Results 81 to 90 of about 10,915 (215)
Mutation genotypes of RNF213 gene from moyamoya patients in Taiwan
, 2017 Moyamoya disease (MMD) is a disorder characterized by stenosis of bilateral internal carotid arteries with compensatory angiogenesis of the perforating blood vessels. Familial transmission in MMD is common.
陳雅芳;范碧娟;郭夢菲;李銘仁;王國川 +1 more
core +1 more source
Respirology Case Reports, Volume 14, Issue 6, June 2026.This report describes a practical adjunct to bronchoscopy‐guided percutaneous dilatational tracheostomy: a two‐step method in which an individualized endotracheal tube withdrawal distance is estimated using bronchoscopic transillumination and subsequently used as a quantitative target during tube repositioning, with real‐time confirmation at the ...
Yuya Aoki, Masaki Kono, Takuo Yoshida
wiley +1 more source
Environmental Health and Preventive Medicine, 2017 Objectives RNF213 p.R4810K was identified as a susceptibility variant for moyamoya disease in Asia and non-moyamoya intracranial artery stenosis/occlusion disease in Japan and Korea recently.
Tong Zhang +6 more
doaj +1 more source
Moyamoya Disease in Europeans [PDF]
Stroke, 2008 Background and Purpose— We describe the clinical, diagnostic, and outcome features of a cohort of white patients with idiopathic moyamoya disease treated in a German institution. Methods— Our cohort included 21 white patients ...
Markus, Kraemer +2 more
openaire +2 more sources
Moyamoya disease and anesthesia
, 2005 Moyamoya disease is a condition that results from bilateral stenosis or obstruction of the intracranial arteries at the base of the brain. Patients exhibit ischemic symptoms, and vascular reconstruction is the therapy of choice.
DAĞÇINAR, ADNAN
core +1 more source
Pediatric Moyamoya disease [PDF]
American Journal of Case Reports, 2013 Moyamoya disease (MMD) is a progressive cerebrovascular occlusive disease of the bilateral internal carotid arteries that leads to a compensatory abnormal vascular network at the base of the brain. Its average annual incidence 0.54 per 100,000 population but it is the most common pediatric cerebrovascular disease in East Asia. The reported incidence in
Nagiub, Mohamed, Allarakhia, Iqbal
openaire +2 more sources
European Journal of Neurology, Volume 33, Issue 6, June 2026.In this European cohort of 276 patients with Moyamoya angiopathy, surgical revascularization, predominantly combined bypass surgery targeting the MCA territory via a mini‐craniotomy, was associated with low perioperative complication rates (6.3%) and stroke rates (2.6%).
Robert Mertens +10 more
wiley +1 more source
JOURNAL of CLINICAL AND DIAGNOSTIC RESEARCH, 2013 Moyo Moya Disease (MMD) is a rare, progressively stenotic condition of the intracranial arteries with various cerebrovascular manifestations. Ocular manifestations are seen very rarely and there are only few case reports of ocular perfusion anomalies. Central Retinal Artery Occlusion (CRAO) can be caused by atherosclerosis related thrombosis, carotid ...
Ashok Kumar M., Amirtha Ganesh B.
openaire +3 more sources
, 2016 OBJECTIVE Dysexecutive syndrome is common in patients with moyamoya disease (MMD), a chronic cerebrovascular disease that is characterized by stenosis of the bilateral internal carotid arteries and progressive collateral revascularization, and MMD can ...
Chan, Raymond C. K. +12 more
core +1 more source
Brain and Behavior, Volume 16, Issue 5, May 2026.Elevated lipoprotein(a) is independently associated with poor 3‐month outcomes in acute ischemic stroke. Combining Lp(a) with NIHSS improves prognostic accuracy. ABSTRACT Background Lipoprotein(a) (Lp(a)) is a known cardiovascular risk factor, but its role in acute ischemic stroke (AIS) prognosis remains unclear. This study investigated the association
Xinyi Chen +5 more
wiley +1 more source