نتایج جستجو برای: moyamoya disease

تعداد نتایج: 1490367  

2003
Chang Min Lee Sang Yeob Lee Seung Hoon Ryu Sung Won Lee Kyung Won Park Won Tae Chung

We report on a 13-year-old female with systemic lupus erythematosus (SLE) who exhibited symptoms of severe migraine and familial moyamoya disease. Cerebral magnetic resonance angiography (MRA) showed stenosis and occlusion of the bilateral internal carotid arteries associated with the development of collateral circulation (moyamoya vessels). In a child, as in this case, headaches with cerebral ...

Journal: :JPMA. The Journal of the Pakistan Medical Association 2003
K B Asumal N Akhtar N A Syed S Shafqat S M Baig

OBJECTIVE AND BACKGROUND Moyamoya disease is an idiopathic vasculopathy of circle of Willis. Stroke is a common presentation. We describe clinical and radiological features of moyamoya disease in four patients. SETTING Tertiary care center in a metropolitan city. MATERIALS AND METHODS Patients with moyamoya disease were identified by ICD-9 coding system of the hospital medical records. Demo...

Journal: :Radiology 1995
I Yamada S Suzuki Y Matsushima

PURPOSE To evaluate magnetic resonance (MR) angiography and MR imaging in assessment of moyamoya disease. MATERIALS AND METHODS The cases of 26 patients with moyamoya disease were evaluated prospectively. After three-dimensional time-of-flight 1.5-T MR angiography and MR imaging, images were evaluated in blinded separate interpretation. RESULTS MR angiography and MR imaging accurately depic...

2012
Young Seok Park Young Joo Jeon Hyun Seok Kim Kyu Young Chae Seung-Hun Oh In Bo Han Hyun Sook Kim Won-Chan Kim Ok-Joon Kim Tae Gon Kim Joong-Uhn Choi Dong-Seok Kim Nam Keun Kim

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. Korean patients with moyamoya disease (n = 107, mean age, 20.9±15.9 years; 66.4% female) and 243 healthy control subjects (mean age, 23.0±16.1 yea...

2016
Julian Choi Perin Suthakar Farbod Farmand

We describe the case of a young Hispanic female who presented with thyrotoxicosis with seizures and ischemic stroke. She was diagnosed with a rare vasculopathy - moyamoya syndrome. After starting antithyroid therapy, her neurologic symptoms did not improve. Acute neurosurgical intervention had relieved her symptoms in the immediate post-operative period after re-anastomosis surgery. However, 2 ...

Journal: :Stroke 2001
I Yamada T Nakagawa Y Matsushima H Shibuya

BACKGROUND AND PURPOSE High-resolution turbo MR angiography with zero-filling interpolation (ZFI) technique is a new vascular imaging method with reduced scan time. The purpose of the present study was to evaluate high-resolution turbo MR angiography for the diagnosis and assessment of moyamoya disease. METHODS Forty-six patients suspected of having moyamoya disease were examined with high-re...

Journal: :The New England journal of medicine 2009
R Michael Scott Edward R Smith

Copyright © 2009 Massachusetts Medical Society. The moyamoya syndrome is a cerebrovascular condition that predisposes affected patients to stroke in association with progressive stenosis of the intracranial internal carotid arteries and their proximal branches. Reduced blood flow in the major vessels of the anterior circulation of the brain leads to compensatory development of collateral vascul...

Journal: :Brain & development 2011
Jun-ichi Takanashi

Moyamoya disease is an uncommon cerebrovascular disease characterized by progressive steno-occlusive changes in the terminal internal carotid arteries (ICA) and their main branches, associated with the development of moyamoya vessels. The incidence of the disease is high in east Asia, especially in Japan and Korea. The familial form accounts for 10-15%. Moyamoya disease has two age distribution...

Journal: :The Tohoku journal of experimental medicine 2015
Miki Fujimura Teiji Tominaga

Moyamoya disease is a chronic cerebrovascular disease with unknown etiology, which is characterized by bilateral steno-occlusive changes at the terminal portion of the internal carotid artery and an abnormal vascular network formation at the base of the brain. Moyamoya disease is known to have unique and dynamic nature to convert the vascular supply for the brain from internal carotid (IC) syst...

Journal: :Postgraduate Medical Journal 1997

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