医中誌リンクサービス


文献リスト

1)Wakai K, Tamakoshi A, Ikezaki K, et al. Epidemiological features of moyamoya disease in Japan: findings from a nationwide survey. Clin Neurol Neurosurg. 1997; 99 Suppl 2: S1-5
PubMed
医中誌リンクサービス
2)Kuriyama S, Kusaka Y, Fujimura M, et al. Pre-valence and clinicoepidemiological features of moyamoya disease in Japan: findings from a nationwide epidemiological survey. Stroke. 2008; 39: 42-7
PubMed CrossRef
医中誌リンクサービス
3)Baba T, Houkin K, Kuroda S. Novel epidemiological features of moyamoya disease. J Neurol Neurosurg Psychiatry. 2008; 79: 900-4
PubMed CrossRef
医中誌リンクサービス
4)Mineharu Y, Takenaka K, Yamakawa H, et al. Inheritance pattern of familial moyamoya disease: autosomal dominant mode and genomic imprinting. J Neurol Neurosurg Psychiatry. 2006; 77: 1025-9
PubMed CrossRef
医中誌リンクサービス
5)Fukui M, Kono S, Sueishi K, et al. Moyamoya disease. Neuropathology. 2000; 20 Suppl: S61-4
PubMed
医中誌リンクサービス
6)Nanba R, Kuroda S, Tada M, et al. Clinical features of familial moyamoya disease. Childs Nerv Syst. 2006; 22: 258-62
PubMed CrossRef
医中誌リンクサービス
7)Goto Y, Yonekawa Y. Worldwide distribution of moyamoya disease. Neurol Med Chir (Tokyo). 1992; 32: 883-6
医学中央雑誌刊行会  PubMed CrossRef J-Stage
医中誌リンクサービス
8)Suzuki J, Kodama N. Moyamoya disease--a review. Stroke. 1983; 14: 104-9
PubMed CrossRef
医中誌リンクサービス
9)Yonekawa Y, Ogata N, Kaku Y, et al. Moyamoya disease in Europe, past and present status. Clin Neurol Neurosurg. 1997; 99 Suppl 2: S58-60
PubMed
医中誌リンクサービス
10)Kuroda S, Houkin K. Moyamoya disease: current concepts and future perspectives. Lancet Neurol. 2008; 7: 1056-66
PubMed CrossRef
医中誌リンクサービス
11)Ikeda H, Sasaki T, Yoshimoto T, et al. Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Am J Hum Genet. 1999; 64: 533-7
PubMed CrossRef
医中誌リンクサービス
12)Sakurai K, Horiuchi Y, Ikeda H, et al. A novel susceptibility locus for moyamoya disease on chromosome 8q23. J Hum Genet. 2004; 49: 278-81
医学中央雑誌刊行会  PubMed CrossRef
医中誌リンクサービス
13)Mineharu Y, Liu W, Inoue K, et al. Autosomal dominant moyamoya disease maps to chromosome 17q25.3. Neurology. 2008; 70: 2357-63
PubMed CrossRef
医中誌リンクサービス
14)Inoue TK, Ikezaki K, Sasazuki T, et al. Linkage analysis of moyamoya disease on chromosome 6. J Child Neurol. 2000; 15: 179-82
PubMed CrossRef
医中誌リンクサービス
15)Guo DC, Papke CL, Tran-Fadulu V, et al. Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moya-moya disease, along with thoracic aortic disease. Am J Hum Genet. 2009; 84: 617-27
PubMed CrossRef
医中誌リンクサービス
16)Shimojima K, Yamamoto T. ACTA2 is not a major disease-causing gene for moyamoya disease. J Hum Genet. 2009; 54: 687-8
医学中央雑誌刊行会  PubMed CrossRef
医中誌リンクサービス
17)Miskinyte S, Butler MG, Herve D, et al. Loss of BRCC3 deubiquitinating enzyme leads to abnormal angiogenesis and is associated with syndromic moyamoya. Am J Hum Genet. 2011; 88: 718-28
PubMed CrossRef
医中誌リンクサービス
18)Xin B, Jones S, Puffenberger EG, et al. Homozygous mutation in SAMHD1 gene causes cerebral vasculopathy and early onset stroke. Proc Natl Acad Sci U S A. 2011; 108: 5372-7
PubMed CrossRef
医中誌リンクサービス
19)Roder C, Peters V, Kasuya H, et al. Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patients. Acta Neurochir (Wien). 2010; 152: 2153-60
PubMed CrossRef
医中誌リンクサービス
20)Kang HS, Kim SK, Cho BK, et al. Single nucleotide polymorphisms of tissue inhibitor of metalloproteinase genes in familial moyamoya disease. Neurosurgery. 2006; 58: 1074-80; discussion -80
PubMed CrossRef
医中誌リンクサービス
21)Liu W, Hashikata H, Inoue K, et al. A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians. Environ Health Prev Med. 2010; 15: 94-104
医学中央雑誌刊行会  CrossRef
医中誌リンクサービス
22)Yamauchi T, Tada M, Houkin K, et al. Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke. 2000; 31: 930-5
PubMed CrossRef
医中誌リンクサービス
23)Nanba R, Tada M, Kuroda S, et al. Sequence analysis and bioinformatics analysis of chromosome 17q25 in familial moyamoya disease. Childs Nerv Syst. 2005; 21: 62-8
PubMed CrossRef
医中誌リンクサービス
24)Kamada F, Aoki Y, Narisawa A, et al. A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. J Hum Genet. 2011; 56: 34-40
医学中央雑誌刊行会  PubMed CrossRef
医中誌リンクサービス
25)Liu W, Morito D, Takashima S, et al. Identification of RNF213 as a susceptibility gene for moya-moya disease and its possible role in vascular Development. PloS One. 2011; 6: e22542
CrossRef
医中誌リンクサービス
26)Miyatake S, Miyake N, Touho H, et al. Homozygous c. 14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease. Neurology. 2012; 78: 803-10
PubMed CrossRef
医中誌リンクサービス
27)Lupas AN, Martin J. AAA proteins. Curr Opin Struct Biol. 2002; 12: 746-53
PubMed CrossRef
医中誌リンクサービス
28)Miyawaki S, Imai H, Takayanagi S, et al. Identification of a genetic variant common to moyamoya disease and intracranial major artery stenosis/occlusion. Stroke. 2012; 43: 3371-4
PubMed CrossRef
医中誌リンクサービス
29)Koizumi A, Kobayashi H, Liu W, et al. P. R4810K, a polymorphism of RNF213, the susceptibility gene for moyamoya disease, is associated with blood pressure. Environ Health Prev Med. 2013; 18: 121-9
医学中央雑誌刊行会  PubMed CrossRef
医中誌リンクサービス
30)Eichler EE, Flint J, Gibson G, et al. Missing heritability and strategies for finding the underlying causes of complex disease. Nat Rev Genet. 2010; 11: 446-50
PubMed CrossRef
医中誌リンクサービス
31)Manolio TA, Collins FS, Cox NJ, et al. Finding the missing heritability of complex diseases. Nature. 2009; 461: 747-53
PubMed CrossRef
医中誌リンクサービス
32)Miyatake S, Touho H, Miyake N, et al. Sibling cases of moyamoya disease having homozygous and heterozygous c. 14576G>A variant in RNF213 showed varying clinical course and severity. J Hum Genet. 2012; 57: 804-6
医学中央雑誌刊行会  PubMed CrossRef
医中誌リンクサービス
33)Kim SK, Cho BK, Phi JH, et al. Pediatric moya-moya disease: An analysis of 410 consecutive cases. Ann Neurol. 2010; 68: 92-101
PubMed CrossRef
医中誌リンクサービス
34)Yamada I, Himeno Y, Suzuki S, et al. Posterior circulation in moyamoya disease: angiographic study. Radiology. 1995; 197: 239-46
PubMed
医中誌リンクサービス
35)Kim SK, Seol HJ, Cho BK, et al. Moyamoya disease among young patients: its aggressive clinical course and the role of active surgical treatment. Neurosurgery. 2004; 54: 840-4
PubMed CrossRef
医中誌リンクサービス
36)Mugikura S, Higano S, Shirane R, et al. Posterior circulation and high prevalence of ischemic stroke among young pediatric patients with Moya-moya disease: evidence of angiography-based differences by age at diagnosis. AJNR Am J Neuroradiol. 2011; 32: 192-8
PubMed
医中誌リンクサービス
37)Southerland AM, Meschia JF, Worrall BB. Shared associations of nonatherosclerotic, large-vessel, cerebrovascular arteriopathies: considering intracranial aneurysms, cervical artery dissection, moyamoya disease and fibromuscular dysplasia. Curr Opin Neurol. 2013; 26: 13-28
PubMed CrossRef
医中誌リンクサービス


NPO医学中央雑誌刊行会
https://www.jamas.or.jp/
info@jamas.or.jp