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Vessel wall imaging in adult moyamoya disease with presumed acute in situ thrombotic occlusion: illustrative cases. [PDF]
J Neurosurg Case LessonsFunaki T +8 more
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Moyamoya Disease and Moyamoya Syndrome
New England Journal of Medicine, 2009Moyamoya disease is a cerebrovascular condition predisposing affected patients to stroke in association with progressive stenosis of the intracranial internal carotid arteries and their proximal branches. Patients with characteristic moyamoya vasculopathy plus associated conditions are categorized as having moyamoya syndrome.
R Michael, Scott, Edward R, Smith
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Stroke, 1996 Background and Purpose Moyamoya disease is a chronic occlusive cerebrovascular disorder characterized by progressive stenosis of the supraclinoid internal carotid artery, with the secondary development of enlarged basal ...
Richard Robertson +2 more
exaly +2 more sources
Ugeskrift for laeger, 2011
The disease moyamoya is rare in Europe, but it is seen more frequently in Japan and other Asian countries. Moyamoya is characterized by progressing occlusion of the cerebral arteries and secondary development of pathological collateral vessels induced by ischaemia.
Hansen, Rikke Nymark +2 more
openaire +4 more sources
The disease moyamoya is rare in Europe, but it is seen more frequently in Japan and other Asian countries. Moyamoya is characterized by progressing occlusion of the cerebral arteries and secondary development of pathological collateral vessels induced by ischaemia.
Hansen, Rikke Nymark +2 more
openaire +4 more sources
Angiogenic Factors in Moyamoya Disease
Stroke, 1996 Background and Purpose We previously reported that the level of basic fibroblast growth factor (bFGF) is high in cerebrospinal fluid (CSF) taken from patients with moyamoya disease.
Kiyohiro Houkin +2 more
exaly +2 more sources
World Neurosurgery, 2017
More than 50 years have elapsed since moyamoya disease was initially described; however, the disease etiology remains unknown. Although certain genetic loci and immunologic characteristics are associated with moyamoya disease, this does not fully explain its pathophysiology.
Juan C, Mejia-Munne +4 more
openaire +2 more sources
More than 50 years have elapsed since moyamoya disease was initially described; however, the disease etiology remains unknown. Although certain genetic loci and immunologic characteristics are associated with moyamoya disease, this does not fully explain its pathophysiology.
Juan C, Mejia-Munne +4 more
openaire +2 more sources
Journal of Neurosurgery: Pediatrics, 2007
Abstract: Object. The authors' aim in this Study was to review their experience in the use of indirect revascularization alone in a series of 14 children with moyamoya disease, in which numerous bur holes and arachnoid openings were made over each affected hemisphere. Methods.
Menovsky, Tomas, De Ridder, Dirk
openaire +2 more sources
Abstract: Object. The authors' aim in this Study was to review their experience in the use of indirect revascularization alone in a series of 14 children with moyamoya disease, in which numerous bur holes and arachnoid openings were made over each affected hemisphere. Methods.
Menovsky, Tomas, De Ridder, Dirk
openaire +2 more sources