Results 181 to 190 of about 13,974 (214)
Some of the next articles are maybe not open access.
Moyamoya Disease and Moyamoya Syndrome
New England Journal of Medicine, 2009Moyamoya disease is a cerebrovascular condition predisposing affected patients to stroke in association with progressive stenosis of the intracranial internal carotid arteries and their proximal branches. Patients with characteristic moyamoya vasculopathy plus associated conditions are categorized as having moyamoya syndrome.
R Michael Scott
exaly +6 more sources
Child's Nervous System, 1988
The authors reviewed the Japanese literature on moyamoya disease. In the article we discuss the history of such investigations in Japan, the signs and symptoms, the diagnosis (especially concerning diagnostic criteria and magnetic resonance imaging), the pathology in relation to its etiology, and the current methods of treatment. On the whole, the main
Y, Maki, T, Enomoto
openaire +2 more sources
The authors reviewed the Japanese literature on moyamoya disease. In the article we discuss the history of such investigations in Japan, the signs and symptoms, the diagnosis (especially concerning diagnostic criteria and magnetic resonance imaging), the pathology in relation to its etiology, and the current methods of treatment. On the whole, the main
Y, Maki, T, Enomoto
openaire +2 more sources
Journal of Neurosurgery: Pediatrics, 2007
Abstract: Object. The authors' aim in this Study was to review their experience in the use of indirect revascularization alone in a series of 14 children with moyamoya disease, in which numerous bur holes and arachnoid openings were made over each affected hemisphere. Methods.
Menovsky, Tomas, De Ridder, Dirk
openaire +2 more sources
Abstract: Object. The authors' aim in this Study was to review their experience in the use of indirect revascularization alone in a series of 14 children with moyamoya disease, in which numerous bur holes and arachnoid openings were made over each affected hemisphere. Methods.
Menovsky, Tomas, De Ridder, Dirk
openaire +2 more sources
No shinkei geka. Neurological surgery, 2021
In this educational article for young neurosurgeons, the author highlights the characteristic CT and MRI findings for diagnosing moyamoya disease. The author also provides guidelines for the systematic interpretation of angiographic findings in patients with moyamoya disease.
null Leonard Tiong, MBBS +1 more
openaire +3 more sources
In this educational article for young neurosurgeons, the author highlights the characteristic CT and MRI findings for diagnosing moyamoya disease. The author also provides guidelines for the systematic interpretation of angiographic findings in patients with moyamoya disease.
null Leonard Tiong, MBBS +1 more
openaire +3 more sources
Is “unilateral” moyamoya disease different from moyamoya disease?
Journal of Neurosurgery, 1996✓ Whether a diagnosis of moyamoya disease is justified in patients with typical angiographic evidence of moyamoya disease unilaterally and normal angiographic findings contralaterally remains controversial. In this study the authors analyzed longitudinal angiographic change, familial occurrence, and basic fibroblast growth factor (bFGF) concentration ...
K, Houkin +3 more
openaire +2 more sources
Cerebrovascular Moyamoya disease
European Journal of Pediatrics, 1984Clinical features of ten Japanese children with cerebrovascular Moyamoya disease are reported and non-Japanese paediatric cases of the disease are reviewed from the world literature. The most common initial manifestations were headache in four cases (40%), motor deficit and convulsion in three cases (30%).
Y, Yamashiro, H, Takahashi, K, Takahashi
openaire +2 more sources
Clinical Nuclear Medicine, 1995
Tc-99m HMPAO SPECT was used to evaluate regional blood flow in one monozygotic twin who had angiographically proven moyamoya disease. Focal and global reduced regional cerebral perfusion were observed in both patients with Tc-99m HMPAO SPECT studies.
Duman, Y +3 more
openaire +4 more sources
Tc-99m HMPAO SPECT was used to evaluate regional blood flow in one monozygotic twin who had angiographically proven moyamoya disease. Focal and global reduced regional cerebral perfusion were observed in both patients with Tc-99m HMPAO SPECT studies.
Duman, Y +3 more
openaire +4 more sources
Clinical Neurology and Neurosurgery, 2013
Moyamoya disease (MMD) is a unique occlusive disease of the bilateral internal carotid arteries in which, compensation for occlusion results in an enrichment of collateral arteries at the base of the brain. However, the epidemiology of unilateral MMD (typical angiographic evidence of MMD unilaterally with equivocal contralateral findings), and quasi ...
Kentaro, Hayashi +3 more
openaire +2 more sources
Moyamoya disease (MMD) is a unique occlusive disease of the bilateral internal carotid arteries in which, compensation for occlusion results in an enrichment of collateral arteries at the base of the brain. However, the epidemiology of unilateral MMD (typical angiographic evidence of MMD unilaterally with equivocal contralateral findings), and quasi ...
Kentaro, Hayashi +3 more
openaire +2 more sources