Results 21 to 30 of about 5,183,178 (176)

Clinical value of the systemic immune-inflammation index in moyamoya disease

Frontiers in Neurology, 2023
BackgroundMoyamoya disease (MMD) is a rare cerebrovascular disorder with unknown etiology. The underlying pathophysiological mechanism of moyamoya disease remains to be elucidated, but recent studies have increasingly highlighted that abnormal immune ...
Erheng Liu, Erheng Liu, Chengyuan Liu, Chengyuan Liu, Lide Jin, Hu Zhou, Xueyi Tan, Xueyi Tan, Guibo Zhang, Guibo Zhang, Weihua Tao, Xiang Gao, Heng Zhao, Chao Luo, Xuehua Li, Shuaifeng Yang   +15 more
doaj   +1 more source

Research progress of moyamoya disease combined with renovascular hypertension

Frontiers in Surgery, 2022
Moyamoya disease (MMD) is an idiopathic cerebrovascular disease which was first described by Suzuki and Takaku in 1969. Moyamoya disease is a non-atherosclerotic cerebrovascular structural disorder.
Erheng Liu, Erheng Liu, Heng Zhao, Chengyuan Liu, Chengyuan Liu, Xueyi Tan, Xueyi Tan, Chao Luo, Chao Luo, Shuaifeng Yang   +9 more
doaj   +1 more source

The risk for future cerebrovascular disease in pregnant women with Moyamoya disease: a nationwide population-based study in South Korea

BMC Pregnancy and Childbirth, 2022
Background Physiologic changes during pregnancy affect the development of postpartum cerebrovascular disease (CVD) in women with Moyamoya disease. Due to the rare prevalence of Moyamoya disease and its large regional variations, large-scale based studies
Yeonseong Jeong, Yun Ji Jung, Eunjin Noh, Sungyeon Ha, Jeongeun Hwang, Geum Joon Cho, Min-Jeong Oh, Young-Han Kim   +7 more
doaj   +1 more source

Abstract Number ‐ 281: Clinical and Epidemiological Characteristics of Moyamoya Disease Presenting with Concomitant Autoimmune Conditions

Stroke: Vascular and Interventional Neurology, 2023
Introduction Moyamoya disease was first described in the 1950’s. After over six decades, however, the underlying etiology of Moyamoya still remains unknown.
Nolan Brown, Rohin Singh, Daniel Harrison, Megan Bauman, Andreas Seas, Shane Shahrestani, Julian Gendreau, Oren Gottfried   +7 more
doaj   +1 more source

Moyamoya disease and alternating hemiplegia. A report of two cases

The Turkish Journal of Pediatrics, 1993
Moyamoya disease is one of the cerebrovascular disorders and is characterized by bilateral stenosis or occlusion of the distal internal carotid arteries and their main branches. Repeated ischemic episodes in children and intracranial hemorrhage in
Y Renda, K Gücüyener, H Ozen, M Topçu
doaj   +2 more sources

Genetics and Biomarkers of Moyamoya Disease: Significance of as a Susceptibility Gene [PDF]

Journal of Stroke, 2014
Moyamoya disease is characterized by a progressive stenosis at the terminal portion of the internal carotid artery and an abnormal vascular network at the base of the brain.
Miki Fujimura, Shinya Sonobe, Yasuo Nishijima, Kuniyasu Niizuma, Hiroyuki Sakata, Shigeo Kure, Teiji Tominaga   +6 more
doaj   +1 more source

Case report: Steroid-responsive acute chorea as first presentation of the coexistence of Moyamoya and Graves' disease

Frontiers in Neurology, 2023
BackgroundChorea is a movement disorder characterized by abrupt, rapid, and uncontrollable, random movements from one part of the body to another with motor impersistence. Sporadic chorea is rarely caused by either thyrotoxicosis or Moyamoya disease (MMD)
Wei-Sheng Wang, Shey-Lin Wu, Shey-Lin Wu, Wei-Chieh Chan, Yen-Chung Chen, Yen-Chung Chen   +5 more
doaj   +1 more source

Moyamoya syndrome presenting in an adult with Down syndrome: A case report with a literature review

Radiology Case Reports, 2022
Moyamoya disease is an unusual occlusive cerebrovascular condition commonly seen in children, marked by stenosis of the internal carotid artery and circle of Willis, causing, cerebral ischemia.
Mohamed Hamid, MD, Soukaina Cherradi, MD, Ahmed Bourazza, MD   +2 more
doaj   +1 more source

Pediatric moyamoya disease presenting with intracerebral hemorrhage--report of three cases and review of the literature. [PDF]

, 2008
Intracerebral hemorrhage in patients with moyamoya disease is rare in children. We report three unique cases of pediatric moyamoya disease with hemorrhagic onset.
Nagata, Izumi, Suyama, Kazuhiko, Ishikawa, Yasunari, Takahata, Hideaki, Yoshida, Koichi, Baba, Hiroshi, Hirose, Makoto, Toda, Keisuke   +7 more
core   +1 more source

Two adolescent patients with coexistent Graves' disease and Moyamoya disease in Korea [PDF]

Korean Journal of Pediatrics, 2014
Moyamoya disease is a cerebrovascular condition that results in the narrowing of the vessels of the circle of Willis and collateral vessel formation at the base of the brain. Although relationships between Graves' disease and cerebrovascular accidents in
Chong Kun Cheon, Su Yung Kim, Jae-Ho Yoo
doaj   +1 more source