نتایج جستجو برای: moyamoya disease
تعداد نتایج: 1490367 فیلتر نتایج به سال:
BACKGROUND AND PURPOSE We report the clinical features and longitudinal outcome of the largest cohort of patients with moyamoya disease described from a single institution in the western hemisphere. Moyamoya disease in Asia usually presents with ischemic stroke in children and intracranial hemorrhage in adults. METHODS Our study population included all patients with moyamoya disease evaluated...
To cite: Gold JJ, Dory CE, Levy ML, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/bcr-2013009812 DESCRIPTION A 17-year-old girl with a clinical diagnosis of neurofibromatosis type 1 (NF-1) presented for a routine follow-up with worsening headaches, leftsided hemiparesis and hyper-reflexia. Her medical history was significant for prematurity, speech delay and ...
BACKGROUND AND PURPOSE Postoperative hyperperfusion-related transient neurological deficits (TNDs) are frequently observed in adult patients with moyamoya disease who undergo direct bypass procedures. The present study evaluated the effect of the free radical scavenger edaravone on postoperative hyperperfusion in adult moyamoya disease. METHODS This study included 92 hemispheres in 72 adult p...
Background: Ankylosing spondylitis was reported to associate with an increased risk of cerebrovascular diseases. In this article, we aimed to report the first case of ankylosing spondylitis associated with moyamoya disease treated with encephalo-duroarterio-synangiosis. Case presentation: A 9-year-old boy with ankylosing spondylitis appeared a symptom of repeated transient ischemic attacks whic...
OBJECTIVES To elucidate the association between antiplatelet use in patients with non-haemorrhagic moyamoya disease before hospital admission and good functional status on admission in Japan. DESIGN Retrospective, multicentre, non-randomised, observational study. SETTING Nationwide registry data in Japan. PARTICIPANTS A total of 1925 patients with non-haemorrhagic moyamoya disease admitte...
OBJECTIVES To report a rare case of moyamoya syndrome with primary antiphospholipid syndrome (APS). CLINICAL PRESENTATION AND INTERVENTION A 41-year-old woman was admitted with sudden onset of left-sided hemiparesis. Magnetic resonance imaging and magnetic resonance angiography of the brain showed characteristic features of moyamoya vessels. Laboratory investigations revealed raised levels of...
Moyamoya disease is a cerebrovascular disorder characterized by stenosis or occlusion of the terminal portions of the internal carotid arteries which rarely coexists with Graves' disease. We recently experienced a rare case of Graves’ disease accompanied by moyamoya disease that presented as a stroke and recurrent stroke. 20-year-old female was initially admitted to our hospital because of thro...
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