Results 41 to 50 of about 10,915 (215)
Research progress on the inflammatory pathogenesis of moyamoya disease
Moyamoya disease is a specific cerebrovascular disease characterized by progressive narrowing of the terminal part of the internal carotid artery and its major branches, and these changes lead to chronic cerebrovascular occlusion and the formation of an ...
Chaojue HUANG +4 more
doaj +1 more source
Coexistence of Chiari 2 malformation and moyamoya syndrome in a 17-year-old girl. [PDF]
A 17-year-old female with Chiari 2 malformation developed cerebral infarction with angiographically typical bilateral moyamoya vessels manifesting as sudden onset of moderate left hemiparesis.
Nagata, Izumi +5 more
core +1 more source
Updates in the management of moyamoya disease
Moyamoya is a rare, steno-occlusive cerebrovascular disorder that often presents as ischemic or hemorrhagic intracerebral events. This review provides an overview of various surgical revascularization techniques used in treating Moyamoya disease ...
Angie Zhang +5 more
doaj +1 more source
Early manifestation of Moyamoya syndrome in a 2-year-old child with Down syndrome
Moyamoya is a rare occlusive cerebrovascular disease characterized by progressive stenosis of the terminal portion of the internal carotid artery and the circle of Willis.
Abasin Tajmalzai, MD +2 more
doaj +1 more source
Safety of antiplatelet therapy during the perioperative period of revascularization surgery for moyamoya disease patients with ischemic onset [PDF]
For patients with moyamoya disease, antiplatelet agents are often used during the perioperative periods of revascularization surgeries to prevent ischemic events.
Nakamura, Akihiro +3 more
core +1 more source
Objective: We report a 7 year-old boy, known case of sickle cell disease, who underwent laparoscopic cholecystectomy for gallstones. He sustained brain insult due to undiagnosed MoyaMoya syndrome.
Jamal Al Hudhaif +3 more
doaj +1 more source
ABSTRACT Heterozygous germline variants in CBL disrupt its function as a negative regulator of the Ras/MAPK pathway, classically predisposing to Juvenile myelomonocytic leukemia (JMML) and moyamoya. We describe two affected siblings carrying a paternally inherited CBL variant (c.1210 T> C, p.
Michal Bar‐Hakim +12 more
wiley +1 more source
The marked cerebral hypoperfusion of moyamoya disease (MMD) can be treated with encephaloduroarteriosynangiosis (EDAS), an indirect revascularization surgery.
Yeh, Shin-Joe;Tang, Sung-Chun;Tsai, Li-Kai;Chen, Ya-Fang;Liu, Hon-Man;Chen, Ying-An;Hsieh, Yu-Lin;Yang, Shih-Hung;Tien, Yu-Hsuan;Yang, Chi-Cheng;Kuo, Meng-Fai;Jeng, Jiann-Shing +1 more
core +1 more source
Characterization of Moyamoya Disease
This study will attempt to characterize moyamoya disease (MMD) from ischemic strokes of other ...
Arash
core +1 more source
Moyamoya Syndrome: A Window of Moyamoya Disease
Moyamoya-like vasculopathy develops in association with various systemic diseases and conditions, which is termed moyamoya syndrome. Relatively common diseases and conditions are related to moyamoya syndrome, including neurofibromatosis type 1, Down syndrome, thyroid disease, and cranial irradiation.
Phi, Ji Hoon +3 more
openaire +2 more sources

