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Journal Abstract Search

316 related items for PubMed ID: 19139365

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. 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 10; 38(3):923-8. PubMed ID: 17272761
    [Abstract] [Full Text] [Related]

  • 4. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: progression of MR abnormalities in prospective 7-year follow-up study.
    Liem MK, Lesnik Oberstein SA, Haan J, van der Neut IL, van den Boom R, Ferrari MD, van Buchem MA, van der Grond J.
    Radiology; 2008 Dec 10; 249(3):964-71. PubMed ID: 18840792
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6.
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  • 7. A pathogenic mutation on exon 21 of the NOTCH3 gene causing CADASIL in an octogenarian paucisymptomatic patient.
    Pescini F, Bianchi S, Salvadori E, Poggesi A, Dotti MT, Federico A, Inzitari D, Pantoni L.
    J Neurol Sci; 2008 Apr 15; 267(1-2):170-3. PubMed ID: 18022198
    [Abstract] [Full Text] [Related]

  • 8. Three-dimensional MRI analysis of individual volume of Lacunes in CADASIL.
    Hervé D, Godin O, Dufouil C, Viswanathan A, Jouvent E, Pachaï C, Guichard JP, Bousser MG, Dichgans M, Chabriat H.
    Stroke; 2009 Jan 15; 40(1):124-8. PubMed ID: 18948610
    [Abstract] [Full Text] [Related]

  • 9. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Lesnik Oberstein SA, Haan J.
    Panminerva Med; 2004 Dec 15; 46(4):265-76. PubMed ID: 15876982
    [Abstract] [Full Text] [Related]

  • 10. Childhood-onset CADASIL: clinical, imaging, and neurocognitive features.
    Hartley J, Westmacott R, Decker J, Shroff M, Yoon G.
    J Child Neurol; 2010 May 15; 25(5):623-7. PubMed ID: 20197270
    [Abstract] [Full Text] [Related]

  • 11. 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
    [Abstract] [Full Text] [Related]

  • 12. [Monitoring cognitive characteristics in a population with hereditary cerebrovascular disease (CADASIL) in Colombia].
    Henao-Arboleda E, Aguirre-Acevedo DC, Pacheco C, Yamile-Bocanegra O, Lopera F.
    Rev Neurol; 2009 Apr 15; 45(12):729-33. PubMed ID: 18075987
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 23(3):e241-2. PubMed ID: 24295602
    [Abstract] [Full Text] [Related]

  • 14. Cadasil.
    Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser MG.
    Lancet Neurol; 2009 Jul 15; 8(7):643-53. PubMed ID: 19539236
    [Abstract] [Full Text] [Related]

  • 15. Conventional MRI and NOTCH3 gene screening in sporadic CADASIL.
    Liguori M, Mazzei R, Ungaro C, Simone IL, Gambardella A, Plasmati I, Fera F, Aguglia U, Lanza P, Bono F, Chiumarulo L, Conforti FL, Consoli D, Quattrone A.
    Neurology; 2009 Feb 03; 72(5):469-71. PubMed ID: 19056668
    [No Abstract] [Full Text] [Related]

  • 16. Lenticulostriate arterial lumina are normal in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a high-field in vivo MRI study.
    Liem MK, van der Grond J, Versluis MJ, Haan J, Webb AG, Ferrari MD, van Buchem MA, Lesnik Oberstein SA.
    Stroke; 2010 Dec 03; 41(12):2812-6. PubMed ID: 20966419
    [Abstract] [Full Text] [Related]

  • 17. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
    Ueda M, Nakaguma R, Ando Y.
    Rinsho Byori; 2009 Mar 03; 57(3):242-51. PubMed ID: 19363995
    [Abstract] [Full Text] [Related]

  • 18. Brain atrophy is related to lacunar lesions and tissue microstructural changes in CADASIL.
    Jouvent E, Viswanathan A, Mangin JF, O'Sullivan M, Guichard JP, Gschwendtner A, Cumurciuc R, Buffon F, Peters N, Pachaï C, Bousser MG, Dichgans M, Chabriat H.
    Stroke; 2007 Jun 03; 38(6):1786-90. PubMed ID: 17446424
    [Abstract] [Full Text] [Related]

  • 19. Spontaneous cerebellar hemorrhage associated with a novel Notch3 mutation.
    Mehta S, Mehndiratta P, Sila CA.
    J Clin Neurosci; 2013 Jul 03; 20(7):1034-6. PubMed ID: 23623146
    [Abstract] [Full Text] [Related]

  • 20. 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 03; 256(2):249-55. PubMed ID: 19242647
    [Abstract] [Full Text] [Related]

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