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 *

208 related articles for article (PubMed ID: 34433685)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 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. 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]  

  • 6. 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]  

  • 7. Novel c.971A>G mutation in the HTRA1 gene in a Chinese family with CARASIL.
    Hou MM; Mao XW; Liu XB; Liu YQ; Bi XY; Hou XJ
    J Biol Regul Homeost Agents; 2020; 34(4):1407-1410. PubMed ID: 32895092
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. CARASIL - A Review of Patients from India.
    Khandelwal D; Mathur V; Vyas A; Ghunawat J; Bagaria AK
    Neurol India; 2021; 69(5):1359-1362. PubMed ID: 34747813
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.