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Literature DB >> 9409446

Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis ('moyamoya' disease). Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare, Japan.

M Fukui.

Abstract

Mesh：

Year: 1997 PMID： 9409446

Source DB: PubMed Journal: Clin Neurol Neurosurg ISSN： 0303-8467 Impact factor: 1.876

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117 in total

1. The maya behind moyamoya--the two extremes of the disease.

Authors: Nandini Vijayakanthi; Thillothammal Natarajan
Journal: Indian J Pediatr Date: 2012-06-26 Impact factor: 1.967

2. Clinical features and outcome in North American adults with idiopathic basal arterial occlusive disease without moyamoya collaterals.

Authors: Manu S Goyal; Christopher L Hallemeier; Gregory J Zipfel; Keith M Rich; Robert L Grubb; Michael R Chicoine; Christopher J Moran; DeWitte T Cross; Ralph G Dacey; Colin P Derdeyn
Journal: Neurosurgery Date: 2010-08 Impact factor: 4.654

3. Quantitative Assessment of Neovascularization after Indirect Bypass Surgery: Color-Coded Digital Subtraction Angiography in Pediatric Moyamoya Disease.

Authors: H-H Cho; J-E Cheon; S-K Kim; Y H Choi; I-O Kim; W S Kim; S-M Lee; S K You; S-M Shin
Journal: AJNR Am J Neuroradiol Date: 2015-12-17 Impact factor: 3.825

Review 4. Concurrent Graves' disease and intracranial arterial stenosis/occlusion: special considerations regarding the state of thyroid function, etiology, and treatment.

Authors: Shigeo Ohba; Toru Nakagawa; Hideki Murakami
Journal: Neurosurg Rev Date: 2011-03-19 Impact factor: 3.042

5. 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

6. A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians.

Authors: Wanyang Liu; Hirokuni Hashikata; Kayoko Inoue; Norio Matsuura; Yohei Mineharu; Hatasu Kobayashi; Ken-Ichiro Kikuta; Yasushi Takagi; Toshiaki Hitomi; Boris Krischek; Li-Ping Zou; Fang Fang; Roman Herzig; Jeong-Eun Kim; Hyun-Seung Kang; Chang-Wan Oh; David-Alexandre Tregouet; Nobuo Hashimoto; Akio Koizumi
Journal: Environ Health Prev Med Date: 2009-11-19 Impact factor: 3.674

Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis ('moyamoya' disease). Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare, Japan.

1. The maya behind moyamoya--the two extremes of the disease.

2. Clinical features and outcome in North American adults with idiopathic basal arterial occlusive disease without moyamoya collaterals.

3. Quantitative Assessment of Neovascularization after Indirect Bypass Surgery: Color-Coded Digital Subtraction Angiography in Pediatric Moyamoya Disease.

Review 4. Concurrent Graves' disease and intracranial arterial stenosis/occlusion: special considerations regarding the state of thyroid function, etiology, and treatment.

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

6. A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians.

7. Surgical Revascularization in North American Adults with Moyamoya Phenomenon: Long-Term Angiographic Follow-up.

8. Moyamoya disease in pregnancy: maintenance of maternal blood pressure.

9. Posterior circulation involvement and collateral flow pattern in moyamoya disease with the RNF213 polymorphism.

10. Early-onset stroke with moyamoya-like syndrome and extraneurological signs: a first reported paediatric series.