Results 91 to 100 of about 10,915 (215)
Moyamoya disease is a rare progressive occlusive cerebrovascular disorder of unknown aetiology, characterised by bilateral narrowing and occlusion of the internal carotid arteries.
M, Prabhu +4 more
openaire +2 more sources
Moyamoya disease and syndromes: from genetics to clinical management
Stéphanie Guey,1,3 Elisabeth Tournier-Lasserve,1,2 Dominique Hervé,1,3 Manoelle Kossorotoff4 1Inserm UMR-S1161, Université Paris 7 Denis Diderot, Sorbonne Paris Cité, Paris, France; 2AP-HP, Groupe hospitalier Lariboisiè ...
Tournier-Lasserve E +3 more
core
Mood disorder in association with moyamoya disease
MOYAMOYA DISEASE IS an inherited vaso-occlusive disease in which dilated collateral vessels appear hazy on angiography.1 Neuropsychiatric manifestations associated with moyamoya disease are uncommon.2 We describe a case of a 16-year-old boy with atypical
Behere, Rishikesh V. +13 more
core +1 more source
Moyamoya disease and syndrome: a review
Moyamoya disease is a chronic occlusive cerebrovascular disease that is non-inflammatory and non-atherosclerotic. It is characterized by endothelial hyperplasia and fibrosis of the intracranial portion of the carotid artery and its proximal branches ...
Luana A. Maranha Gatto (5379989) +5 more
core +1 more source
Low PNI indicates an increased risk of stroke‐associated pneumonia in elderly patients with spontaneous intracerebral hemorrhage. Early assessment of albumin and lymphocytes may help identify high‐risk patients and guide targeted nutritional, respiratory, swallowing, and infection‐prevention strategies.
Gang Wang +6 more
wiley +1 more source
Background. We present a rare case of bilateral moyamoya disease presenting as multiple strokes and neurological deficits, treated with the neurosurgical procedure, encephaloduroarteriosynangiosis (EDAS), in a 2-year-old male Pakistani minor.
Shahvaiz Magsi +4 more
doaj +1 more source
Thirty eight cases of moyamoa disease, 21 children, 17 adults were encountered during a 16-year period at Yonsei University Medical Center. Clinical manifestations, together with computed tomography (CT) and angiographic findings were analyzed with a review of the literature.
G J, Yu, S Y, Kim, C J, Coe
openaire +2 more sources
Surgical Therapy for Adult Moyamoya Disease
Background and Purpose It is well recognized that revascularization surgery using direct and/or indirect bypass provides effective surgical management for pediatric moyamoya disease.
Hiroyasu Kamiyama +4 more
core +1 more source
Moyamoya disease and moyamoya syndrome in children : case reports and a literature review
Background: Moyamoya disease is a rare angiopathy (vascular disorder) that leads to a narrowing and occlusion of the distal internal carotid artery and proximal anterior and middle cerebral arteries.
Homa, Jarosław +5 more
core +1 more source
Moyamoya disease associated with polycystic kidney disease and eosinophilic granuloma.
Moyamoya disease has been associated with renal artery stenosis, cerebral hemorrhage, and multiple cranial traumas. We report a unique case of moyamoya disease associated with polycystic kidney disease and eosinophilic granuloma. Although the etiology of
J M Massey, J B Pracyk
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