1.Complications Associated with Surgical Treatment of Moyamoya Disease and Their Management.
Hyun Wook LEE ; Seung Chyul HONG
Journal of Korean Neurosurgical Society 2000;29(8):1136-1139
No abstract available.
Moyamoya Disease*
2.Computed tomographic findings of Moyamoya disease.
Dal Mo YANG ; Woo Suk CHOI ; Kyung Nam RYU ; Sun Wha LEE ; Yup YOON
Journal of the Korean Radiological Society 1991;27(1):33-38
No abstract available.
Moyamoya Disease*
3.Moyamoya Disease, Still a Mysterious Disorder.
Journal of Stroke 2016;18(1):1-1
No abstract available.
Moyamoya Disease*
4.Moyamoya Disease, Still a Mysterious Disorder.
Journal of Stroke 2016;18(1):1-1
No abstract available.
Moyamoya Disease*
5.Clinical Observation on Moyamoya Disease in Childhood.
Se Hee HWANG ; Jae Il SOHN ; Yong Seung HWANG
Journal of the Korean Pediatric Society 1990;33(2):178-188
No abstract available.
Moyamoya Disease*
6.A Case of Familial Spondyloenchondrodysplasia with Immune Dysregulation Masquerading as Moyamoya Syndrome
Jin Sook LEE ; Byung Chan LIM ; Ki Joong KIM ; Seung Ki KIM ; Ok Hwa KIM ; Joong Gon KIM ; Sung Gyoo PARK ; Tae Joon CHO ; Jong Hee CHAE
Journal of Clinical Neurology 2019;15(3):407-409
No abstract available.
Moyamoya Disease
7.Familial Occurrence of Moyamoya Disease in a Father and a Son.
Hyo Jung CHOI ; Jae Gon MOON ; Ho Kook LEE ; Do Yun HWANG
Journal of Korean Neurosurgical Society 2003;34(5):461-463
Although moyamoya disease is a clinical entity of unknown cause, considerable evidences suggest that the disease has genetic origins. The disease displays regional and racial differences. Occurrence of the disease within a family suggests that moyamoya disease may have a genetic basis. Familial moyamoya disease involving father and a son is presented and literatures are also reviewed.
Fathers*
;
Humans
;
Moyamoya Disease*
8.A Case of Moyamoya Disease with Focal Seizure.
Man Gee HONG ; Hak Ki KIM ; Kyung Tai WHANG ; Sung Hoon CHO
Journal of the Korean Pediatric Society 1982;25(10):1053-1057
No abstract available.
Moyamoya Disease*
;
Seizures*
9.Rapid Progression of Unilateral Moyamoya Disease.
Tae Wan KIM ; Bo Ra SEO ; Jae Hyoo KIM ; Young Ok KIM
Journal of Korean Neurosurgical Society 2011;49(1):65-67
The detailed clinical characteristics of unilateral moyamoya disease (MMD) have not been fully elucidated. It has been reported that some patients with unilateral MMD progress to bilateral involvement, while others remain with the unilateral variant. In this series, we present a case of unilateral MMD that progressed to bilateral involvement over the course of just one month.
Humans
;
Moyamoya Disease
10.Moyamoya disease in Korea.
Kyoung Hwa PARK ; Byoung Ho CHA ; Jun Su LEE ; Chang Jun COE
Journal of the Korean Child Neurology Society 1993;1(2):56-63
No abstract available.
Korea*
;
Moyamoya Disease*
Result Analysis
Print
Save
E-mail