Results 181 to 190 of about 12,785 (220)
Some of the next articles are maybe not open access.
Child's Nervous System, 1988
The authors reviewed the Japanese literature on moyamoya disease. In the article we discuss the history of such investigations in Japan, the signs and symptoms, the diagnosis (especially concerning diagnostic criteria and magnetic resonance imaging), the pathology in relation to its etiology, and the current methods of treatment. On the whole, the main
Y, Maki, T, Enomoto
openaire +2 more sources
The authors reviewed the Japanese literature on moyamoya disease. In the article we discuss the history of such investigations in Japan, the signs and symptoms, the diagnosis (especially concerning diagnostic criteria and magnetic resonance imaging), the pathology in relation to its etiology, and the current methods of treatment. On the whole, the main
Y, Maki, T, Enomoto
openaire +2 more sources
Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova, 2014
Moyamoya syndrome is a rare chronic progressive disease of brain vessels in which certain arteries in the brain are constricted. During the disease a collateral circulation develops around the blocked vessels to compensate for the blockage, and on angiography these collateral vessels have the appearance of a "puff of smoke".
K I, Burkova +7 more
openaire +2 more sources
Moyamoya syndrome is a rare chronic progressive disease of brain vessels in which certain arteries in the brain are constricted. During the disease a collateral circulation develops around the blocked vessels to compensate for the blockage, and on angiography these collateral vessels have the appearance of a "puff of smoke".
K I, Burkova +7 more
openaire +2 more sources
Moyamoya-like vasculopathy (moyamoya syndrome) in children
Child's Nervous System, 2004A large variety of inherited or acquired childhood disorders and conditions may present in conjunction with progressive bilateral stenosis and/or occlusion of the terminal segments of the internal carotid artery. In addition, the development of pathological collateral vessels can be observed in the vicinity of the steno-occlusive changes in these ...
Peter, Horn +4 more
openaire +2 more sources
Moyamoya Disease (Moyamoya Syndrome) and Coarctation of the Aorta
Neuropediatrics, 2000info:eu-repo/semantics ...
Christiaens, Florence +3 more
openaire +2 more sources
Current Treatment Options in Neurology, 2012
The arteriopathy of moyamoya is progressive and results in severe disability from cerebral ischemia. Once the diagnosis is confirmed with magnetic resonance imaging (MRI) and catheter angiography, initial measures should consist of administration of low dose aspirin (usually 81 mg daily, barring pre-existing contraindications), maintenance of good ...
openaire +2 more sources
The arteriopathy of moyamoya is progressive and results in severe disability from cerebral ischemia. Once the diagnosis is confirmed with magnetic resonance imaging (MRI) and catheter angiography, initial measures should consist of administration of low dose aspirin (usually 81 mg daily, barring pre-existing contraindications), maintenance of good ...
openaire +2 more sources
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 ...
Kentaro, Hayashi +3 more
openaire +2 more sources
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 ...
Kentaro, Hayashi +3 more
openaire +2 more sources
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 ...
K, Houkin +3 more
openaire +2 more sources
Comparison between moyamoya disease and moyamoya syndrome in Israel
Journal of Stroke and Cerebrovascular DiseasesMoyamoya is a chronic brain vasculopathy involving the distal intracranial internal carotid artery (ICA) or proximal middle cerebral artery (MCA). Moyamoya patients can be divided into those with primary moyamoya disease (MMD) and those with moyamoya secondary to other known causes such as intracranial atherosclerosis (moymoya syndrome [MMS]).
Y. Schwartzmann +8 more
openaire +2 more sources
Clinical Management of Moyamoya Patients
Journal of Clinical Medicine, 2021Laura Gatti +2 more
exaly

