220 related articles for article (PubMed ID: 34741685)
1. Mutation spectrum and genotype-phenotype correlations in 157 Korean CADASIL patients: a multicenter study.
Min JY; Park SJ; Kang EJ; Hwang SY; Han SH
Neurogenetics; 2022 Jan; 23(1):45-58. PubMed ID: 34741685
[TBL] [Abstract][Full Text] [Related]
2. Spectrum of NOTCH3 mutations in Korean patients with clinically suspicious cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Kim YE; Yoon CW; Seo SW; Ki CS; Kim YB; Kim JW; Bang OY; Lee KH; Kim GM; Chung CS; Na DL
Neurobiol Aging; 2014 Mar; 35(3):726.e1-6. PubMed ID: 24139282
[TBL] [Abstract][Full Text] [Related]
3. Genotype-phenotype correlations and effect of mutation location in Japanese CADASIL patients.
Mukai M; Mizuta I; Watanabe-Hosomi A; Koizumi T; Matsuura J; Hamano A; Tomimoto H; Mizuno T
J Hum Genet; 2020 Aug; 65(8):637-646. PubMed ID: 32277177
[TBL] [Abstract][Full Text] [Related]
4. Novel Characteristics of Race-Specific Genetic Functions in Korean CADASIL.
Kim Y; Lee SH
Medicina (Kaunas); 2019 Aug; 55(9):. PubMed ID: 31443546
[No Abstract] [Full Text] [Related]
5. Screening for NOTCH3 gene mutations among 151 consecutive Korean patients with acute ischemic stroke.
Choi JC; Lee KH; Song SK; Lee JS; Kang SY; Kang JH
J Stroke Cerebrovasc Dis; 2013 Jul; 22(5):608-14. PubMed ID: 22133740
[TBL] [Abstract][Full Text] [Related]
6. Diversity of stroke presentation in CADASIL: study from patients harboring the predominant NOTCH3 mutation R544C.
Choi JC; Song SK; Lee JS; Kang SY; Kang JH
J Stroke Cerebrovasc Dis; 2013 Feb; 22(2):126-31. PubMed ID: 21852154
[TBL] [Abstract][Full Text] [Related]
7. Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations.
Ni W; Zhang Y; Zhang L; Xie JJ; Li HF; Wu ZY
CNS Neurosci Ther; 2022 Nov; 28(11):1779-1789. PubMed ID: 35822697
[TBL] [Abstract][Full Text] [Related]
8. Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese.
Lee YC; Liu CS; Chang MH; Lin KP; Fuh JL; Lu YC; Liu YF; Soong BW
J Neurol; 2009 Feb; 256(2):249-55. PubMed ID: 19242647
[TBL] [Abstract][Full Text] [Related]
9. Clinical features and mutation spectrum in Chinese patients with CADASIL: A multicenter retrospective study.
Chen S; Ni W; Yin XZ; Liu HQ; Lu C; Zheng QJ; Zhao GX; Xu YF; Wu L; Zhang L; Wang N; Li HF; Wu ZY
CNS Neurosci Ther; 2017 Sep; 23(9):707-716. PubMed ID: 28710804
[TBL] [Abstract][Full Text] [Related]
10. Genotype and Phenotype Differences in CADASIL from an Asian Perspective.
Kim Y; Bae JS; Lee JY; Song HK; Lee JH; Lee M; Kim C; Lee SH
Int J Mol Sci; 2022 Sep; 23(19):. PubMed ID: 36232798
[TBL] [Abstract][Full Text] [Related]
11. A Chinese CADASIL Family with a Novel Mutation on Exon 10 of Notch3 Gene.
Liu Y; Huang S; Yu L; Li T; Diao S; Chen Z; Zhou G; Sheng X; Xu Y; Fang Q
J Stroke Cerebrovasc Dis; 2021 Aug; 30(8):105674. PubMed ID: 34119749
[TBL] [Abstract][Full Text] [Related]
12.
Lee YC; Chung CP; Chang MH; Wang SJ; Liao YC
Neurology; 2020 Jan; 94(1):e87-e96. PubMed ID: 31792094
[TBL] [Abstract][Full Text] [Related]
13. Imaging-based pregenetic screening for NOTCH3 p.R544C mutation in ischemic stroke in Taiwan.
Cheng YW; Chen CH; Hu CJ; Chiou HY; Tang SC; Jeng JS
Ann Clin Transl Neurol; 2020 Oct; 7(10):1951-1961. PubMed ID: 32929895
[TBL] [Abstract][Full Text] [Related]
14. A Japanese Case of CADASIL with a Rare Mutation in Exon 24 of the NOTCH3 Gene.
Ebihara Y; Mochizuki H; Ishii N; Mizuta I; Shiomi K; Mizuno T; Nakazato M
Intern Med; 2018 Oct; 57(20):3011-3014. PubMed ID: 29780132
[TBL] [Abstract][Full Text] [Related]
15. Characteristics of CADASIL in Korea: a novel cysteine-sparing Notch3 mutation.
Kim Y; Choi EJ; Choi CG; Kim G; Choi JH; Yoo HW; Kim JS
Neurology; 2006 May; 66(10):1511-6. PubMed ID: 16717210
[TBL] [Abstract][Full Text] [Related]
16. Novel heterozygous NOTCH3 pathogenic variant found in two Chinese patients with CADASIL.
Li S; Chen Y; Shan H; Ma F; Shi M; Xue J
J Clin Neurosci; 2017 Dec; 46():85-89. PubMed ID: 28867359
[TBL] [Abstract][Full Text] [Related]
17. Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles.
Liao YC; Hsiao CT; Fuh JL; Chern CM; Lee WJ; Guo YC; Wang SJ; Lee IH; Liu YT; Wang YF; Chang FC; Chang MH; Soong BW; Lee YC
PLoS One; 2015; 10(8):e0136501. PubMed ID: 26308724
[TBL] [Abstract][Full Text] [Related]
18. Broad phenotype of cysteine-altering
Rutten JW; Hack RJ; Duering M; Gravesteijn G; Dauwerse JG; Overzier M; van den Akker EB; Slagboom E; Holstege H; Nho K; Saykin A; Dichgans M; Malik R; Lesnik Oberstein SAJ
Neurology; 2020 Sep; 95(13):e1835-e1843. PubMed ID: 32732295
[TBL] [Abstract][Full Text] [Related]
19. A Novel Mutation Outside of the EGFr Encoding Exons of NOTCH3 Gene in a Chinese with CADASIL.
Wang W; Ren Z; Shi Y; Zhang J
J Stroke Cerebrovasc Dis; 2020 Dec; 29(12):105410. PubMed ID: 33254371
[TBL] [Abstract][Full Text] [Related]
20. NOTCH3 mutations in a cohort of Portuguese patients within CADASIL spectrum phenotype.
Almeida MR; Elias I; Fernandes C; Machado R; Galego O; Santo G
Neurogenetics; 2022 Jan; 23(1):1-9. PubMed ID: 34851492
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
