J. H. Park, S. Y. Yang, Y. N. Chung, J. E. Kim, S. K. Kim, D. H. Han and B. K. Cho, “Modified Encephaloduroarteriosynangiosis with Bifrontal Encephalogaleoperiosteal Synangiosis for the Treatment of Pediatric Moyamoya Disease. Technical Note,” Journal of Neurosurgery, Vol. 106, No. 3, 2007, pp. 237-242.

has been cited by the following article:

• TITLE: Involuntary Movements Induced and Remitted by Indirect Bypass Surgery in a Patient with Moyamoya Disease

  AUTHORS: Takao Yanagawa, Tetsuyoshi Horiuchi, Yosuke Hara, Yu Fujii, Kazuhiro Hongo

  KEYWORDS: Involuntary Movement; Indirect Bypass Surgery; Moyamoya Disease

  JOURNAL NAME: Open Journal of Modern Neurosurgery, Vol.2 No.4, October 16, 2012

  ABSTRACT: Involuntary movement is an uncommon manifestation of moyamoya disease. We describe a 12-year-old boy who suffered from involuntary movement after the first surgery but it improved dramatically after the second surgery. Initially, the patient underwent an encephalo-duro-arterio-myosynangiosis on the right side and encephalo-duro-periostealsynangiosis on the bifrontal side, which ameliorated his motor weakness in his left upper extremity. However, involuntary movement appeared in his right upper extremity. Secondly, the patient underwent encephalo-duro-arterio-myo-periostealsynangiosis on the left side. Thereafter, the patient’s involuntary movement completely resolved. The involuntary movement might occur due to the unequal distribution of the blood flow in the basal ganglia.