190 related articles for article (PubMed ID: 34119749)
21. First report of a pathogenic mutation on exon 24 of the NOTCH3 gene in a CADASIL family.
Valenti R; Bianchi S; Pescini F; D'Eramo C; Inzitari D; Dotti MT; Pantoni L
J Neurol; 2011 Sep; 258(9):1632-6. PubMed ID: 21409506
[TBL] [Abstract][Full Text] [Related]
22. Recognition of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) in Two Oligosymptomatic Sisters with Low CADASIL Scale Scores and a Venous Dysplasia: Report of a Novel Greek Family.
Paraskevas GP; Constantinides VC; Yapijakis C; Kararizou E; Kapaki EN; Bougea A
J Stroke Cerebrovasc Dis; 2018 Sep; 27(9):e191-e195. PubMed ID: 29706439
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. [Identification of a novel NOTCH3 mutation in a family featuring cerebral autosomal dominant arteriopathy with subcortical infarct and leucoencephalopathy].
Zhu Y; Wang J; Wu Y; Wang G; Hu B; Xu A
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):578-81. PubMed ID: 25297585
[TBL] [Abstract][Full Text] [Related]
25. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: Phenotypic and mutational spectrum in patients from mainland China.
Yin X; Wu D; Wan J; Yan S; Lou M; Zhao G; Zhang B
Int J Neurosci; 2015; 125(8):585-92. PubMed ID: 25105908
[TBL] [Abstract][Full Text] [Related]
26. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese.
Lee YC; Yang AH; Liu HC; Wong WJ; Lu YC; Chang MH; Soong BW
J Neurol Sci; 2006 Jul; 246(1-2):111-5. PubMed ID: 16580020
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. 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]
30. CADASIL with a novel mutation in exon 7 of NOTCH3 (C388Y).
Ishida C; Sakajiri K; Yoshita M; Joutel A; Cave-Riant F; Yamada M
Intern Med; 2006; 45(16):981-5. PubMed ID: 16974063
[TBL] [Abstract][Full Text] [Related]
31. CADASIL and autoimmunity: coexistence in a family with the R169C mutation at exon 4 of the NOTCH3 gene.
Paraskevas GP; Bougea A; Synetou M; Vassilopoulou S; Anagnostou E; Voumvourakis K; Iliopoulos A; Spengos K
Cerebrovasc Dis; 2014; 38(4):302-7. PubMed ID: 25412914
[TBL] [Abstract][Full Text] [Related]
32. [NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
Wang ZX; Lu H; Zhang Y; Bu DF; Niu XY; Zhang Z; Huang YN; Yuan Y
Zhonghua Yi Xue Za Zhi; 2004 Jul; 84(14):1175-80. PubMed ID: 15387979
[TBL] [Abstract][Full Text] [Related]
33. CADASIL with cord involvement associated with a novel and atypical NOTCH3 mutation.
Bentley P; Wang T; Malik O; Nicholas R; Ban M; Sawcer S; Sharma P
J Neurol Neurosurg Psychiatry; 2011 Aug; 82(8):855-60. PubMed ID: 21217157
[TBL] [Abstract][Full Text] [Related]
34. Not Described Variant of Notch3 Gen for Cadasil Disease.
Mellinger S; Romero D; Visich A; Chanampa S; Ivetich G; Burgos M; Orzuza G
J Stroke Cerebrovasc Dis; 2020 Jul; 29(7):104803. PubMed ID: 32387185
[TBL] [Abstract][Full Text] [Related]
35. A novel cysteine-sparing G73A mutation of NOTCH3 in a Chinese CADASIL family.
Huang L; Li W; Li Y; Song C; Wang P; Wang H; Sun X
Neurogenetics; 2020 Jan; 21(1):39-49. PubMed ID: 31720972
[TBL] [Abstract][Full Text] [Related]
36. [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]
37. 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]
38. 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]
39. Identification of a known mutation in Notch 3 in familiar CADASIL in China.
Tan ZX; Li FF; Qu YY; Liu J; Liu GR; Zhou J; Zhu YL; Liu SL
PLoS One; 2012; 7(5):e36590. PubMed ID: 22623959
[TBL] [Abstract][Full Text] [Related]
40. Genotypic and Phenotypic Characteristics of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy from China.
Zhang C; Li S; Li W; Niu S; Wang X; Zhang Z
Eur Neurol; 2021; 84(4):237-245. PubMed ID: 34004599
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
