BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 26138950)

  • 1. 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]  

  • 2. Features of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy.
    Nozaki H; Nishizawa M; Onodera O
    Stroke; 2014 Nov; 45(11):3447-53. PubMed ID: 25116877
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. A CARASIL Patient from Americas with Novel Mutation and Atypical Features: Case Presentation and Literature Review.
    Ibrahimi M; Nozaki H; Lee A; Onodera O; Reichwein R; Wicklund M; El-Ghanem M
    Cerebrovasc Dis; 2017; 44(3-4):135-140. PubMed ID: 28628911
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel HTRA1 exon 2 mutation causes loss of protease activity in a Pakistani CARASIL patient.
    Khaleeli Z; Jaunmuktane Z; Beaufort N; Houlden H; Haffner C; Brandner S; Dichgans M; Werring D
    J Neurol; 2015 May; 262(5):1369-72. PubMed ID: 25957642
    [No Abstract]   [Full Text] [Related]  

  • 6. 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]  

  • 7. [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]  

  • 8. 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]  

  • 9. Cerebral small vessel disease-related protease HtrA1 processes latent TGF-β binding protein 1 and facilitates TGF-β signaling.
    Beaufort N; Scharrer E; Kremmer E; Lux V; Ehrmann M; Huber R; Houlden H; Werring D; Haffner C; Dichgans M
    Proc Natl Acad Sci U S A; 2014 Nov; 111(46):16496-501. PubMed ID: 25369932
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. Deep Gray Matter Iron Deposition and Its Relationship to Clinical Features in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Patients: A 7.0-T Magnetic Resonance Imaging Study.
    Sun C; Wu Y; Ling C; Xie Z; Kong Q; Fang X; An J; Sun Y; Zhang W; Yang Q; Wang Z; Zhang Z; Yuan Y
    Stroke; 2020 Jun; 51(6):1750-1757. PubMed ID: 32397933
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population.
    Cai B; Zeng J; Lin Y; Lin Y; Lin W; Lin W; Li Z; Wang N
    Neurol Sci; 2015 Aug; 36(8):1387-91. PubMed ID: 25772074
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Two novel HTRA1 mutations in a European CARASIL patient.
    Bianchi S; Di Palma C; Gallus GN; Taglia I; Poggiani A; Rosini F; Rufa A; Muresanu DF; Cerase A; Dotti MT; Federico A
    Neurology; 2014 Mar; 82(10):898-900. PubMed ID: 24500651
    [No Abstract]   [Full Text] [Related]  

  • 16. One Disease with two Faces: Semidominant Inheritance of a Novel HTRA1 Mutation in a Consanguineous Family.
    Bekircan-Kurt CE; Çetinkaya A; Gocmen R; Koşukcu C; Soylemezoglu F; Arsava EM; Tuncer A; Erdem-Ozdamar S; Akarsu NA; Topcuoglu MA
    J Stroke Cerebrovasc Dis; 2021 Sep; 30(9):105997. PubMed ID: 34303089
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Mutation in the HTRA1 gene in a patient with degenerated spine as a component of CARASIL syndrome.
    Bayrakli F; Balaban H; Gurelik M; Hizmetli S; Topaktas S
    Turk Neurosurg; 2014; 24(1):67-9. PubMed ID: 24535794
    [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. 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]  

    [Next]    [New Search]
    of 10.