210 related articles for article (PubMed ID: 30671466)
1. RNF213 Variant Diversity Predisposes Distinct Populations to Dissimilar Cerebrovascular Diseases.
Lin J; Sheng W
Biomed Res Int; 2018; 2018():6359174. PubMed ID: 30671466
[TBL] [Abstract][Full Text] [Related]
2. Rare variants of RNF213 and moyamoya/non-moyamoya intracranial artery stenosis/occlusion disease risk: a meta-analysis and systematic review.
Liao X; Deng J; Dai W; Zhang T; Yan J
Environ Health Prev Med; 2017 Nov; 22(1):75. PubMed ID: 29165161
[TBL] [Abstract][Full Text] [Related]
3. The Clinical and Vascular Characteristics of RNF213 c.14576G>A Variant-Related Intracranial Major Artery Disease in China.
Cheng W; Xue S; Wu F; Song X; Huang Q; Song H; Wu J
Behav Neurol; 2019; 2019():7908392. PubMed ID: 30992731
[TBL] [Abstract][Full Text] [Related]
4. RNF213 p.R4810K Polymorphism and the Risk of Moyamoya Disease, Intracranial Major Artery Stenosis/Occlusion, and Quasi-Moyamoya Disease: A Meta-Analysis.
Wang Y; Mambiya M; Li Q; Yang L; Jia H; Han Y; Liu W
J Stroke Cerebrovasc Dis; 2018 Aug; 27(8):2259-2270. PubMed ID: 29752070
[TBL] [Abstract][Full Text] [Related]
5. Identification of a genetic variant common to moyamoya disease and intracranial major artery stenosis/occlusion.
Miyawaki S; Imai H; Takayanagi S; Mukasa A; Nakatomi H; Saito N
Stroke; 2012 Dec; 43(12):3371-4. PubMed ID: 23010677
[TBL] [Abstract][Full Text] [Related]
6. Genetic variant RNF213 c.14576G>A in various phenotypes of intracranial major artery stenosis/occlusion.
Miyawaki S; Imai H; Shimizu M; Yagi S; Ono H; Mukasa A; Nakatomi H; Shimizu T; Saito N
Stroke; 2013 Oct; 44(10):2894-7. PubMed ID: 23970789
[TBL] [Abstract][Full Text] [Related]
7. Role of Ring Finger Protein 213 in Moyamoya Disease.
Ma YG; Zhang Q; Yu LB; Zhao JZ
Chin Med J (Engl); 2016 Oct; 129(20):2497-2501. PubMed ID: 27748344
[TBL] [Abstract][Full Text] [Related]
8. Distribution of Intracranial Major Artery Stenosis/Occlusion According to RNF213 Polymorphisms.
Kim J; Park YS; Woo MH; An HJ; Kim JO; Park HS; Ryu CS; Kim OJ; Kim NK
Int J Mol Sci; 2020 Mar; 21(6):. PubMed ID: 32182997
[TBL] [Abstract][Full Text] [Related]
9. Moyamoya Disease and Spectrums of RNF213 Vasculopathy.
Bang OY; Chung JW; Kim DH; Won HH; Yeon JY; Ki CS; Shin HJ; Kim JS; Hong SC; Kim DK; Koizumi A
Transl Stroke Res; 2020 Aug; 11(4):580-589. PubMed ID: 31650369
[TBL] [Abstract][Full Text] [Related]
10. Genetic analysis of
Tashiro R; Fujimura M; Sakata H; Endo H; Tomata Y; Sato-Maeda M; Niizuma K; Tominaga T
Neurol Res; 2019 Sep; 41(9):811-816. PubMed ID: 31064275
[No Abstract] [Full Text] [Related]
11. Development of atherosclerotic-moyamoya syndrome with genetic variant of RNF213 p.R4810K and p.T1727M: A case report.
Liu Y; Wu X; Fan Z; Cheng J; Zhong L; Lin Y; Qu X
Clin Neurol Neurosurg; 2018 May; 168():163-166. PubMed ID: 29567577
[TBL] [Abstract][Full Text] [Related]
12. Prevalence of RNF213 variants in symptomatic intracranial arterial stenosis/occlusion in China.
Sun X; Luo M; Li J; Lai R; Lin J; Wang Y; Xu X; Wu S; Sheng W
Mol Genet Genomics; 2020 May; 295(3):635-643. PubMed ID: 32020275
[TBL] [Abstract][Full Text] [Related]
13. Genetic Analysis of RNF213 c.14576G>A Variant in Nonatherosclerotic Quasi-Moyamoya Disease.
Miyawaki S; Imai H; Shimizu M; Yagi S; Ono H; Nakatomi H; Shimizu T; Saito N
J Stroke Cerebrovasc Dis; 2015 May; 24(5):1075-9. PubMed ID: 25817623
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 26430847
[TBL] [Abstract][Full Text] [Related]
15. RNF213 rare variants in an ethnically diverse population with Moyamoya disease.
Cecchi AC; Guo D; Ren Z; Flynn K; Santos-Cortez RL; Leal SM; Wang GT; Regalado ES; Steinberg GK; Shendure J; Bamshad MJ; ; Grotta JC; Nickerson DA; Pannu H; Milewicz DM
Stroke; 2014 Nov; 45(11):3200-7. PubMed ID: 25278557
[TBL] [Abstract][Full Text] [Related]
16. Clinical characteristics and intracranial arterial lesions of non-young adult ischemic stroke patients with RNF213 p.R4810K variant.
Ogura S; Ohara T; Tanaka E; Ashida S; Maezono-Kandori K; Hanya M; Mizuta I; Mizuno T
J Neurol Sci; 2023 Sep; 452():120775. PubMed ID: 37657303
[TBL] [Abstract][Full Text] [Related]
17. Genetic Analysis of Ring Finger Protein 213 (RNF213) c.14576G>A in Intracranial Atherosclerosis of the Anterior and Posterior Circulations.
Shinya Y; Miyawaki S; Imai H; Hongo H; Ono H; Takenobu A; Nakatomi H; Teraoka A; Saito N
J Stroke Cerebrovasc Dis; 2017 Nov; 26(11):2638-2644. PubMed ID: 28797616
[TBL] [Abstract][Full Text] [Related]
18. A Polymorphism in RNF213 Is a Susceptibility Gene for Intracranial Atherosclerosis.
Bang OY; Chung JW; Cha J; Lee MJ; Yeon JY; Ki CS; Jeon P; Kim JS; Hong SC
PLoS One; 2016; 11(6):e0156607. PubMed ID: 27253870
[TBL] [Abstract][Full Text] [Related]
19. A new horizon of moyamoya disease and associated health risks explored through RNF213.
Koizumi A; Kobayashi H; Hitomi T; Harada KH; Habu T; Youssefian S
Environ Health Prev Med; 2016 Mar; 21(2):55-70. PubMed ID: 26662949
[TBL] [Abstract][Full Text] [Related]
20. RNF213 rs112735431 polymorphism in intracranial artery steno-occlusive disease and moyamoya disease in Koreans.
Park MG; Shin JH; Lee SW; Park HR; Park KP
J Neurol Sci; 2017 Apr; 375():331-334. PubMed ID: 28320162
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
