260 related articles for article (PubMed ID: 28402226)
1. The first Greek case of heterozygous cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy: An atypical clinico-radiological presentation.
Bougea A; Velonakis G; Spantideas N; Anagnostou E; Paraskevas G; Kapaki E; Kararizou E
Neuroradiol J; 2017 Dec; 30(6):583-585. PubMed ID: 28402226
[TBL] [Abstract][Full Text] [Related]
2. [Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL)].
Uemura M; Nozaki H; Onodera O
Brain Nerve; 2017 Jan; 69(1):25-33. PubMed ID: 28126975
[TBL] [Abstract][Full Text] [Related]
3. Distinct molecular mechanisms of HTRA1 mutants in manifesting heterozygotes with CARASIL.
Nozaki H; Kato T; Nihonmatsu M; Saito Y; Mizuta I; Noda T; Koike R; Miyazaki K; Kaito M; Ito S; Makino M; Koyama A; Shiga A; Uemura M; Sekine Y; Murakami A; Moritani S; Hara K; Yokoseki A; Kuwano R; Endo N; Momotsu T; Yoshida M; Nishizawa M; Mizuno T; Onodera O
Neurology; 2016 May; 86(21):1964-74. PubMed ID: 27164673
[TBL] [Abstract][Full Text] [Related]
4. A Case of Leukoencephalopathy and Small Vessels Disease Caused by a Novel HTRA1 Homozygous Mutation.
Gündüz T; Demirkol Y; Doğan Ö; Demir S; Akçakaya NH
J Stroke Cerebrovasc Dis; 2019 Nov; 28(11):104354. PubMed ID: 31494012
[TBL] [Abstract][Full Text] [Related]
5. Heterozygous HTRA1 mutations with mimicking symptoms of CARASIL in two families.
Kono Y; Nishioka K; Li Y; Komatuzaki Y; Ito Y; Yoshino H; Tanaka R; Iguchi Y; Hattori N
Clin Neurol Neurosurg; 2018 Sep; 172():174-176. PubMed ID: 30031255
[TBL] [Abstract][Full Text] [Related]
6. A novel mutation of the high-temperature requirement A serine peptidase 1 (HTRA1) gene in a Chinese family with cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).
Chen Y; He Z; Meng S; Li L; Yang H; Zhang X
J Int Med Res; 2013 Oct; 41(5):1445-55. PubMed ID: 23963851
[TBL] [Abstract][Full Text] [Related]
7. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): A challenging diagnosis and a rare multiple sclerosis mimic.
Shirah B; Algahtani H; Algahtani R; Alfares A; Hassan A
J Stroke Cerebrovasc Dis; 2023 Aug; 32(8):107225. PubMed ID: 37348440
[TBL] [Abstract][Full Text] [Related]
8. HTRA1-related autosomal dominant cerebral small vessel disease.
Liu JY; Zhu YC; Zhou LX; Wei YP; Mao CH; Cui LY; Peng B; Yao M
Chin Med J (Engl); 2020 Oct; 134(2):178-184. PubMed ID: 33109952
[TBL] [Abstract][Full Text] [Related]
9. Characterization of Heterozygous
Lee YC; Chung CP; Chao NC; Fuh JL; Chang FC; Soong BW; Liao YC
Stroke; 2018 Jul; 49(7):1593-1601. PubMed ID: 29895533
[TBL] [Abstract][Full Text] [Related]
10. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): from discovery to gene identification.
Fukutake T
J Stroke Cerebrovasc Dis; 2011; 20(2):85-93. PubMed ID: 21215656
[TBL] [Abstract][Full Text] [Related]
11. Cerebral Small Vessel Disease Related to a Heterozygous Nonsense Mutation in HTRA1.
Ohta K; Ozawa T; Fujinaka H; Goto K; Nakajima T
Intern Med; 2020 May; 59(10):1309-1313. PubMed ID: 32101834
[TBL] [Abstract][Full Text] [Related]
12. Report of two pedigrees with heterozygous HTRA1 variants-related cerebral small vessel disease and literature review.
Zhou H; Jiao B; Ouyang Z; Wu Q; Shen L; Fang L
Mol Genet Genomic Med; 2022 Oct; 10(10):e2032. PubMed ID: 35946346
[TBL] [Abstract][Full Text] [Related]
13. Genetically Confirmed CARASIL: Case Report with Novel HTRA1 Mutation and Literature Review.
Yu Z; Cao S; Wu A; Yue H; Zhang C; Wang J; Xia M; Wu J
World Neurosurg; 2020 Nov; 143():121-128. PubMed ID: 32445900
[TBL] [Abstract][Full Text] [Related]
14. Establishment and identification of a novel HTRA1 mutation mice model.
Li C; Jin W; Wang X; Li T; Wang M; Cao B
Rev Cardiovasc Med; 2019 Sep; 20(3):179-186. PubMed ID: 31601092
[TBL] [Abstract][Full Text] [Related]
15. Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).
Tan RY; Drazyk AM; Urankar K; Bailey C; Gräf S; Markus H; Giffin NJ
Pract Neurol; 2021 Oct; 21(5):448-451. PubMed ID: 34433685
[TBL] [Abstract][Full Text] [Related]
16. Candesartan prevents arteriopathy progression in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy model.
Kato T; Manabe RI; Igarashi H; Kametani F; Hirokawa S; Sekine Y; Fujita N; Saito S; Kawashima Y; Hatano Y; Ando S; Nozaki H; Sugai A; Uemura M; Fukunaga M; Sato T; Koyama A; Saito R; Sugie A; Toyoshima Y; Kawata H; Murayama S; Matsumoto M; Kakita A; Hasegawa M; Ihara M; Kanazawa M; Nishizawa M; Tsuji S; Onodera O
J Clin Invest; 2021 Nov; 131(22):. PubMed ID: 34779414
[TBL] [Abstract][Full Text] [Related]
17. Monogenic causes of stroke: now and the future.
Tan RY; Markus HS
J Neurol; 2015 Dec; 262(12):2601-16. PubMed ID: 26037017
[TBL] [Abstract][Full Text] [Related]
18. [Consideration of the pathogenesis of CARASIL].
Nozaki H
Rinsho Shinkeigaku; 2012; 52(11):1360-2. PubMed ID: 23196618
[TBL] [Abstract][Full Text] [Related]
19. Shifting the CARASIL paradigm: report of a non-Asian family and literature review.
Menezes Cordeiro I; Nzwalo H; Sá F; Ferreira RB; Alonso I; Afonso L; Basílio C
Stroke; 2015 Apr; 46(4):1110-2. PubMed ID: 25712943
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
