"Moyamoya Disease" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A noninflammatory, progressive occlusion of the intracranial CAROTID ARTERIES and the formation of netlike collateral arteries arising from the CIRCLE OF WILLIS. Cerebral angiogram shows the puff-of-smoke (moyamoya) collaterals at the base of the brain. It is characterized by endothelial HYPERPLASIA and FIBROSIS with thickening of arterial walls. This disease primarily affects children but can also occur in adults.
Descriptor ID |
D009072
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MeSH Number(s) |
C10.228.140.300.200.600 C10.228.140.300.510.200.737 C14.907.137.615 C14.907.253.123.620 C14.907.253.560.200.737
|
Concept/Terms |
Moyamoya Disease- Moyamoya Disease
- Progressive Intracranial Occlusive Arteropathy (Moyamoya)
- Moyamoya Syndrome
- Moya-Moya Disease
- Disease, Moya-Moya
- Moya Moya Disease
- Cerebrovascular Moyamoya Disease
Moyamoya Disease, Primary- Moyamoya Disease, Primary
- Disease, Primary Moyamoya
- Moyamoya Diseases, Primary
- Primary Moyamoya Disease
- Primary Moyamoya Diseases
- Moyamoya Disease, Classic
- Classic Moyamoya Disease
- Disease, Classic Moyamoya
|
Below are MeSH descriptors whose meaning is more general than "Moyamoya Disease".
Below are MeSH descriptors whose meaning is more specific than "Moyamoya Disease".
This graph shows the total number of publications written about "Moyamoya Disease" by people in this website by year, and whether "Moyamoya Disease" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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2017 | 6 | 0 | 6 |
2018 | 4 | 0 | 4 |
2019 | 2 | 0 | 2 |
2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "Moyamoya Disease" by people in Profiles.
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COVID-19 Presenting With Thalamic Hemorrhage Unmasking Moyamoya Angiopathy. Can J Neurol Sci. 2020 11; 47(6):849-851.
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Misdiagnoses and delay of diagnoses in Moyamoya angiopathy-a large Caucasian case series. J Neurol. 2019 May; 266(5):1153-1159.
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GEN-O-MA project: an Italian network studying clinical course and pathogenic pathways of moyamoya disease-study protocol and preliminary results. Neurol Sci. 2019 Mar; 40(3):561-570.
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Epilepsy surgery for a patient with neurofibromatosis type 1 concomitant with moyamoya syndrome. J Clin Neurosci. 2019 Mar; 61:307-310.
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Quantifying Hemodynamic Changes in Moyamoya Disease Based on Two-Dimensional Cine Phase-Contrast Magnetic Resonance Imaging and Computational Fluid Dynamics. World Neurosurg. 2018 Dec; 120:e1301-e1309.
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Efficacy of STA-MCA bypass surgery in moyamoya angiopathy: long-term follow-up of the Caucasian Krupp Hospital cohort with 81 procedures. J Neurol. 2018 Oct; 265(10):2425-2433.
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Moyamoya angiopathy: early postoperative course within 3 months after STA-MCA-bypass surgery in Europe-a retrospective analysis of 64 procedures. J Neurol. 2018 Oct; 265(10):2370-2378.
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Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature. Int J Mol Sci. 2017 Sep 17; 18(9).
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Moyamoya disease: A rare case with an unusual presentation. Neuroradiol J. 2018 06; 31(3):328-329.
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A "wavering puff of smoke": a rare case of moyamoya disease. Neurol Sci. 2017 11; 38(11):2073-2074.