Results 21 to 30 of about 15,917 (214)
Asymptomatic Moyamoya Disease [PDF]
To the Editor: We read with great interest the article by Kuroda et al1 concerning asymptomatic moyamoya disease (MMD) in multicenter survey. The authors describe clinic-radiological findings in 40 patients. We also reported asymptomatic MMD adults on brain check-up (BC)–based population in Japan.2 A total of 11 402 healthy subjects (7570 men and 3832
Ken, Ikeda +4 more
openaire +2 more sources
Experimental study of the pathogenesis of moyamoya disease: histological changes in the arterial wall caused by immunological reactions in monkeys. [PDF]
Moyamoya disease is a progressive vascular disorder of unknown etiology. Theories of inflammatory and immunologic mechanisms have been proposed as the pathogeneses.
Kamata, Ichiro +2 more
core +1 more source
Moyamoya: A Review of the Disease and Current Treatments [PDF]
INTRODUCTION Moyamoya disease is a rare progressive cerebrovascular disease characterized by bilateral stenosis of vasculature of the Circle of Willis, specifically the distal internal carotid arteries, that leads to extensive collateral circulation ...
Anderson, Eliza +6 more
core +2 more sources
Successful Regional Anesthetic for a Parturient with Moyamoya Syndrome
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
Aneurysms of the intracranial segment of the ophthalmic artery trunk. case report and systematic literature review [PDF]
Aneurysms arising from the ophthalmic artery trunk (OAT) are very rare, particularly in the artery's intracranial course. The onset of a subarachnoid hemorrhage (SAH) from a ruptured OAT aneurysm in this segment is extremely rare.
C. Colonnese +5 more
core +1 more source
Pediatric Moyamoya disease [PDF]
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
Moyamoya syndrome is a rare chronic progressive disease of brain vessels in which certain arteries in the brain are constricted. During the disease a collateral circulation develops around the blocked vessels to compensate for the blockage, and on angiography these collateral vessels have the appearance of a "puff of smoke".
K I, Burkova +7 more
+5 more sources
Moyamoya Disease with Coexistent Hypertriglyceridemia in Pediatric Patient
Moyamoya disease is a rare chronic and progressive cerebrovascular disease of the arteries of the circle of Willis that can affect children and adults. It has been associated with multiple diseases, including immunologic, like Graves’ disease, diabetes ...
Jacqueline Chan +3 more
doaj +1 more source
RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients. [PDF]
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
Unilateral moyamoya disease with co-existing arteriovenous malformation [PDF]
A case of an intracerebral bleed in a young man with a rare combination of arteriovenous malformation (AVM) and unilateral moyamoya disease is presented.
Mohd Ramli, Norlisah +2 more
core +1 more source

