212 related articles for article (PubMed ID: 32387185)
1. 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]
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. 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]
4. 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]
5. 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]
6. NOTCH3 Gene Mutation in a Chilean Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Family.
Gallardo A; Latapiat V; Rivera A; Fonseca B; Roldan A; Sandoval P; Sánchez C; Matamala JM
J Stroke Cerebrovasc Dis; 2020 Feb; 29(2):104530. PubMed ID: 31813735
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. Novel mutation of the NOTCH3 gene in a Polish family with CADASIL.
Buczek J; Błażejewska-Hyżorek B; Cudna A; Lusawa M; Lewandowska E; Kurkowska-Jastrzębska I; Członkowska A
Neurol Neurochir Pol; 2016; 50(4):262-4. PubMed ID: 27375140
[TBL] [Abstract][Full Text] [Related]
11. CADASIL with a novel NOTCH3 mutation (Cys478Tyr).
Ozaki K; Irioka T; Ishikawa K; Mizusawa H
J Stroke Cerebrovasc Dis; 2015 Mar; 24(3):e61-2. PubMed ID: 25595846
[TBL] [Abstract][Full Text] [Related]
12. A novel frameshift variant in the CADASIL gene NOTCH3: pathogenic or not?
Schubert V; Bender B; Kinzel M; Peters N; Freilinger T
J Neurol; 2018 Jun; 265(6):1338-1342. PubMed ID: 29600389
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy with a Novel NOTCH3 Cys323Trp Mutation Presenting Border-Zone Infarcts: A Case Report and Literature Review.
Tojima M; Saito S; Yamamoto Y; Mizuno T; Ihara M; Fukuda H
J Stroke Cerebrovasc Dis; 2016 Aug; 25(8):e128-30. PubMed ID: 27241575
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. Unusual clinical presentations in subjects carrying novel NOTCH3 gene mutations.
Spinicci G; Conti M; Cherchi MV; Mancosu C; Murru R; Carboni N
J Stroke Cerebrovasc Dis; 2013 May; 22(4):539-44. PubMed ID: 23465844
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
