Results 31 to 40 of about 5,183,178 (176)
PLoS 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
Clinical and radiological recurrence after childhood arterial ischemic stroke [PDF]
, 2006 Background: Data on rates and risk factors for clinical and radiological recurrence of childhood arterial ischemic stroke (AIS) might inform secondary prevention strategies.
Wade, Angela +7 more
core +1 more source
Single-cell sequencing analysis of peripheral blood in patients with moyamoya disease
Orphanet 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
Frontiers in Neurology, 2021 Moyamoya disease is an idiopathic chronically progressive cerebrovascular disease, which causes both ischemic and hemorrhagic stroke. Genetic studies identified RNF213/Mysterin and GUCY1A3 as disease-causing genes.
Yohei Mineharu, Susumu Miyamoto
doaj +1 more source
Moyamoya Disease, Which is Rare in Infancy: A Case Report
, 2023 Moyamoya disease etiology is an undetermined vasculopathy and is mainly thought to affect the Internal Carotid Artery and Wills circle. An 8-month-old patient without any underlying disease was referred to our hospital with sudden extreme right ...
Derya Bako +3 more
core +1 more source
The course and outcome of unilateral intracranial arteriopathy in 79 children with ischaemic stroke [PDF]
, 2009 Arteriopathies are the commonest cause of arterial ischaemic stroke (AIS) in children. Repeated vascular imaging in children with AIS demonstrated the existence of a 'transient cerebral arteriopathy' (TCA), characterized by lenticulostriate infarction ...
Kirkham, F. J. +10 more
core +1 more source
Characterization of Moyamoya Disease
, 2022 This study will attempt to characterize moyamoya disease (MMD) from ischemic strokes of other ...
Arash
core +1 more source
Moyamoya in Hispanics: not only in Japanese
Neurology International, 2014 Moyamoya disease was first described in 1957 as hypoplasia of the bilateral internal carotid arteries, the characteristic appearance of the associated network of abnormally dilated collateral vessels on angiography was later likened to something hazy ...
Sarmad Said +5 more
doaj +1 more source
Successful Regional Anesthetic for a Parturient with Moyamoya Syndrome
Case Reports in Anesthesiology, 2020 Anesthesia for Cesarean section could be challenging due to the physiological changes during pregnancy, but it can be more complicated if associated with sickle cell disease and moyamoya disease.
Anjalena Pasam +4 more
doaj +1 more source
RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients. [PDF]
PLoS ONE, 2016 RNF213/Mysterin has been identified as a susceptibility gene for moyamoya disease, a cerebrovascular disease characterized by occlusive lesions in the circle of Willis.
Hatasu Kobayashi +19 more
doaj +1 more source