Results 31 to 40 of about 21,247 (273)
Experimental study of the pathogenesis of moyamoya disease: histological changes in the arterial wall caused by immunological reactions in monkeys. [PDF]
, 2003 Moyamoya disease is a progressive vascular disorder of unknown etiology. Theories of inflammatory and immunologic mechanisms have been proposed as the pathogeneses.
Kamata, Ichiro +2 more
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Moyamoya: A Review of the Disease and Current Treatments [PDF]
, 2014 INTRODUCTION Moyamoya disease is a rare progressive cerebrovascular disease characterized by bilateral stenosis of vasculature of the Circle of Willis, specifically the distal internal carotid arteries, that leads to extensive collateral circulation ...
Anderson, Eliza +6 more
core +2 more sources
RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients. [PDF]
PLoS ONE, 2016 RNF213/Mysterin has been identified as a susceptibility gene for moyamoya disease, a cerebrovascular disease characterized by occlusive lesions in the circle of Willis.
Hatasu Kobayashi +19 more
doaj +1 more source
Unilateral moyamoya disease with co-existing arteriovenous malformation [PDF]
, 2006 A case of an intracerebral bleed in a young man with a rare combination of arteriovenous malformation (AVM) and unilateral moyamoya disease is presented.
Mohd Ramli, Norlisah +2 more
core +1 more source
The Genetic Basis of Moyamoya Disease [PDF]
Translational Stroke Research, 2021 AbstractMoyamoya disease (MMD) is a rare cerebrovascular disease characterized by progressive spontaneous bilateral occlusion of the intracranial internal cerebral arteries (ICA) and their major branches with compensatory capillary collaterals resembling a “puff of smoke” (Japanese: Moyamoya) on cerebral angiography.
Martin A. Mensah +9 more
openaire +6 more sources
Subarachnoid Hemorrhage from Posterior Cerebral Artery Aneurysm during Puerperium – Case Report and Review of Literature [PDF]
, 2012 Subarachnoid hemorrhages (SAH) due to true aneurysms of the Posterior Cerebral Artery (PCA) during puerperium in young and healthy females are extremely rare.
Brawanski, Alexander +4 more
core +1 more source
Moyamoya Syndrome: A Window of Moyamoya Disease [PDF]
Journal of Korean Neurosurgical Society, 2015 Moyamoya-like vasculopathy develops in association with various systemic diseases and conditions, which is termed moyamoya syndrome. Relatively common diseases and conditions are related to moyamoya syndrome, including neurofibromatosis type 1, Down syndrome, thyroid disease, and cranial irradiation.
Seung-Ki Kim +3 more
openaire +2 more sources
Frontiers in Neurology, 2021 Moyamoya disease is an idiopathic chronically progressive cerebrovascular disease, which causes both ischemic and hemorrhagic stroke. Genetic studies identified RNF213/Mysterin and GUCY1A3 as disease-causing genes.
Yohei Mineharu, Susumu Miyamoto
doaj +1 more source
Neural Regeneration Research, 2021 Although intracranial hemorrhage in moyamoya disease can occur repeatedly, predicting the disease is difficult. Deep learning algorithms developed in recent years provide a new angle for identifying hidden risk factors, evaluating the weight of different
Yu Lei +9 more
doaj +1 more source
Aneurysms of the intracranial segment of the ophthalmic artery trunk. case report and systematic literature review [PDF]
, 2017 Aneurysms arising from the ophthalmic artery trunk (OAT) are very rare, particularly in the artery's intracranial course. The onset of a subarachnoid hemorrhage (SAH) from a ruptured OAT aneurysm in this segment is extremely rare.
C. Colonnese +5 more
core +1 more source