Guidelines for Diagnosis and Treatment of Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis)
- 1 January 2012
- journal article
- practice guideline
- Published by Japan Neurosurgical Society in Neurologia medico-chirurgica
- Vol. 52 (5), 245-266
- https://doi.org/10.2176/nmc.52.245
Abstract
No abstract availableThis publication has 97 references indexed in Scilit:
- Combined direct anastomosis and encephaloduroarteriogaleosynangiosis using inverted superficial temporal artery–galeal flap and superficial temporal artery–galeal pedicle in adult moyamoya diseaseSurgical Neurology, 2006
- Inheritance pattern of familial moyamoya disease: autosomal dominant mode and genomic imprintingJournal of Neurology, Neurosurgery & Psychiatry, 2006
- Magnetic resonance angiography evaluation of external carotid artery tributaries in moyamoya diseaseSurgical Neurology, 2005
- Adult unilateral moyamoya disease with familial occurrence in two definite cases: a case report and review of the literatureNeurosurgical Review, 2005
- A novel susceptibility locus for moyamoya disease on chromosome 8q23Journal of Human Genetics, 2004
- A Co-Operative Study: Clinical Characteristics of 334 Korean Patients with Moyamoya Disease Treated at Neurosurgical Institutes (1976-1994)Acta Neurochirurgica, 2000
- Indirect revascularization for moyamoya disease: Is there a beneficial effect for adult patients?Surgical Neurology, 1996
- Children with unilateral occlusion or stenosis of the ICA associated with surrounding Moyamoya vessels — “unilateral” Moyamoya diseaseActa Neurochirurgica, 1994
- Cerebrovascular bypass surgery for the treatment of Moyamoya disease: Unsatisfactory outcome in the patients presenting with intracranial hemorrhageSurgical Neurology, 1993
- Prognosis of occlusive disease of the circle of Willis (moyamoya disease) in childrenPediatric Neurology, 1985