Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 93

1.

Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans.

Roder C, Peters V, Kasuya H, Nishizawa T, Takehara Y, Berg D, Schulte C, Khan N, Tatagiba M, Krischek B.

Childs Nerv Syst. 2011 Feb;27(2):245-52. doi: 10.1007/s00381-010-1241-8. Epub 2010 Aug 6.

PMID:
20694560
2.

Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patients.

Roder C, Peters V, Kasuya H, Nishizawa T, Takehara Y, Berg D, Schulte C, Khan N, Tatagiba M, Krischek B.

Acta Neurochir (Wien). 2010 Dec;152(12):2153-60. doi: 10.1007/s00701-010-0711-9. Epub 2010 Jun 23.

PMID:
20571834
3.

Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease.

Kim EH, Yum MS, Ra YS, Park JB, Ahn JS, Kim GH, Goo HW, Ko TS, Yoo HW.

J Neurosurg. 2016 May;124(5):1221-7. doi: 10.3171/2015.4.JNS142900. Epub 2015 Oct 2.

PMID:
26430847
4.

Analysis of TGFB1 in European and Japanese Moyamoya disease patients.

Liu C, Roder C, Schulte C, Kasuya H, Akagawa H, Nishizawa T, Yoneyama T, Okada Y, Khan N, Tatagiba M, Berg D, Krischek B.

Eur J Med Genet. 2012 Oct;55(10):531-4. doi: 10.1016/j.ejmg.2012.05.002. Epub 2012 Jun 1.

PMID:
22659181
5.

The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature.

Zhang Q, Liu Y, Yu L, Duan R, Ma Y, Ge P, Zhang D, Zhang Y, Wang R, Wang S, Zhao Y, Cao Y, Liu X, Deng X, Zhao J, Zhang X.

World Neurosurg. 2017 Mar;99:701-708.e1. doi: 10.1016/j.wneu.2016.12.119. Epub 2017 Jan 5. Review.

PMID:
28063898
6.

The Role of RNF213 4810G>A and 4950G>A Variants in Patients with Moyamoya Disease in Korea.

Park YS, An HJ, Kim JO, Kim WS, Han IB, Kim OJ, Kim NK, Kim DS.

Int J Mol Sci. 2017 Nov 21;18(11). pii: E2477. doi: 10.3390/ijms18112477.

7.

Impacts and interactions of PDGFRB, MMP-3, TIMP-2, and RNF213 polymorphisms on the risk of Moyamoya disease in Han Chinese human subjects.

Wang X, Zhang Z, Liu W, Xiong Y, Sun W, Huang X, Jiang Y, Ni G, Sun W, Zhou L, Wu L, Zhu W, Li H, Liu X, Xu G.

Gene. 2013 Sep 10;526(2):437-42. doi: 10.1016/j.gene.2013.05.083. Epub 2013 Jun 12.

PMID:
23769926
8.

The roles of methylenetetrahydrofolate reductase 677C>T and 1298A>C polymorphisms in moyamoya disease patients.

Park YS, Jeon YJ, Kim HS, Han IB, Choi JU, Kim DS, Kim NK.

Childs Nerv Syst. 2014 Oct;30(10):1687-95. doi: 10.1007/s00381-014-2495-3. Epub 2014 Aug 7.

PMID:
25098357
9.

Single nucleotide polymorphisms of tissue inhibitor of metalloproteinase genes in familial moyamoya disease.

Kang HS, Kim SK, Cho BK, Kim YY, Hwang YS, Wang KC.

Neurosurgery. 2006 Jun;58(6):1074-80; discussion 1074-80.

PMID:
16723886
10.

Association of the miR-146aC>G, miR-196a2C>T, and miR-499A>G polymorphisms with moyamoya disease in the Korean population.

Park YS, Jeon YJ, Lee BE, Kim TG, Choi JU, Kim DS, Kim NK.

Neurosci Lett. 2012 Jul 11;521(1):71-5. doi: 10.1016/j.neulet.2012.05.062. Epub 2012 May 30.

PMID:
22659075
11.

Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study.

Duan L, Wei L, Tian Y, Zhang Z, Hu P, Wei Q, Liu S, Zhang J, Wang Y, Li D, Yang W, Zong R, Xian P, Han C, Bao X, Zhao F, Feng J, Liu W, Cao W, Zhou G, Zhu C, Yu F, Yang W, Meng Y, Wang J, Chen X, Wang Y, Shen B, Zhao B, Wan J, Zhang F, Zhao G, Xu A, Zhang X, Liu J, Zuo X, Wang K.

Stroke. 2018 Jan;49(1):11-18. doi: 10.1161/STROKEAHA.117.017430.

PMID:
29273593
12.

Genetic and clinical characteristics of Moyamoya disease in Europeans.

Krischek B, Kasuya H, Khan N, Tatagiba M, Roder C, Kraemer M.

Acta Neurochir Suppl. 2011;112:31-4. doi: 10.1007/978-3-7091-0661-7_6.

PMID:
21691984
13.

Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing.

Shoemaker LD, Clark MJ, Patwardhan A, Chandratillake G, Garcia S, Chen R, Morgan AA, Leng N, Kirk S, Chen R, Cook DJ, Snyder M, Steinberg GK.

G3 (Bethesda). 2015 Nov 3;6(1):41-9. doi: 10.1534/g3.115.020321.

14.

Analysis of ACTA2 in European Moyamoya disease patients.

Roder C, Peters V, Kasuya H, Nishizawa T, Wakita S, Berg D, Schulte C, Khan N, Tatagiba M, Krischek B.

Eur J Paediatr Neurol. 2011 Mar;15(2):117-22. doi: 10.1016/j.ejpn.2010.09.002. Epub 2010 Oct 20.

PMID:
20970362
15.

Age-specific eNOS polymorphisms in moyamoya disease.

Park YS, Min KT, Kim TG, Lee YH, Cheong HJ, Yeom IS, Choi JU, Kim DS, Kim NK.

Childs Nerv Syst. 2011 Nov;27(11):1919-26. doi: 10.1007/s00381-011-1504-z. Epub 2011 Jun 21.

PMID:
21691823
16.

Association of a functional polymorphism in the MMP-3 gene with Moyamoya Disease in the Chinese Han population.

Li H, Zhang ZS, Liu W, Yang WZ, Dong ZN, Ma MJ, Han C, Yang H, Cao WC, Duan L.

Cerebrovasc Dis. 2010;30(6):618-25. doi: 10.1159/000319893. Epub 2010 Oct 15.

PMID:
20948207
17.

Differences in the Genotype Frequency of the RNF213 Variant in Patients with Familial Moyamoya Disease in Kyushu, Japan.

Takamatsu Y, Higashimoto K, Maeda T, Kawashima M, Matsuo M, Abe T, Matsushima T, Soejima H.

Neurol Med Chir (Tokyo). 2017 Nov 15;57(11):607-611. doi: 10.2176/nmc.oa.2017-0036. Epub 2017 Sep 21.

18.

Frequency and significance of rare RNF213 variants in patients with adult moyamoya disease.

Jang MA, Chung JW, Yeon JY, Kim JS, Hong SC, Bang OY, Ki CS.

PLoS One. 2017 Jun 15;12(6):e0179689. doi: 10.1371/journal.pone.0179689. eCollection 2017.

19.

Inheritance of moyamoya disease in a Caucasian family.

Kraemer M, Heinemann FM, Horn PA, Venker C, Berlit P, Krischek B, Khan N.

Eur J Neurol. 2012 Mar;19(3):438-42. doi: 10.1111/j.1468-1331.2011.03536.x. Epub 2011 Oct 4.

PMID:
21974719
20.

RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients.

Kobayashi H, Brozman M, Kyselová K, Viszlayová D, Morimoto T, Roubec M, Školoudík D, Petrovičová A, Juskanič D, Strauss J, Halaj M, Kurray P, Hranai M, Harada KH, Inoue S, Yoshida Y, Habu T, Herzig R, Youssefian S, Koizumi A.

PLoS One. 2016 Oct 13;11(10):e0164759. doi: 10.1371/journal.pone.0164759. eCollection 2016.

Supplemental Content

Support Center