Literature DB >> 7533268

Follow-up study of patients with "unilateral" moyamoya disease.

T Kawano1, M Fukui, N Hashimoto, Y Yonekawa.   

Abstract

Sixty-four patients with "unilateral" occlusive disease of the circle of Willis were studied to evaluate progression to bilateral disease. Seventeen patients developed bilateral lesions during a period of 1-7 years after the diagnosis of unilateral lesion. Most of these patients had ischemic attack as the initial episode and had repeated attacks before admission. Young children, mostly less than 10 years of age, tended to develop bilateral lesions within 1-2 years, but adults tended to have only a unilateral lesion. Children or young adults with unilateral occlusive lesion of the terminal portion of the internal carotid artery are likely to develop bilateral disease within 1-5 years.

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Year:  1994        PMID: 7533268     DOI: 10.2176/nmc.34.744

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


  12 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.  Early surgical treatment benefits early staged pediatric moyamoya disease--single case report.

Authors:  Go Matsuoka; Yasuo Aihara; Koji Yamaguchi; Tatsuya Ishikawa; Akitsugu Kawashima; Takakazu Kawamata; Yoshikazu Okada
Journal:  Childs Nerv Syst       Date:  2015-04-23       Impact factor: 1.475

4.  Natural history and progression factors of unilateral moyamoya disease in pediatric patients.

Authors:  Eun Kyung Park; Yun-Ho Lee; Kyu-Won Shim; Joong-Uhn Choi; Dong-Seok Kim
Journal:  Childs Nerv Syst       Date:  2011-05-07       Impact factor: 1.475

5.  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

6.  Moyamoya disease in adults: the role of cerebral revascularization.

Authors:  Gregory J Zipfel; Douglas J Fox; Dennis J Rivet
Journal:  Skull Base       Date:  2005-02

7.  Inheritance pattern of familial moyamoya disease: autosomal dominant mode and genomic imprinting.

Authors:  Y Mineharu; K Takenaka; H Yamakawa; K Inoue; H Ikeda; K-I Kikuta; Y Takagi; K Nozaki; N Hashimoto; A Koizumi
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-06-20       Impact factor: 10.154

8.  Pediatric Moyamoya disease.

Authors:  Mohamed Nagiub; Iqbal Allarakhia
Journal:  Am J Case Rep       Date:  2013-05-03

9.  A case of unilateral moyamoya disease suffered from intracerebral hemorrhage due to the rupture of cerebral aneurysm, which appeared seven years later.

Authors:  Kentaro Hayashi; Nobutaka Horie; Izumi Nagata
Journal:  Surg Neurol Int       Date:  2013-01-29

10.  The course and outcome of unilateral intracranial arteriopathy in 79 children with ischaemic stroke.

Authors:  K P J Braun; M M M Bulder; S Chabrier; F J Kirkham; C S P Uiterwaal; M Tardieu; G Sébire
Journal:  Brain       Date:  2008-11-27       Impact factor: 13.501

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