Results 11 to 20 of about 21,247 (273)

Pediatric Moyamoya Disease in Nepal and Challenges in a Resource‐Limited Setting: A Case Report [PDF]

Clinical Case Reports, Volume 13, Issue 10, October 2025.
ABSTRACT Moyamoya disease (MMD) is a rare progressive cerebrovascular disorder characterized by stenosis of the terminal internal carotid arteries with fragile collateral vessel formation. It is common in East Asia but underreported in Nepal. Pediatric cases typically present with ischemic symptoms such as transient ischemic attacks, stroke, or ...
Kapil Khanal, Sunil Dhungana, Bindu Gyawali, Rishab Khanal, Binit Bajracharya, Nishant Neupane, Nijan Sharma, Kailash Mani Pokhrel, Manish Acharya, Shreya Sinha   +9 more
wiley   +2 more sources

Research progress in unilateral moyamoya disease [PDF]

Frontiers in Human Neuroscience
Unilateral moyamoya disease (U-MMD) is a chronic vascular disease characterized by progressive stenosis and occlusion of the terminal end of the internal carotid artery and its main branches, resulting in the appearance of moyamoya-like blood vessels at ...
Xiaokuan Hao, Cunxin Tan, Ziqi Liu, Yang Tie, Yanru Wang, Shihao He, Ran Duan, Rong Wang, Rong Wang   +8 more
doaj   +2 more sources

Moyamoya disease [PDF]

Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova, 2016
Moya-moya is a rare cerebrovascular disease characterized by the progressive occlusion of cerebral vessels with partial switching off the circle of Willis and arteries that feed it. The article provides a review of literature, modern diagnostic criteria and a description of a single clinical case.
Esin R., Isayeva Y., Gorobets E., Tokareva N., Esin O.   +4 more
  +11 more sources

Increased Autoimmunity in Individuals With Down Syndrome and Moyamoya Disease

Frontiers in Neurology, 2021
Objective: To determine if elevated rates of autoimmune disease are present in children with both Down syndrome and moyamoya disease given the high rates of autoimmune disease reported in both conditions and unknown etiology of angiopathy in this ...
Jonathan D. Santoro, Jonathan D. Santoro, Sarah Lee, Anthony C. Wang, Eugenia Ho, Eugenia Ho, Deepti Nagesh, Deepti Nagesh, Mellad Khoshnood, Runi Tanna, Ramon A. Durazo-Arvizu, Melanie A. Manning, Melanie A. Manning, Brian G. Skotko, Brian G. Skotko, Gary K. Steinberg, Michael S. Rafii, Michael S. Rafii   +17 more
doaj   +1 more source

Diagnostic Criteria for Moyamoya Disease - 2021 Revised Version

Neurologia Medico-Chirurgica, 2022
In this report, we, the Research Committee on Moyamoya Disease (Spontaneous Occlusion of the circle of Willis), describe in detail the changes in the new “Diagnostic Criteria 2021” for moyamoya disease and its scientific basis to make it widely known to ...
Satoshi KURODA, Miki FUJIMURA, Jun TAKAHASHI, Hiroharu KATAOKA, Kuniaki OGASAWARA, Toru IWAMA, Teiji TOMINAGA, Susumu MIYAMOTO, The Research Committee on Moyamoya Disease (Spontaneous Occlusion of Circle of Willis) of the Ministry of Health, Labor, and Welfare, Japan   +8 more
doaj   +1 more source

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

Moyamoya Disease [PDF]

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2000
Moyamoya disease is a specific chronic cerebrovascular occlusive disease first reported by Japanese surgeons in 1957. The disease is characterized by stenosis or occlusion of the terminal portions of the bilateral internal carotid arteries and abnormal vascular network in the vicinity of the arterial occlusion. It may cause ischemic attacks or cerebral
I, Fleetwood, G K, Steinberg
openaire   +4 more sources

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