These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
487 related articles for article (PubMed ID: 31699577)
1. 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]
2. 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]
3. Cerebral Microbleed Burdens in Specific Brain Regions Are Associated With Disease Severity of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy. Chung CP; Chen JW; Chang FC; Li WC; Lee YC; Chen LF; Liao YC J Am Heart Assoc; 2020 Jul; 9(13):e016233. PubMed ID: 32552418 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. Multiple Border-Zone Infarcts Triggered by Influenza A Virus Infection in a Patient With Cerebral Autosomal Dominant Arteriopathy Presenting With Subcortical Infarcts and Leukoencephalopathy. Mizutani K; Sakurai K; Mizuta I; Mizuno T; Yuasa H J Stroke Cerebrovasc Dis; 2020 May; 29(5):104701. PubMed ID: 32102741 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. Clinical and imaging features of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and cysteine-sparing NOTCH3 mutations. Kim H; Lim YM; Lee EJ; Oh YJ; Kim KK PLoS One; 2020; 15(6):e0234797. PubMed ID: 32555735 [TBL] [Abstract][Full Text] [Related]
12. Genotype-phenotype correlations of cysteine replacement in CADASIL. Matsushima T; Conedera S; Tanaka R; Li Y; Yoshino H; Funayama M; Ikeda A; Hosaka Y; Okuzumi A; Shimada Y; Yamashiro K; Motoi Y; Nishioka K; Hattori N Neurobiol Aging; 2017 Feb; 50():169.e7-169.e14. PubMed ID: 27890607 [TBL] [Abstract][Full Text] [Related]
13. Acute simultaneous multiple lacunar infarcts as the initial presentation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Hsiao CT; Chen YC; Liu YT; Soong BW; Lee YC J Chin Med Assoc; 2015 Jul; 78(7):424-6. PubMed ID: 25959358 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy without anterior temporal pole involvement: a case report. Kobayashi J; Sato S; Okumura K; Miyashita F; Ueda A; Ando Y; Toyoda K J Stroke Cerebrovasc Dis; 2014 Mar; 23(3):e241-2. PubMed ID: 24295602 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Heterozygous Cysteine-sparing NOTCH3 Variant p.Val237Met in a Japanese Patient with Suspected Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy. Kano Y; Mizuta I; Ueda A; Nozaki H; Sakurai K; Onodera O; Ando Y; Yamada K; Yuasa H; Mizuno T Intern Med; 2021 Aug; 60(15):2479-2482. PubMed ID: 33678736 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]