239 related articles for article (PubMed ID: 23963851)
41. [Consideration of the pathogenesis of CARASIL].
Nozaki H
Rinsho Shinkeigaku; 2012; 52(11):1360-2. PubMed ID: 23196618
[TBL] [Abstract][Full Text] [Related]
42. HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF-β/Smad signaling pathway in CARASIL model mice.
Chuanfen L; Xiaoling W; Wen J; Bingzhen C; Min W
Brain Behav; 2022 Aug; 12(8):e2691. PubMed ID: 35841197
[TBL] [Abstract][Full Text] [Related]
43. Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy.
Pippucci T; Maresca A; Magini P; Cenacchi G; Donadio V; Palombo F; Papa V; Incensi A; Gasparre G; Valentino ML; Preziuso C; Pisano A; Ragno M; Liguori R; Giordano C; Tonon C; Lodi R; Parmeggiani A; Carelli V; Seri M
EMBO Mol Med; 2015 Jun; 7(6):848-58. PubMed ID: 25870235
[TBL] [Abstract][Full Text] [Related]
44. [Molecular pathogenesis of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy].
Shiga A; Nozaki H; Nishizawa M; Onodera O
Brain Nerve; 2010 Jun; 62(6):595-9. PubMed ID: 20548119
[TBL] [Abstract][Full Text] [Related]
45. Histopathologic features of an autopsied patient with cerebral small vessel disease and a heterozygous HTRA1 mutation.
Ito J; Nozaki H; Toyoshima Y; Abe T; Sato A; Hashidate H; Igarashi S; Onodera O; Takahashi H; Kakita A
Neuropathology; 2018 May; ():. PubMed ID: 29797751
[TBL] [Abstract][Full Text] [Related]
46. [Clinical manifestations and neuroradiological findings of CARASIL with a novel mutation].
Shibata M
Rinsho Shinkeigaku; 2012; 52(11):1363-4. PubMed ID: 23196619
[TBL] [Abstract][Full Text] [Related]
47.
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]
48. Case Report: Diffuse Cerebral Microbleeds in Cerebral Autosomal Recessive Arteriopathy With Subcortical Infarcts and Leukoencephalopathy.
Wen L; Yuan J; Li S; Zhao J; Li C; Li J; Han Y; Wang C; Li G
Front Neurol; 2022; 13():818332. PubMed ID: 35222251
[TBL] [Abstract][Full Text] [Related]
49. [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]
50. Characteristic features and progression of abnormalities on MRI for CARASIL.
Nozaki H; Sekine Y; Fukutake T; Nishimoto Y; Shimoe Y; Shirata A; Yanagawa S; Hirayama M; Tamura M; Nishizawa M; Onodera O
Neurology; 2015 Aug; 85(5):459-63. PubMed ID: 26138950
[TBL] [Abstract][Full Text] [Related]
51. Histopathologic Analysis of Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CARASIL): A Report of a New Genetically Confirmed Case and Comparison to 2 Previous Cases.
Ito S; Takao M; Fukutake T; Hatsuta H; Funabe S; Ito N; Shimoe Y; Niki T; Nakano I; Fukayama M; Murayama S
J Neuropathol Exp Neurol; 2016 Nov; 75(11):1020-1030. PubMed ID: 27634960
[TBL] [Abstract][Full Text] [Related]
52. Heterozygous
Yao T; Zhu J; Wu X; Li X; Fu Y; Wang Y; Wang Z; Xu F; Lai H; He A; Teng L; Wang C; Song H
Neurol Genet; 2022 Dec; 8(6):e200044. PubMed ID: 36524103
[TBL] [Abstract][Full Text] [Related]
53. Identified novel heterozygous
Chen MJ; Zhang Y; Luo WJ; Dong HL; Wei Q; Zhang J; Ruan QQ; Ni W; Li HF
Front Genet; 2022; 13():909131. PubMed ID: 36035189
[No Abstract] [Full Text] [Related]
54. A novel mutation in the HTRA1 gene causes CARASIL without alopecia.
Nishimoto Y; Shibata M; Nihonmatsu M; Nozaki H; Shiga A; Shirata A; Yamane K; Kosakai A; Takahashi K; Nishizawa M; Onodera O; Suzuki N
Neurology; 2011 Apr; 76(15):1353-5. PubMed ID: 21482952
[No Abstract] [Full Text] [Related]
55. Loss of HtrA1-induced attenuation of TGF-β signaling in fibroblasts might not be the main mechanism of CARASIL pathogenesis.
Liu J; Dong F; Hoh J
Proc Natl Acad Sci U S A; 2015 Apr; 112(14):E1693. PubMed ID: 25770224
[No Abstract] [Full Text] [Related]
56. Two Unique Mutations in HTRA1-Related Cerebral Small Vessel Disease in North America and Africa and Literature Review.
Shang T; Pinho M; Ray D; Khera A
J Stroke Cerebrovasc Dis; 2021 Nov; 30(11):106029. PubMed ID: 34461444
[TBL] [Abstract][Full Text] [Related]
57. HTRA1 Mutations Identified in Symptomatic Carriers Have the Property of Interfering the Trimer-Dependent Activation Cascade.
Uemura M; Nozaki H; Koyama A; Sakai N; Ando S; Kanazawa M; Kato T; Onodera O
Front Neurol; 2019; 10():693. PubMed ID: 31316458
[No Abstract] [Full Text] [Related]
58. Hereditary cerebral small vessel diseases: a review.
Federico A; Di Donato I; Bianchi S; Di Palma C; Taglia I; Dotti MT
J Neurol Sci; 2012 Nov; 322(1-2):25-30. PubMed ID: 22868088
[TBL] [Abstract][Full Text] [Related]
59. Monogenic cerebral small-vessel diseases: diagnosis and therapy. Consensus recommendations of the European Academy of Neurology.
Mancuso M; Arnold M; Bersano A; Burlina A; Chabriat H; Debette S; Enzinger C; Federico A; Filla A; Finsterer J; Hunt D; Lesnik Oberstein S; Tournier-Lasserve E; Markus HS
Eur J Neurol; 2020 Jun; 27(6):909-927. PubMed ID: 32196841
[TBL] [Abstract][Full Text] [Related]
60.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
