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Journal Abstract Search

582 related items for PubMed ID: 25692567

  • 1. Clinical significance of cerebral microbleeds locations in CADASIL with R544C NOTCH3 mutation.
    Lee JS, Kang CH, Park SQ, Choi HA, Sim KB.
    PLoS One; 2015; 10(2):e0118163. PubMed ID: 25692567
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  • 2. R558C NOTCH3 Mutation in a CADASIL Patient with Intracerebral Hemorrhage: A Case Report with Literature Review.
    Hu L, Liu G, Fan Y.
    J Stroke Cerebrovasc Dis; 2022 Jul; 31(7):106541. PubMed ID: 35523050
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  • 4. Characteristics of CADASIL in Korea: a novel cysteine-sparing Notch3 mutation.
    Kim Y, Choi EJ, Choi CG, Kim G, Choi JH, Yoo HW, Kim JS.
    Neurology; 2006 May 23; 66(10):1511-6. PubMed ID: 16717210
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  • 5. Spontaneous cerebellar hemorrhage associated with a novel Notch3 mutation.
    Mehta S, Mehndiratta P, Sila CA.
    J Clin Neurosci; 2013 Jul 23; 20(7):1034-6. PubMed ID: 23623146
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  • 7. CADASIL.
    Hervé D, Chabriat H.
    J Geriatr Psychiatry Neurol; 2010 Dec 23; 23(4):269-76. PubMed ID: 21045164
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  • 8. Intracerebral Hemorrhage in Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy: Prevalence, Clinical and Neuroimaging Features and Risk Factors.
    Liao YC, Hu YC, Chung CP, Wang YF, Guo YC, Tsai YS, Lee YC.
    Stroke; 2021 Mar 23; 52(3):985-993. PubMed ID: 33535780
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  • 9. Three-tesla magnetic resonance imaging study of cerebral microbleeds in patients with ischemic stroke.
    Han J, Gao P, Lin Y, Zhang J, Xu L, Xue J.
    Neurol Res; 2009 Nov 23; 31(9):900-3. PubMed ID: 19138465
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  • 10. Lacunar infarcts are the main correlate with cognitive dysfunction in CADASIL.
    Liem MK, van der Grond J, Haan J, van den Boom R, Ferrari MD, Knaap YM, Breuning MH, van Buchem MA, Middelkoop HA, Lesnik Oberstein SA.
    Stroke; 2007 Mar 23; 38(3):923-8. PubMed ID: 17272761
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  • 11. Cerebral hemorrhages in CADASIL: report of four cases and a brief review.
    Rinnoci V, Nannucci S, Valenti R, Donnini I, Bianchi S, Pescini F, Dotti MT, Federico A, Inzitari D, Pantoni L.
    J Neurol Sci; 2013 Jul 15; 330(1-2):45-51. PubMed ID: 23639391
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  • 13. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese.
    Lee YC, Yang AH, Liu HC, Wong WJ, Lu YC, Chang MH, Soong BW.
    J Neurol Sci; 2006 Jul 15; 246(1-2):111-5. PubMed ID: 16580020
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  • 17. Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese.
    Lee YC, Liu CS, Chang MH, Lin KP, Fuh JL, Lu YC, Liu YF, Soong BW.
    J Neurol; 2009 Feb 15; 256(2):249-55. PubMed ID: 19242647
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  • 18. New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).
    Abramycheva N, Stepanova M, Kalashnikova L, Zakharova M, Maximova M, Tanashyan M, Lagoda O, Fedotova E, Klyushnikov S, Konovalov R, Sakharova A, Illarioshkin S.
    J Neurol Sci; 2015 Feb 15; 349(1-2):196-201. PubMed ID: 25623805
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  • 19. CADASIL with a novel NOTCH3 mutation (Cys478Tyr).
    Ozaki K, Irioka T, Ishikawa K, Mizusawa H.
    J Stroke Cerebrovasc Dis; 2015 Mar 15; 24(3):e61-2. PubMed ID: 25595846
    [Abstract] [Full Text] [Related]

  • 20. Intracerebral hemorrhages in CADASIL.
    Choi JC, Kang SY, Kang JH, Park JK.
    Neurology; 2006 Dec 12; 67(11):2042-4. PubMed ID: 17135568
    [Abstract] [Full Text] [Related]

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