Work

A hereditary moyamoya syndrome with multisystemic manifestations

Year: 2010

Type: article

Study design: Case Report

Source: Neurology

DOI: 10.1212/wnl.0b013e3181e8ee3f

Authors: D. Hervé, P. Touraine, A. Verloes, S. Miskinyte, V. Krivosic, D. Logeart, N. Alili, J.D. Laredo, A. Gaudric, E. Houdart, J.P. Metzger, E. Tournier-Lasserve, F. Woimant

Institutions: Inserm, Assistance Publique – Hôpitaux de Paris, Hôpital Fernand-Widal, Hôpital Lariboisière, Hôpital Robert-Debré

Language: English

Topic: Moyamoya disease diagnosis and treatment

Subfield: Clinical Neurology

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: Boston Scientific Corporation, Servier, Allergan, Cordis

OpenAlex ID: W2133539005

FWCI: 2.108

Cites: 23

Cited by: 47

Related to: 10