Dublin 1.
Lynch B; Departments of Paediatrics, Neurology and Radiology, Childrens University Hospital, Temple St, Dublin 1.

Ir Med J ; 109(8): 455, 2016 Sep 09.

Article en En | MEDLINE | ID: mdl-28124854

Asunto(s)

Síndrome MELAS/diagnóstico; Diagnóstico Tardío; Diagnóstico Diferencial; Epilepsia/complicaciones; Humanos; Recién Nacido; Recien Nacido Prematuro; Masculino

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Banco de datos: MEDLINE Asunto principal: Síndrome MELAS Tipo de estudio: Diagnostic_studies Límite: Humans / Male / Newborn Idioma: En Revista: Ir Med J Año: 2016 Tipo del documento: Article

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