Results 11 to 20 of about 13,974 (214)

Moyamoya Disease and the Risk of Parkinson's Disease. [PDF]

open access: yesAnn Clin Transl Neurol
ABSTRACT Objectives Moyamoya disease (MMD) is a rare cerebrovascular disorder characterized by the progressive narrowing of arteries at the base of the brain, forming abnormal collateral vascular networks. While vascular parkinsonism is noted in MMD, its link to Parkinson's disease (PD) has not been explored.
Yoo D   +9 more
europepmc   +2 more sources

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

open access: yesBMC 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   +7 more
doaj   +1 more source

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

open access: yesStroke: 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   +7 more
doaj   +1 more source

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

open access: yesJournal 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   +6 more
doaj   +1 more source

Moyamoya disease [PDF]

open access: yesPostgraduate Medical Journal, 1997
Summary Moyamoya disease is a rare cerebrovascular condition of uncertain aetiology commonly affecting young persons. The disease is mainly seen in Japanese patients. We report two cases of moyamoya disease in Caucasian women and review the postulated aetiological factors and associated conditions as well as the spectrum of invasive and ...
M, Farrugia, D C, Howlett, A M, Saks
openaire   +2 more sources

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

open access: yesFrontiers 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   +5 more
doaj   +1 more source

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

open access: yesRadiology 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   +2 more
doaj   +1 more source

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

open access: yesKorean 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

Development and effects of salutogenesis program for adolescents with moyamoya disease: A randomized controlled trial.

open access: yesPLoS ONE, 2023
BackgroundDisease-specific interventions for management and health behavior implementation are needed to improve the health and quality of life of adolescents with moyamoya disease.ObjectiveThis study aimed to develop a program for adolescents with ...
Insun Yeom, Won-Oak Oh
doaj   +1 more source

Single-cell sequencing analysis of peripheral blood in patients with moyamoya disease

open access: yesOrphanet Journal of Rare Diseases, 2023
Background At present, the etiology of moyamoya disease is not clear, and it is necessary to explore the mechanism of its occurrence and development. Although some bulk sequencing data have previously revealed transcriptomic changes in Moyamoya disease ...
Qikai Tang   +11 more
doaj   +1 more source

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