Results 31 to 40 of about 15,917 (214)
Moyamoya in Hispanics: not only in Japanese
Neurology International, 2014 Moyamoya disease was first described in 1957 as hypoplasia of the bilateral internal carotid arteries, the characteristic appearance of the associated network of abnormally dilated collateral vessels on angiography was later likened to something hazy ...
Sarmad Said +5 more
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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
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BMC Neurology, 2017 Background Enlarged perivascular spaces (EPVS) are often observed with magnetic resonance imaging in patients with small vessel disease. However, the risk factors, radiological features, and clinical relevance of EPVS in patients with moyamoya disease ...
Tomoyoshi Kuribara +6 more
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The role of VEGF and KDR polymorphisms in moyamoya disease and collateral revascularization. [PDF]
PLoS ONE, 2012 We conducted a case-control study to investigate whether vascular endothelial growth factor (VEGF -2578, -1154, -634, and 936) and kinase insert domain containing receptor (KDR -604, 1192, and 1719) polymorphisms are associated with moyamoya disease ...
Young Seok Park +12 more
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Anaesthesia and Moyamoya Disease [PDF]
Anaesthesia and Intensive Care, 1995 link_to_subscribed_fulltext
Henderson, MA, Irwin, MG
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Application of DTI and fMRI in moyamoya disease
Frontiers in Neurology, 2022 Moyamoya disease (MMD) is a chronic and progressive cerebrovascular stenosis or occlusive disease that occurs near Willis blood vessels. Diffusion tensor imaging (DTI) and functional magnetic resonance imaging (fMRI) are used to detect the microstructure
Xiaokuan Hao +9 more
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Doença de Moyamoya: relato de três pacientes brasileiros [PDF]
, 1999 Moyamoya disease (MMD) is a chronic occlusive cerebrovascular disease of unknown etiology reported mainly in the Japanese. Most cases occur in children. The disease is rare in non-Oriental adults manifesting itself mostly as intracerebral hemorrhages. We
Franco, Clélia Maria Ribeiro +3 more
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Síndrome de moyamoya associada a neurofibromatose tipo I em paciente pediátrico [PDF]
, 2011 CONTEXT: Neurofibromatosis type 1 (NF-1) is the most prevalent autosomal dominant genetic disorder among humans. Moyamoya disease is a cerebral vasculopathy that is only rarely observed in association with NF-1, particularly in the pediatric age range ...
DARRIGO JÚNIOR, Luiz Guilherme +5 more
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Neurologia Medico-ChirurgicaRecent cohort studies on hemorrhagic and asymptomatic moyamoya disease have revealed that choroidal anastomosis, a type of fragile periventricular collateral pathway (periventricular anastomosis) typical of the disease, is an independent predictor of ...
Takeshi FUNAKI +2 more
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Clinical and Imaging Characteristics of Arteriopathy Subtypes in Children with Arterial Ischemic Stroke: Results of the VIPS Study. [PDF]
, 2017 Background and purposeChildhood arteriopathies are rare but heterogenous, and difficult to diagnose and classify, especially by nonexperts. We quantified clinical and imaging characteristics associated with childhood arteriopathy subtypes to facilitate ...
Barkovich, AJ +12 more
core +2 more sources