Literature DB >> 1723176

Moyamoya disease developing from unilateral moyamoya disease--case report.

K Kurose1, H Kishi, Y Nishijima.   

Abstract

The authors report a case of unilateral moyamoya disease which developed into moyamoya disease 3 years later. Unilateral moyamoya disease is generally defined as moyamoya disease, but the exact relationship is unknown. In this case, occlusive changes developed in the stenotic carotid fork, and in a similar portion contralaterally which was intact. Follow-up 4-vessel angiography is strongly recommended even for unilateral moyamoya disease.

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Year:  1991        PMID: 1723176     DOI: 10.2176/nmc.31.597

Source DB:  PubMed          Journal:  Neurol Med Chir (Tokyo)        ISSN: 0470-8105            Impact factor:   1.742


  3 in total

1.  Unilateral (probable) moyamoya disease: long-term follow-up of seven cases.

Authors:  Ho Jun Seol; Kyu-Chang Wang; Seung-Ki Kim; Chang Sub Lee; Dong Soo Lee; In-One Kim; Byung-Kyu Cho
Journal:  Childs Nerv Syst       Date:  2005-10-12       Impact factor: 1.475

2.  Adult unilateral moyamoya disease with familial occurrence in two definite cases: a case report and review of the literature.

Authors:  Noboru Kusaka; Takashi Tamiya; Yoshiaki Adachi; Shinji Katayama; Shimpei Namba; Koji Tokunaga; Kenji Sugiu; Isao Date; Takashi Ohmoto
Journal:  Neurosurg Rev       Date:  2005-07-15       Impact factor: 3.042

3.  Rapid progression of unilateral moyamoya disease.

Authors:  Tae-Wan Kim; Bo-Ra Seo; Jae Hyoo Kim; Young Ok Kim
Journal:  J Korean Neurosurg Soc       Date:  2011-01-31
  3 in total

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