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Journal Abstract Search

237 related items for PubMed ID: 11080925

  • 1. [A case of symptomatic cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
    Nakamizo A, Koga H, Uyama E, Yamabe K.
    Fukuoka Igaku Zasshi; 2000 Sep; 91(9):239-42. PubMed ID: 11080925
    [Abstract] [Full Text] [Related]

  • 2. Mutation of the Notch 3 gene in a Thai cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy family.
    Suwanwela N, Srikiatkhachorn A, Tangwongchai S, Phanthumchina K, Suwanwela N.
    J Med Assoc Thai; 2003 Feb; 86(2):178-82. PubMed ID: 12678157
    [Abstract] [Full Text] [Related]

  • 3. [Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk].
    Yamada H, Yasuda T, Kotorii S, Takahashi K, Tabira T, Sunada Y.
    Rinsho Shinkeigaku; 2001 Feb; 41(2-3):144-6. PubMed ID: 11481859
    [Abstract] [Full Text] [Related]

  • 4. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12.
    Tournier-Lasserve E, Joutel A, Melki J, Weissenbach J, Lathrop GM, Chabriat H, Mas JL, Cabanis EA, Baudrimont M, Maciazek J.
    Nat Genet; 1993 Mar; 3(3):256-9. PubMed ID: 8485581
    [Abstract] [Full Text] [Related]

  • 5. Subcortical angiopathic encephalopathy in a German kindred suggests an autosomal dominant disorder distinct from CADASIL.
    Hagel C, Groden C, Niemeyer R, Stavrou D, Colmant HJ.
    Acta Neuropathol; 2004 Sep; 108(3):231-40. PubMed ID: 15221337
    [Abstract] [Full Text] [Related]

  • 6. [Hereditary CADASIL cerebral arteriopathy. Report of a family].
    Mayer M, Dichgans M, Gasser T, Büttner U, Uttner I, Straube A.
    Nervenarzt; 1995 Dec; 66(12):927-32. PubMed ID: 8584078
    [Abstract] [Full Text] [Related]

  • 7. [From gene to disease; from Notch3 to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
    Oberstein SA, Bakker E, Ferrari MD, Haan J.
    Ned Tijdschr Geneeskd; 2001 Feb 24; 145(8):359-60. PubMed ID: 11257815
    [Abstract] [Full Text] [Related]

  • 8. CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Ruchoux MM, Maurage CA.
    J Neuropathol Exp Neurol; 1997 Sep 24; 56(9):947-64. PubMed ID: 9291937
    [Abstract] [Full Text] [Related]

  • 9. [Japanese CADASIL case with limited dementia who had the Notch 3 R141C mutation].
    Ishibashi K, Murata T, Miki Y, Hara M, Mori H.
    No To Shinkei; 2005 May 24; 57(5):415-8. PubMed ID: 15981641
    [Abstract] [Full Text] [Related]

  • 10. [Cerebral arteriopathy with subcortical infarctions and leukoencephalopathy with dominant autosomal inheritance (CADASIL). Clinical and morphological study].
    Marrero Falcón C, Díez Tejedor E, Arpa Gutiérrez J, Barreiro Tella P.
    Neurologia; 1999 May 24; 14(6):275-82. PubMed ID: 10439621
    [Abstract] [Full Text] [Related]

  • 11. Role of subvoxel free fluid on diffusion parameters in brain tissue with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and its correlation with physical disability: histogram analysis of standard and fluid-attenuated MR diffusion.
    Dichgans M, Pütz B, Boos D, Auer DP.
    AJNR Am J Neuroradiol; 2003 May 24; 24(6):1083-9. PubMed ID: 12812930
    [Abstract] [Full Text] [Related]

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  • 13. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
    Otori T, Katayama Y.
    Nihon Rinsho; 2004 Jan 24; 62 Suppl():331-4. PubMed ID: 15011378
    [No Abstract] [Full Text] [Related]

  • 14. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Sung PS, Pai MC.
    Acta Neurol Taiwan; 2008 Dec 24; 17(4):295-6. PubMed ID: 19280875
    [No Abstract] [Full Text] [Related]

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  • 16. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) presenting with sudden sensorineural hearing loss.
    Phillips JS, King JA, Chandran S, Prinsley PR, Dick D.
    J Laryngol Otol; 2005 Feb 24; 119(2):148-51. PubMed ID: 15829071
    [Abstract] [Full Text] [Related]

  • 17. Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL).
    Hutchinson M, O'Riordan J, Javed M, Quin E, Macerlaine D, Wilcox T, Parfrey N, Nagy TG, Tournier-Lasserve E.
    Ann Neurol; 1995 Nov 24; 38(5):817-24. PubMed ID: 7486874
    [Abstract] [Full Text] [Related]

  • 18. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL): a case report with review of literature.
    Gurumukhani JK, Ursekar M, Singhal BS.
    Neurol India; 2004 Mar 24; 52(1):99-101. PubMed ID: 15069251
    [Abstract] [Full Text] [Related]

  • 19. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Soong BW, Lee YC, Lu YC.
    Hum Genet; 2005 Feb 24; 116(3):242. PubMed ID: 15818833
    [No Abstract] [Full Text] [Related]

  • 20. [A case of CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and lekoencephalopathy) with Notch 3 (Arg169Cys) mutation and typical granular osmiophilic materials in peripheral small arteries].
    Kotani N, Hara H, Fujimura H, Miyashita T, Miyaguchi K, Tabira T.
    Rinsho Shinkeigaku; 2004 Feb 24; 44(4-5):274-9. PubMed ID: 15287509
    [Abstract] [Full Text] [Related]

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