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Journal Abstract Search

300 related items for PubMed ID: 9291937

  • 21. [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; 57(5):415-8. PubMed ID: 15981641
    [Abstract] [Full Text] [Related]

  • 22. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a Greek family.
    Mandellos D, Limbitaki G, Papadimitriou A, Anastasopoulos D.
    Neurol Sci; 2005 Oct; 26(4):278-81. PubMed ID: 16193256
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  • 23. [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 Oct; 41(2-3):144-6. PubMed ID: 11481859
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  • 24. Autosomal dominant cerebral arteriopathy: neuropsychiatric syndrome in a family.
    Adair JC, Hart BL, Kornfeld M, Graham GD, Swanda RM, Ptacek LJ, Davis LE.
    Neuropsychiatry Neuropsychol Behav Neurol; 1998 Jan; 11(1):31-9. PubMed ID: 9560826
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  • 26. [The clinical and genetic studies in a family of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].
    Zhang LF, Yang XS, Wang YF, Pei LT.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):187-90. PubMed ID: 19350513
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  • 27. 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
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  • 30. Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Chabriat H, Vahedi K, Iba-Zizen MT, Joutel A, Nibbio A, Nagy TG, Krebs MO, Julien J, Dubois B, Ducrocq X.
    Lancet; 1995 Oct 07; 346(8980):934-9. PubMed ID: 7564728
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  • 31. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
    Otori T, Katayama Y.
    Nihon Rinsho; 2004 Jan 07; 62 Suppl():331-4. PubMed ID: 15011378
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  • 33. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.
    Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E.
    Nature; 1996 Oct 24; 383(6602):707-10. PubMed ID: 8878478
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  • 34. Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus.
    Chabriat H, Tournier-Lasserve E, Vahedi K, Leys D, Joutel A, Nibbio A, Escaillas JP, Iba-Zizen MT, Bracard S, Tehindrazanarivelo A.
    Neurology; 1995 Jun 24; 45(6):1086-91. PubMed ID: 7783868
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  • 35. CADASIL: hereditary disease of arteries causing brain infarcts and dementia.
    Kalimo H, Viitanen M, Amberla K, Juvonen V, Marttila R, Pöyhönen M, Rinne JO, Savontaus M, Tuisku S, Winblad B.
    Neuropathol Appl Neurobiol; 1999 Aug 24; 25(4):257-65. PubMed ID: 10476042
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  • 36. Fibrosis and stenosis of the long penetrating cerebral arteries: the cause of the white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
    Miao Q, Paloneva T, Tuominen S, Pöyhönen M, Tuisku S, Viitanen M, Kalimo H.
    Brain Pathol; 2004 Oct 24; 14(4):358-64. PubMed ID: 15605982
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  • 38. Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine.
    Dichgans M, Mayer M, Müller-Myhsok B, Straube A, Gasser T.
    Genomics; 1996 Feb 15; 32(1):151-4. PubMed ID: 8786108
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  • 39. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) characteristics in Japan: variety of clinical features.
    Adachi Y, Nakashima K.
    Intern Med; 2000 Sep 15; 39(9):681-2. PubMed ID: 10969895
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  • 40. An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
    Ragno M, Tournier-Lasserve E, Fiori MG, Manca A, Patrosso MC, Ferlini A, Sirocchi G, Trojano L, Chabriat H, Salvi F.
    Ann Neurol; 1995 Aug 15; 38(2):231-6. PubMed ID: 7654071
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