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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 27163668)

  • 1. Teaching NeuroImages: When alopecia and disk herniations meet vascular leukoencephalopathy: CARASIL.
    Roeben B; Uhrig S; Bender B; Synofzik M
    Neurology; 2016 Apr; 86(15):e166-e167. PubMed ID: 27163668
    [No Abstract]   [Full Text] [Related]  

  • 2. Lumbago and alopecia in a patient with leukodystrophy: think on CARASIL.
    Souza PV; Pinto WB; Oliveira AS
    Arq Neuropsiquiatr; 2016 Jul; 74(7):599-600. PubMed ID: 27487381
    [No Abstract]   [Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. CARASIL, a rare genetic cause of stroke in the young.
    Devaraddi N; Jayalakshmi G; Mutalik NR
    Neurol India; 2018; 66(1):232-234. PubMed ID: 29322992
    [No Abstract]   [Full Text] [Related]  

  • 8. [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]  

  • 9. CARASIL families from India with 3 novel null mutations in the
    Preethish-Kumar V; Nozaki H; Tiwari S; Vengalil S; Bhat M; Prasad C; Onodera O; Uemura M; Doniparthi S; Saini J; Nashi S; Polavarapu K; Nalini A
    Neurology; 2017 Dec; 89(23):2392-2394. PubMed ID: 29101275
    [No Abstract]   [Full Text] [Related]  

  • 10. [Consideration of the pathogenesis of CARASIL].
    Nozaki H
    Rinsho Shinkeigaku; 2012; 52(11):1360-2. PubMed ID: 23196618
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. [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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Teaching NeuroImages: Vanishing white matter ovarioleukodystrophy.
    Mukerji SS; Eichler FS
    Neurology; 2016 Jun; 86(24):e248. PubMed ID: 27298454
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. A Chinese CARASIL Patient Caused by Novel Compound Heterozygous Mutations in HTRA1.
    Xie F; Zhang LS
    J Stroke Cerebrovasc Dis; 2018 Oct; 27(10):2840-2842. PubMed ID: 30068478
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Teaching NeuroImages: rapidly progressive leukoencephalopathy in mitochondrial complex I deficiency.
    Baertling F; Schaper J; Mayatepek E; Distelmaier F
    Neurology; 2013 Jul; 81(2):e10-1. PubMed ID: 23836946
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.