Stroke, Vol 14, 104-109, Copyright © 1983 by American Heart Association
J Suzuki and N Kodama
One hundred cases of Moyamoya disease were encountered between 1961 and
1980. This report describes the clinical characteristics and emphasizes the
angiographic findings and clinical correlation in this disease. Reasons for
the differences in clinical and radiological presentation in children
versus adults are proposed and a possible pathophysiological mechanism is
outlined. Treatment with perivascular sympathectomy and superior cervical
ganglionectomy may be useful but more investigation needs to be carried out
into the pathogenesis of the disease before more definitive therapy is
realized.
ARTICLES
Moyamoya disease--a review
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I.-S. J. Shin, R. Cheng, and G. R. Pordell Striking CT Scan Findings in a Case of Unilateral Moyamoya Disease A Case Report Angiology, August 1, 1991; 42(8): 665 - 671. [Abstract] [PDF] |
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C. M. Rooney, E. M. Kaye, R. M. Scott, R. P. Klucznik, and N. P. Rosman Modified Encephaloduroarteriosynangiosis as a Surgical Treatment of Childhood Moyamoya Disease: Report of Five Cases J Child Neurol, January 1, 1991; 6(1): 24 - 31. [Abstract] [PDF] |
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W. C. Welch, M. McBride, D. K. Kido, and C. N. Nelson Moyamoya Disease in an Infant With Autonomic Dysfunction: Angiographic and MRI Findings J Child Neurol, April 1, 1988; 3(2): 110 - 113. [Abstract] [PDF] |
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H.-K. Yoon, H.-J. Shin, and Y. W. Chang "Ivy Sign" in Childhood Moyamoya Disease: Depiction on FLAIR and Contrast-enhanced T1-weighted MR Images Radiology, May 1, 2002; 223(2): 384 - 389. [Abstract] [Full Text] [PDF] |
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