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Journal Abstract Search

953 related items for PubMed ID: 19539236

  • 1. Cadasil.
    Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser MG.
    Lancet Neurol; 2009 Jul; 8(7):643-53. PubMed ID: 19539236
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  • 3. [Cadasil and other hereditary small vessel diseases of the brain--increasingly diagnosed conditions underlying familial ischaemic stroke and dementia].
    Gunda B, Chabriat H, Bereczki D.
    Ideggyogy Sz; 2011 Mar 30; 64(3-4):88-100. PubMed ID: 21545006
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  • 6. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Lesnik Oberstein SA, Haan J.
    Panminerva Med; 2004 Dec 30; 46(4):265-76. PubMed ID: 15876982
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  • 7. The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo.
    Monet M, Domenga V, Lemaire B, Souilhol C, Langa F, Babinet C, Gridley T, Tournier-Lasserve E, Cohen-Tannoudji M, Joutel A.
    Hum Mol Genet; 2007 Apr 15; 16(8):982-92. PubMed ID: 17331978
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  • 9. Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain.
    Monet-Leprêtre M, Bardot B, Lemaire B, Domenga V, Godin O, Dichgans M, Tournier-Lasserve E, Cohen-Tannoudji M, Chabriat H, Joutel A.
    Brain; 2009 Jun 15; 132(Pt 6):1601-12. PubMed ID: 19293235
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  • 10. MRI correlates of cognitive decline in CADASIL: a 7-year follow-up study.
    Liem MK, Lesnik Oberstein SA, Haan J, van der Neut IL, Ferrari MD, van Buchem MA, Middelkoop HA, van der Grond J.
    Neurology; 2009 Jan 13; 72(2):143-8. PubMed ID: 19139365
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  • 12. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy without anterior temporal pole involvement: a case report.
    Kobayashi J, Sato S, Okumura K, Miyashita F, Ueda A, Ando Y, Toyoda K.
    J Stroke Cerebrovasc Dis; 2014 Mar 13; 23(3):e241-2. PubMed ID: 24295602
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  • 13. Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients.
    Pantoni L, Pescini F, Nannucci S, Sarti C, Bianchi S, Dotti MT, Federico A, Inzitari D.
    Neurology; 2010 Jan 05; 74(1):57-63. PubMed ID: 20038773
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  • 14. CADASIL.
    Hervé D, Chabriat H.
    J Geriatr Psychiatry Neurol; 2010 Dec 05; 23(4):269-76. PubMed ID: 21045164
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  • 15. A new de novo Notch3 mutation causing CADASIL.
    Coto E, Menéndez M, Navarro R, García-Castro M, Alvarez V.
    Eur J Neurol; 2006 Jun 05; 13(6):628-31. PubMed ID: 16796587
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  • 17. Report of two Chinese families and a review of Mainland Chinese CADASIL patients.
    Yin XZ, Ding MP, Zhang BR, Liu JR, Zhang L, Wang PZ, Zhou FY, Zhao GH.
    J Neurol Sci; 2009 Apr 15; 279(1-2):88-92. PubMed ID: 19167727
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  • 18. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Chabriat H, Bousser MG.
    Handb Clin Neurol; 2008 Apr 15; 89():671-86. PubMed ID: 18631787
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  • 20. Lacunar lesions are independently associated with disability and cognitive impairment in CADASIL.
    Viswanathan A, Gschwendtner A, Guichard JP, Buffon F, Cumurciuc R, O'Sullivan M, Holtmannspötter M, Pachai C, Bousser MG, Dichgans M, Chabriat H.
    Neurology; 2007 Jul 10; 69(2):172-9. PubMed ID: 17620550
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