141 related articles for article (PubMed ID: 28782182)
1. Heterozygous mutations of HTRA1 gene in patients with familial cerebral small vessel disease.
Di Donato I; Bianchi S; Gallus GN; Cerase A; Taglia I; Pescini F; Nannucci S; Battisti C; Inzitari D; Pantoni L; Zini A; Federico A; Dotti MT
CNS Neurosci Ther; 2017 Sep; 23(9):759-765. PubMed ID: 28782182
[TBL] [Abstract][Full Text] [Related]
2. Association of
Cerfontaine MN; Hack RJ; Gesierich B; Duering M; Witjes-Ané MW; Rodríguez-Girondo M; Gravesteijn G; Rutten J; Lesnik Oberstein SAJ
Neurology; 2024 May; 102(10):e209310. PubMed ID: 38713890
[TBL] [Abstract][Full Text] [Related]
3. Pathophysiology of cerebral small vessel disease: a journey through recent discoveries.
Dupré N; Drieu A; Joutel A
J Clin Invest; 2024 May; 134(10):. PubMed ID: 38747292
[TBL] [Abstract][Full Text] [Related]
4. Microbleeds in Heterozygous HTRA1-Related Cerebral Small Vessel Disease.
Guo Y; Peng Q; Ling C
JAMA Neurol; 2024 May; 81(5):551-552. PubMed ID: 38466301
[TBL] [Abstract][Full Text] [Related]
5. Dysfunctional effort-based decision-making underlies apathy in genetic cerebral small vessel disease.
Le Heron C; Manohar S; Plant O; Muhammed K; Griffanti L; Nemeth A; Douaud G; Markus HS; Husain M
Brain; 2018 Nov; 141(11):3193-3210. PubMed ID: 30346491
[TBL] [Abstract][Full Text] [Related]
6. Rs2293871 regulates HTRA1 expression and affects cerebral small vessel stroke and Alzheimer's disease.
Liu G; Zhang H; Liu B; Ji X
Brain; 2019 Nov; 142(11):e61. PubMed ID: 31603204
[No Abstract] [Full Text] [Related]
7. Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3.
Sassi C; Nalls MA; Ridge PG; Gibbs JR; Lupton MK; Troakes C; Lunnon K; Al-Sarraj S; Brown KS; Medway C; Lord J; Turton J; Bras J; ; Blumenau S; Thielke M; Josties C; Freyer D; Dietrich A; Hammer M; Baier M; Dirnagl U; Morgan K; Powell JF; Kauwe JS; Cruchaga C; Goate AM; Singleton AB; Guerreiro R; Hodges A; Hardy J
Neurobiol Aging; 2018 Jun; 66():179.e17-179.e29. PubMed ID: 29544907
[TBL] [Abstract][Full Text] [Related]
8. Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensities.
Malik R; Beaufort N; Frerich S; Gesierich B; Georgakis MK; Rannikmäe K; Ferguson AC; Haffner C; Traylor M; Ehrmann M; Sudlow CLM; Dichgans M
Brain; 2021 Oct; 144(9):2670-2682. PubMed ID: 34626176
[TBL] [Abstract][Full Text] [Related]
9. Cerebrovascular disorders associated with genetic lesions.
Karschnia P; Nishimura S; Louvi A
Cell Mol Life Sci; 2019 Jan; 76(2):283-300. PubMed ID: 30327838
[TBL] [Abstract][Full Text] [Related]
10. Sex Differences in Cerebral Small Vessel Disease: A Systematic Review and Meta-Analysis.
Jiménez-Sánchez L; Hamilton OKL; Clancy U; Backhouse EV; Stewart CR; Stringer MS; Doubal FN; Wardlaw JM
Front Neurol; 2021; 12():756887. PubMed ID: 34777227
[No Abstract] [Full Text] [Related]
11. A CARASIL patient with a novel HTRA1 mutation accompanied by macular cystic edema: A case report and literature review.
Zhai N; Hu J; Yan H
Asian J Surg; 2024 Jun; ():. PubMed ID: 38879362
[No Abstract] [Full Text] [Related]
12. Systematic Review of Cysteine-Sparing NOTCH3 Missense Mutations in Patients with Clinical Suspicion of CADASIL.
Muiño E; Gallego-Fabrega C; Cullell N; Carrera C; Torres N; Krupinski J; Roquer J; Montaner J; Fernández-Cadenas I
Int J Mol Sci; 2017 Sep; 18(9):. PubMed ID: 28902129
[TBL] [Abstract][Full Text] [Related]
13. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.
Joutel A; Corpechot C; Ducros A; Vahedi K; Chabriat H; Mouton P; Alamowitch S; Domenga V; Cécillion M; Marechal E; Maciazek J; Vayssiere C; Cruaud C; Cabanis EA; Ruchoux MM; Weissenbach J; Bach JF; Bousser MG; Tournier-Lasserve E
Nature; 1996 Oct; 383(6602):707-10. PubMed ID: 8878478
[TBL] [Abstract][Full Text] [Related]
14. New diagnostic criteria for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukocencephalopathy in Japan.
Mizuta I; Watanabe-Hosomi A; Koizumi T; Mukai M; Hamano A; Tomii Y; Kondo M; Nakagawa M; Tomimoto H; Hirano T; Uchino M; Onodera O; Mizuno T
J Neurol Sci; 2017 Oct; 381():62-67. PubMed ID: 28991717
[TBL] [Abstract][Full Text] [Related]
15. Cerebral Microbleeds and the Risk of Incident Ischemic Stroke in CADASIL (Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy).
Puy L; De Guio F; Godin O; Duering M; Dichgans M; Chabriat H; Jouvent E
Stroke; 2017 Oct; 48(10):2699-2703. PubMed ID: 28842512
[TBL] [Abstract][Full Text] [Related]
16. A prospective multicenter study on genome wide associations to ranibizumab treatment outcome for age-related macular degeneration.
Yamashiro K; Mori K; Honda S; Kano M; Yanagi Y; Obana A; Sakurada Y; Sato T; Nagai Y; Hikichi T; Kataoka Y; Hara C; Koyama Y; Koizumi H; Yoshikawa M; Miyake M; Nakata I; Tsuchihashi T; Horie-Inoue K; Matsumiya W; Ogasawara M; Obata R; Yoneyama S; Matsumoto H; Ohnaka M; Kitamei H; Sayanagi K; Ooto S; Tamura H; Oishi A; Kabasawa S; Ueyama K; Miki A; Kondo N; Bessho H; Saito M; Takahashi H; Tan X; Azuma K; Kikushima W; Mukai R; Ohira A; Gomi F; Miyata K; Takahashi K; Kishi S; Iijima H; Sekiryu T; Iida T; Awata T; Inoue S; Yamada R; Matsuda F; Tsujikawa A; Negi A; Yoneya S; Iwata T; Yoshimura N
Sci Rep; 2017 Aug; 7(1):9196. PubMed ID: 28835685
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. CADASIL brain vessels show a HTRA1 loss-of-function profile.
Zellner A; Scharrer E; Arzberger T; Oka C; Domenga-Denier V; Joutel A; Lichtenthaler SF; Müller SA; Dichgans M; Haffner C
Acta Neuropathol; 2018 Jul; 136(1):111-125. PubMed ID: 29725820
[TBL] [Abstract][Full Text] [Related]
19.
Uemura M; Nozaki H; Kato T; Koyama A; Sakai N; Ando S; Kanazawa M; Hishikawa N; Nishimoto Y; Polavarapu K; Nalini A; Hanazono A; Kuzume D; Shindo A; El-Ghanem M; Abe A; Sato A; Yoshida M; Ikeuchi T; Mizuta I; Mizuno T; Onodera O
Front Neurol; 2020; 11():545. PubMed ID: 32719647
[TBL] [Abstract][Full Text] [Related]
20. HTRA1 expression profile and activity on TGF-β signaling in HTRA1 mutation carriers.
Fasano A; Formichi P; Taglia I; Bianchi S; Di Donato I; Battisti C; Federico A; Dotti MT
J Cell Physiol; 2020 Oct; 235(10):7120-7127. PubMed ID: 32017060
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]