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Journal Abstract Search

148 related items for PubMed ID: 8958750

  • 1. [A Japanese family with probably autosomal dominant adult-onset leukodystrophy].
    Asahara H, Yoshimura T, Sada S, Furuya H, Kobayashi T.
    Rinsho Shinkeigaku; 1996 Aug; 36(8):968-72. PubMed ID: 8958750
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  • 2. Hereditary adult-onset leukodystrophy simulating chronic progressive multiple sclerosis.
    Eldridge R, Anayiotos CP, Schlesinger S, Cowen D, Bever C, Patronas N, McFarland H.
    N Engl J Med; 1984 Oct 11; 311(15):948-53. PubMed ID: 6472420
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  • 3. Neurophysiological study in an Italian family with autosomal dominant late-onset leukodystrophy.
    Leombruni S, Vaula G, Coletti Moja M, Bergui M, Bergamini L, Quattrocolo G.
    Electromyogr Clin Neurophysiol; 1998 Oct 11; 38(3):131-5. PubMed ID: 9637937
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  • 4. Autosomal dominant childhood onset slowly progressive leukodystrophy--a Japanese family with spastic paraparesis, ataxia, mental deterioration, and skeletal abnormality.
    Nomoto N, Iwasaki Y, Arasaki K, Fujioka T, Kurihara T, Wakata N.
    J Neurol Sci; 2004 Jun 15; 221(1-2):35-9. PubMed ID: 15178211
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  • 6. [Clinical and genealogical report on a new family with three cases of adult metachromatic leukodystrophy].
    Wildbolz A.
    Schweiz Arch Neurol Neurochir Psychiatr; 1971 Jun 15; 109(2):313-21. PubMed ID: 5145365
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  • 7. A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy.
    Meijer IA, Simoes-Lopes AA, Laurent S, Katz T, St-Onge J, Verlaan DJ, Dupré N, Thibault M, Mathurin J, Bouchard JP, Rouleau GA.
    Arch Neurol; 2008 Nov 15; 65(11):1496-501. PubMed ID: 19001169
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  • 8. Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.
    Sobrido MJ, Fernández JM, Fontoira E, Pérez-Sousa C, Cabello A, Castro M, Teijeira S, Alvarez S, Mederer S, Rivas E, Seijo-Martínez M, Navarro C.
    Brain; 2005 Jul 15; 128(Pt 7):1716-27. PubMed ID: 15857933
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  • 9. Clinical and pathological features of an autosomal dominant, adult-onset leukodystrophy simulating chronic progressive multiple sclerosis.
    Schwankhaus JD, Katz DA, Eldridge R, Schlesinger S, McFarland H.
    Arch Neurol; 1994 Aug 15; 51(8):757-66. PubMed ID: 8042923
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  • 11. [Late cerebellar ataxia associated with fragile X premutation].
    Chaussenot A, Borg M, Bayreuther C, Lebrun C.
    Rev Neurol (Paris); 2008 Nov 15; 164(11):957-63. PubMed ID: 18808779
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  • 13. 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 15; 11(1):31-9. PubMed ID: 9560826
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  • 14. Autosomal dominant leukodystrophy with axonal spheroids and pigmented glia: clinical and neuropathological characteristics.
    Itoh K, Shiga K, Shimizu K, Muranishi M, Nakagawa M, Fushiki S.
    Acta Neuropathol; 2006 Jan 15; 111(1):39-45. PubMed ID: 16328511
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  • 15. A new familial adult-onset leukodystrophy manifesting as cerebellar ataxia and dementia.
    Tagawa A, Ono S, Inoue K, Hosoi N, Kaneda K, Suzuki M, Nagao K, Shimizu N.
    J Neurol Sci; 2001 Jan 15; 183(1):47-55. PubMed ID: 11166794
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  • 20. MR imaging characteristics and neuropathology of the spinal cord in adult-onset autosomal dominant leukodystrophy with autonomic symptoms.
    Sundblom J, Melberg A, Kalimo H, Smits A, Raininko R.
    AJNR Am J Neuroradiol; 2009 Feb 15; 30(2):328-35. PubMed ID: 18945794
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