Results 241 to 250 of about 21,247 (273)
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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
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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
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Choreoathetosis in Moyamoya Disease
World Neurosurgery, 2021Moyamoya disease is a cerebral angiopathy characterized by bilateral progressive narrowing of internal carotid arteries, developing collateral vessels with the aspect of a "puff of smoke." The presentation with movement disorders is extremely rare. We present the case of an 11-year-old girl with low academic performance who complained of involuntary ...
Zeferino Demartini +2 more
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Clinical Neurology and Neurosurgery, 2013
Moyamoya disease (MMD) is a unique occlusive disease of the bilateral internal carotid arteries in which, compensation for occlusion results in an enrichment of collateral arteries at the base of the brain. However, the epidemiology of unilateral MMD (typical angiographic evidence of MMD unilaterally with equivocal contralateral findings), and quasi ...
Nobutaka Horie +3 more
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Moyamoya disease (MMD) is a unique occlusive disease of the bilateral internal carotid arteries in which, compensation for occlusion results in an enrichment of collateral arteries at the base of the brain. However, the epidemiology of unilateral MMD (typical angiographic evidence of MMD unilaterally with equivocal contralateral findings), and quasi ...
Nobutaka Horie +3 more
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Is “unilateral” moyamoya disease different from moyamoya disease?
Journal of Neurosurgery, 1996✓ Whether a diagnosis of moyamoya disease is justified in patients with typical angiographic evidence of moyamoya disease unilaterally and normal angiographic findings contralaterally remains controversial. In this study the authors analyzed longitudinal angiographic change, familial occurrence, and basic fibroblast growth factor (bFGF) concentration ...
Kiyohiro Houkin +3 more
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Pediatrics International, 1994
AbstractMoyamoya disease is a progressive disease which involves the internal carotid arteries and its branches bilaterally. The disease is reported both in adults and in children. Moyamoya disease is frequently seen in Japanese patients having certain human leucocyte antigen (HLA) haplotypes including HLA‐Aw24, Bw46 and Bw54.
SARENUR T. +6 more
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AbstractMoyamoya disease is a progressive disease which involves the internal carotid arteries and its branches bilaterally. The disease is reported both in adults and in children. Moyamoya disease is frequently seen in Japanese patients having certain human leucocyte antigen (HLA) haplotypes including HLA‐Aw24, Bw46 and Bw54.
SARENUR T. +6 more
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Child's Nervous System, 2010
Moyamoya disease, a rare cause of pediatric stroke, is a cerebrovascular occlusive disorder resulting from progressive stenosis of the distal intracranial carotid arteries and their proximal branches. In response to brain ischemia, there is the development of basal collateral vessels, which give rise to the characteristic angiographic appearance of ...
Edward S. Ahn +2 more
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Moyamoya disease, a rare cause of pediatric stroke, is a cerebrovascular occlusive disorder resulting from progressive stenosis of the distal intracranial carotid arteries and their proximal branches. In response to brain ischemia, there is the development of basal collateral vessels, which give rise to the characteristic angiographic appearance of ...
Edward S. Ahn +2 more
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Acta Neurologica Scandinavica, 1997
Moyamoya disease was first believed to be confined to Japan, but over the years it has been reported all over the world. We report seven cases from the University Hospital of the Faculty of Medicine of Ribeirão Preto, University of São Paulo with a review of the previously described cases in Brazil.The diagnosis was based on the diagnostic criteria of ...
Cesar Minelli +6 more
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Moyamoya disease was first believed to be confined to Japan, but over the years it has been reported all over the world. We report seven cases from the University Hospital of the Faculty of Medicine of Ribeirão Preto, University of São Paulo with a review of the previously described cases in Brazil.The diagnosis was based on the diagnostic criteria of ...
Cesar Minelli +6 more
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Moyamoya disease and anesthesia
Pediatric Anesthesia, 2005SummaryMoyamoya disease is a condition that results from bilateral stenosis or obstruction of the intracranial arteries at the base of the brain. Patients exhibit ischemic symptoms, and vascular reconstruction is the therapy of choice. Surgical treatment for Moyamoya disease is often complicated by cerebral ischemia, so the goal in perioperative ...
Adnan Dagcinar +4 more
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Cerebrovascular Moyamoya disease
European Journal of Pediatrics, 1984Clinical features of ten Japanese children with cerebrovascular Moyamoya disease are reported and non-Japanese paediatric cases of the disease are reviewed from the world literature. The most common initial manifestations were headache in four cases (40%), motor deficit and convulsion in three cases (30%).
H. Takahashi +2 more
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