Familial occurrence of moya-moya disease: report of three Japanese families

Author:

Kitahara T.,Ariga N.,Yamaura A.,Makino H.,Maki Y.

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference26 articles.

1. Bilateral temporal middle cerebral artery anastomosis for moyamoya syndrome;Amine, A.R.C.; Moody, R.A.; Meeks, W.;Surgical Neurology,1977

2. Idiopathic occlusive arterial disorders in the cervical region and the main trunks of the cerebral arteries in Japan. A disease with abnormal intracranial vascular networks-spontaneous occlusion of the circle of Willis. Igaku Shoin Tokyo;Handa, H.; Tani, E.; Handa, J.; Kondo, A.; Kikuchi, H.; Sato, K.,1967

3. Occurrence of moyamoya disease in father and daughter;Hashimoto, T.; Sato, J.; Sakai, H.; Nakamura, N.,1978

4. Operative revascularization des zirkulatorisch geschadigten Gehirns durch Anlegen gestielter Muskellappen;Henschen, C.;Chirurgie; Beitrage fiur Klinische,1950

5. A surgical treatment of "Moyamoya" disease. Encephalo-myo synangiosis;Karasawa, J.; Kikuchi, H.; Furuse, S.; Sakaki, T.; Yoshida, Y.; Ohnishi, H.; Taki, W.;Neurologia medicochirurgica,1977

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