Recommendations for the Management of Strokelike Episodes in Patients With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Strokelike Episodes.

Koenig, Mary Kay; Emrick, Lisa; Karaa, Amel; Korson, Mark; Scaglia, Fernando; Parikh, Sumit; Goldstein, Amy

Koenig, Mary Kay; Emrick, Lisa; Karaa, Amel; Korson, Mark; Scaglia, Fernando; Parikh, Sumit; Goldstein, Amy.

Afiliação

Koenig MK; Departments of Pediatrics and Neurology, The University of Texas Medical School at Houston, Houston.
Emrick L; Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston.
Karaa A; Department of Genetics and Metabolism, Massachusetts General Hospital, Harvard Medical School, Boston.
Korson M; Genetic Metabolic Center for Education, Salem, Massachusetts.
Scaglia F; Department of Molecular and Human Genetics, Baylor College of Medicine and Texas Children's Hospital, Houston.
Parikh S; Center for Pediatric Neurology, Neurosciences Institute, Cleveland Clinic, Cleveland, Ohio.
Goldstein A; Department of Pediatrics, Children's Hospital of Pittsburgh of University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania.

JAMA Neurol ; 73(5): 591-4, 2016 May 01.

Article em En | MEDLINE | ID: mdl-26954033

Assuntos

Gerenciamento Clínico; Síndrome MELAS/diagnóstico; Síndrome MELAS/terapia; Humanos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome MELAS / Gerenciamento Clínico Tipo de estudo: Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: JAMA Neurol Ano de publicação: 2016 Tipo de documento: Article País de publicação: Estados Unidos

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