Etiology and pathogenesis of Moyamoya Disease: An update on disease prevalence.
Int J Stroke. 2017.
PMID: 28381201
Review.
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biology and pathogenesis of moyamoya disease: an update on disease prevalence
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Etiology and pathogenesis of Moyamoya Disease: An update on disease prevalence.
Int J Stroke. 2017 Apr;12(3):246-253. doi: 10.1177/1747493017694393. Epub 2017 Jan 1.
Int J Stroke. 2017.
PMID: 28381201
Review.
The occurrence of Moyamoya disease is related to immune, genetic, and other factors. Though the research of Moyamoya disease has made great strides in the past 60 years, the etiology and pathogenesis are largely unknown. ...
The occurrence of Moyamoya disease is related to immune, genetic, and other factors. Though the research of Moyamoya …
Moyamoya Disease: A Review of Clinical Research.
Acta Med Okayama. 2016 Aug;70(4):229-36. doi: 10.18926/AMO/54497.
Acta Med Okayama. 2016.
PMID: 27549666
Free article.
Review.
About 5 decades have passed since the concept of moyamoya disease (MMD) was established in Japan. In that time, many clinical MMD studies have been performed from several different points of view, such as epidemiology, pathophysiology, surgical procedures, an …
About 5 decades have passed since the concept of moyamoya disease (MMD) was established in Japan. In that time, many clinical …
A new horizon of moyamoya disease and associated health risks explored through RNF213.
Environ Health Prev Med. 2016 Mar;21(2):55-70. doi: 10.1007/s12199-015-0498-7. Epub 2015 Dec 10.
Environ Health Prev Med. 2016.
PMID: 26662949
Free PMC article.
Review.
The cerebrovascular disorder moyamoya disease (MMD) was first described in 1957 in Japan, and is typically considered to be an Asian-specific disease. ...We also emphasize the importance of a more updated definition for MMD, of qualified cohort studies …
The cerebrovascular disorder moyamoya disease (MMD) was first described in 1957 in Japan, and is typically considered to be an …
Moyamoya disease: current concepts and future perspectives.
Lancet Neurol. 2008 Nov;7(11):1056-66. doi: 10.1016/S1474-4422(08)70240-0.
Lancet Neurol. 2008.
PMID: 18940695
Review.
The incidence of moyamoya disease is high in east Asia, and familial forms account for about 15% of patients with this disease. ...Recent updates and future perspectives for moyamoya disease will also be discussed....
The incidence of moyamoya disease is high in east Asia, and familial forms account for about 15% of patients with this dise …
Vascular risk profile and changes of arterial hypertension after surgical revascularization in adult Moyamoya patients.
Sci Rep. 2024 May 29;14(1):12364. doi: 10.1038/s41598-024-61966-8.
Sci Rep. 2024.
PMID: 38811635
Free PMC article.
Moyamoya disease (MMD) is a rare stenoocclusive cerebral vasculopathy often treated by neurosurgical revascularization using extracranial-intracranial bypasses to prevent ischemic or hemorrhagic events. ...We therefore analyzed 133 adult MMD patients and compared th …
Moyamoya disease (MMD) is a rare stenoocclusive cerebral vasculopathy often treated by neurosurgical revascularization using e …
[Operative neurosurgery: personal view and historical backgrounds (9) Moyamoya angiopathy (MMA): past history and status presens].
No Shinkei Geka. 2012 Jan;40(1):67-87.
No Shinkei Geka. 2012.
PMID: 22223526
Japanese.
Who was the person who discovered this disease. 2. How has the Research Committee of the Ministry of Health and Welfare, Japan (RCMHWJ) contributed to clarify the epidemiology, etiology, pathophysiology and treatments. 3. ...Kudo who described "spontaneous oc …
Who was the person who discovered this disease. 2. How has the Research Committee of the Ministry of Health and Welfare, Japan (RCMHW …
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