195 related articles for article (PubMed ID: 34352628)
1. A Chinese CADASIL family with p.R578C mutation at exon 11 of the NOTCH3 gene.
Wu X; Zhang A; Li Y; Lei X; Guo S; Tian T; Gong H; He D
Clin Neurol Neurosurg; 2021 Sep; 208():106833. PubMed ID: 34352628
[TBL] [Abstract][Full Text] [Related]
2. A Novel Heterozygous Variant in Exon 19 of NOTCH3 in a Saudi Family with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy.
Algahtani H; Shirah B; Alharbi SY; Al-Qahtani MH; Abdulkareem AA; Naseer MI
J Stroke Cerebrovasc Dis; 2020 Jul; 29(7):104832. PubMed ID: 32414585
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. First Report of Arg587Cys Mutation of Notch3 Gene in Two Chinese Families with CADASIL.
You J; Liao S; Zhang F; Ma Z; Li G
J Stroke Cerebrovasc Dis; 2017 Jan; 26(1):e1-e4. PubMed ID: 28341077
[TBL] [Abstract][Full Text] [Related]
6. Novel Mutation of the NOTCH3 Gene in a Chinese Pedigree with CADASIL.
Hou X; He C; Jin Q; Niu Q; Ren G; Cheng H
CNS Neurol Disord Drug Targets; 2017; 16(1):30-35. PubMed ID: 27781952
[TBL] [Abstract][Full Text] [Related]
7. 3T MRI study discloses high intrafamilial variability in CADASIL due to a novel NOTCH3 mutation.
La Piana R; Leppert IR; Pike GB; Lanthier S; Brais B; Tampieri D
J Clin Neurosci; 2018 Dec; 58():25-29. PubMed ID: 30454692
[TBL] [Abstract][Full Text] [Related]
8. [NOTCH3 gene mutations in two Chinese families featuring cerebral autosomal dominant arteriopathy with subcortical infarct and leucoencephalopathy].
Sun Q; Li W; Zhou Y; Yi F; Wang J; Hu Y; Yao L; Zhou L; Xu H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):816-820. PubMed ID: 29188607
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Novel and Recurring NOTCH3 Mutations in Two Chinese Patients with CADASIL.
Chen X; Deng S; Xu H; Hou D; Hu P; Yang Y; Wen J; Deng H; Yuan L
Neurodegener Dis; 2019; 19(1):35-42. PubMed ID: 31212292
[TBL] [Abstract][Full Text] [Related]
11. Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family.
Abou Al-Shaar H; Qadi N; Al-Hamed MH; Meyer BF; Bohlega S
J Neurol Sci; 2016 Aug; 367():239-43. PubMed ID: 27423596
[TBL] [Abstract][Full Text] [Related]
12. A novel report of Cys1298Gly mutation in exon 24 of NOTCH3 gene in a Chinese family with CADASIL.
Hu J; Qian J; Che Z; Tang B; Li Y; Gong Q; Lu X
J Stroke Cerebrovasc Dis; 2023 Aug; 32(8):107208. PubMed ID: 37295172
[TBL] [Abstract][Full Text] [Related]
13. Clinical Features of 4 Novel NOTCH3 Mutations of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy in China.
Qin W; Ren Z; Xia M; Yang M; Shi Y; Huang Y; Guo X; Zhang J
Med Sci Monit Basic Res; 2019 Sep; 25():199-209. PubMed ID: 31554780
[TBL] [Abstract][Full Text] [Related]
14. Homozygous NOTCH3 p.R587C mutation in Chinese patients with CADASIL: a case report.
He R; Li H; Sun Y; Chen M; Wang L; Zhu Y; Zhang C
BMC Neurol; 2020 Mar; 20(1):72. PubMed ID: 32122318
[TBL] [Abstract][Full Text] [Related]
15. What factors determine phenotype of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)? Considerations in the context of a novel pathogenic R110C mutation in the NOTCH3 gene.
Dziewulska D; Sulejczak D; Wężyk M
Folia Neuropathol; 2017; 55(4):295-300. PubMed ID: 29363903
[No Abstract] [Full Text] [Related]
16. 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]
17. A Novel NOTCH3 Gene Mutation in a Polish CADASIL Family.
Machowska-Sempruch K; Bajer-Czajkowska A; Makarewicz K; Zaryczańska K; Koryzma A; Nowacki P
J Stroke Cerebrovasc Dis; 2019 Mar; 28(3):574-576. PubMed ID: 30545719
[TBL] [Abstract][Full Text] [Related]
18. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) associated with a novel C82R mutation in the NOTCH3 gene.
Zea-Sevilla MA; Bermejo-Velasco P; Serrano-Heranz R; Calero M
J Alzheimers Dis; 2015; 43(2):363-7. PubMed ID: 25096610
[TBL] [Abstract][Full Text] [Related]
19. Clinical presentation of Y189C mutation of the NOTCH3 gene in the Polish family with CADASIL.
Dorszewska J; Kowalska M; Grzegorski T; Dziewulska D; Karmelita-Katulska K; Barciszewska AM; Prendecki M; Gorczyński W; Kozubski W
Folia Neuropathol; 2020; 58(1):83-92. PubMed ID: 32337960
[TBL] [Abstract][Full Text] [Related]
20. Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Associated With a Novel In-Frame Mutation in the NOTCH3 Gene in a Japanese Patient.
Takeshi Y; Suda S; Shimoyama T; Aoki J; Suzuki K; Okubo S; Mizuta I; Mizuno T; Kimura K
J Stroke Cerebrovasc Dis; 2020 Jan; 29(1):104482. PubMed ID: 31699577
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
