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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

71 related items for PubMed ID: 3465984

  • 1.
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  • 2. [Spinocerebellar ataxia 1--clinical study of 17 patients in a large pedigree].
    Sasaki H, Wakisaka A, Koyama T, Hamada T, Shima K, Tashiro K, Hashimoto K, Miyagishi T.
    No To Shinkei; 1993 Jun; 45(6):502-8. PubMed ID: 8363844
    [Abstract] [Full Text] [Related]

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  • 4. Acetazolamide responsive hereditary paroxysmal ataxia.
    Friedman JH, Hollmann PA.
    Mov Disord; 1987 Jun; 2(1):67-72. PubMed ID: 3332806
    [Abstract] [Full Text] [Related]

  • 5. Hereditary paroxysmal ataxia.
    Micheli F, de Arbelaiz R, Casas Parera I, Fernandez Pardal M, Paradiso G, Matsubara P.
    Mov Disord; 1987 Jun; 2(4):339-41. PubMed ID: 3504560
    [No Abstract] [Full Text] [Related]

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  • 7. A Japanese family with early-onset ataxia with motor and sensory neuropathy.
    Kobayashi S, Takuma H, Murayama S, Sakurai M, Kanazawa I.
    J Neurol Sci; 2007 Mar 15; 254(1-2):44-8. PubMed ID: 17258771
    [Abstract] [Full Text] [Related]

  • 8. [Aberrance analysis of mitochondrial DNA in a family with hereditary ataxia in Guangxi province].
    Wang J, Liu HH, Luo SG.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun 15; 23(3):323-5. PubMed ID: 16767675
    [Abstract] [Full Text] [Related]

  • 9.
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  • 10. Ataxia without telangiectasia masquerading as benign hereditary chorea.
    Klein C, Wenning GK, Quinn NP, Marsden CD.
    Mov Disord; 1996 Mar 15; 11(2):217-20. PubMed ID: 8684395
    [Abstract] [Full Text] [Related]

  • 11. ECT for organic catatonia due to hereditary cerebellar ataxia.
    Folkerts HW, Stadtland C, Reker T.
    J ECT; 1998 Mar 15; 14(1):53-5. PubMed ID: 9661095
    [No Abstract] [Full Text] [Related]

  • 12. Focal dystonia as a presenting sign of spinocerebellar ataxia 17.
    Hagenah JM, Zühlke C, Hellenbroich Y, Heide W, Klein C.
    Mov Disord; 2004 Feb 15; 19(2):217-20. PubMed ID: 14978680
    [Abstract] [Full Text] [Related]

  • 13. Autosomal dominant cerebellar ataxia deafness and narcolepsy.
    Melberg A, Hetta J, Dahl N, Nennesmo I, Bengtsson M, Wibom R, Grant C, Gustavson KH, Lundberg PO.
    J Neurol Sci; 1995 Dec 15; 134(1-2):119-29. PubMed ID: 8747854
    [Abstract] [Full Text] [Related]

  • 14. Anticipation in spinocerebellar ataxia type 2.
    Pulst SM, Nechiporuk A, Starkman S.
    Nat Genet; 1993 Sep 15; 5(1):8-10. PubMed ID: 8220431
    [No Abstract] [Full Text] [Related]

  • 15. Intrafamilial variability in fragile X-associated tremor/ataxia syndrome.
    Peters N, Kamm C, Asmus F, Holinski-Feder E, Kraft E, Dichgans M, Brüning R, Gasser T, Bötzel K.
    Mov Disord; 2006 Jan 15; 21(1):98-102. PubMed ID: 16124012
    [Abstract] [Full Text] [Related]

  • 16. [Clinical studies on a large family of probable Machado-Joseph disease in Japan].
    Takiyama Y, Tanaka Y, Mizuno Y, Yoshida M.
    Rinsho Shinkeigaku; 1987 May 15; 27(5):569-78. PubMed ID: 3476233
    [No Abstract] [Full Text] [Related]

  • 17.
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  • 18. Linkage analysis in spinopontine atrophy: correlation of HLA linkage with phenotypic findings in hereditary ataxia.
    Bale AE, Bale SJ, Schlesinger SL, McFarland HF.
    Am J Med Genet; 1987 Jul 15; 27(3):595-602. PubMed ID: 3477098
    [Abstract] [Full Text] [Related]

  • 19. Epilepsy and paroxysmal movement disorders in families: evidence for shared mechanisms.
    Singh R, Macdonell RA, Scheffer IE, Crossland KM, Berkovic SF.
    Epileptic Disord; 1999 Jun 15; 1(2):93-9. PubMed ID: 10937138
    [Abstract] [Full Text] [Related]

  • 20. Impact of presymptomatic genetic testing for hereditary ataxia and neuromuscular disorders.
    Smith CO, Lipe HP, Bird TD.
    Arch Neurol; 2004 Jun 15; 61(6):875-80. PubMed ID: 15210524
    [Abstract] [Full Text] [Related]

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