Cerebral arteriopathy in ACTA2 mutations: a spectrum of disease highlighted by a case of variable penetrance in two siblings. | J Neurosurg Pediatr;27(4): 446-451, 2021 Jan 29. | MEDLINE

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Cerebral arteriopathy in ACTA2 mutations: a spectrum of disease highlighted by a case of variable penetrance in two siblings.

Tschoe, Christine; Kim, Teddy E; Fargen, Kyle M; Wolfe, Stacey Q.

J Neurosurg Pediatr ; 27(4): 446-451, 2021 Jan 29.

Article in En | MEDLINE | ID: mdl-33513575

Subject(s)
Key words

ACTA2 mutation; Arg258 substitution; cerebral arteriopathy; indirect revascularization; moyamoya disease; pial encephalodural synangiosis; vascular disorders

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebral Arterial Diseases / Actins Limits: Adolescent / Child / Humans / Male Language: En Journal: J Neurosurg Pediatr Journal subject: NEUROCIRURGIA / PEDIATRIA Year: 2021 Document type: Article Country of publication: Estados Unidos

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebral Arterial Diseases / Actins Limits: Adolescent / Child / Humans / Male Language: En Journal: J Neurosurg Pediatr Journal subject: NEUROCIRURGIA / PEDIATRIA Year: 2021 Document type: Article Country of publication: Estados Unidos