Encephaloduroateriosynangiosis (EDAS) in the management of Moyamoya syndrome in sickle cell disease
Autor: | Alamri, A, Hever, P, Cheserem, J, Gradil, C, Bassi, S, Tolias, CM |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2017 |
Předmět: | |
Zdroj: | 68. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), 7. Joint Meeting mit der Society of British Neurological Surgeons (SBNS); 20170514-20170517; Magdeburg; DOCMO.05.03 /20170609/ |
DOI: | 10.3205/17dgnc026 |
Popis: | Objectives: Encephalo-duro-arterio-synangiosis (EDAS) for treatment of Moyamoya syndrome (MMS) has been well described in the literature, however in MMS caused by sickle cell anaemia (SCA), EDAS use remains controversial with poor long-term follow-up. We present a case-series of such SCA patients who[for full text, please go to the a.m. URL] 68. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC), 7. Joint Meeting mit der Society of British Neurological Surgeons (SBNS) |
Databáze: | OpenAIRE |
Externí odkaz: |