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Journal Abstract Search

124 related items for PubMed ID: 3463881

  • 21. Olivopontocerebellar atrophy in a large Iakut kinship in eastern Siberia.
    Goldfarb LG, Chumakov MP, Petrov PA, Fedorova NI, Gajdusek DC.
    Neurology; 1989 Nov; 39(11):1527-30. PubMed ID: 2812335
    [Abstract] [Full Text] [Related]

  • 22. X-linked olivopontocerebellar atrophy.
    Lutz R, Bodensteiner J, Schaefer B, Gay C.
    Clin Genet; 1989 Jun; 35(6):417-22. PubMed ID: 2661059
    [Abstract] [Full Text] [Related]

  • 23. Cerebellar ataxia, dementia, pyramidal signs, cortical cataract of the posterior pole and a raised IgG index in a patient with a sporadic form of olivopontocerebellar atrophy.
    Schelhaas HJ, Hageman G, Post JG.
    Clin Neurol Neurosurg; 1997 May; 99(2):99-101. PubMed ID: 9213052
    [Abstract] [Full Text] [Related]

  • 24. Heredo-ataxia in a large Dutch pedigree. M.R.I. findings.
    Vliegenthart WE, Vielvoye GJ, Kuyt LP.
    Clin Neurol Neurosurg; 1991 May; 93(4):275-81. PubMed ID: 1665760
    [Abstract] [Full Text] [Related]

  • 25. Motor evoked potentials by magnetic stimulation in hereditary and sporadic ataxia.
    Mondelli M, Rossi A, Scarpini C, Guazzi GC.
    Electromyogr Clin Neurophysiol; 1995 Nov; 35(7):415-24. PubMed ID: 8549432
    [Abstract] [Full Text] [Related]

  • 26. [Clinical types of spinocerebellar degeneration and evaluation with MR imaging].
    Kojima S.
    Rinsho Shinkeigaku; 1993 Dec; 33(12):1294-6. PubMed ID: 8174328
    [Abstract] [Full Text] [Related]

  • 27. [Study on argyrophilic inclusions of multisystem atrophy (Oppenheimer)].
    Iwabuchi K, Kosaka K, Haga C, Tuchiya K, Amano N, Itoh K, Yagishita S, Mizutani Y.
    No To Shinkei; 1991 Jun; 43(6):561-8. PubMed ID: 1654964
    [Abstract] [Full Text] [Related]

  • 28. Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
    Gomez CM, Thompson RM, Gammack JT, Perlman SL, Dobyns WB, Truwit CL, Zee DS, Clark HB, Anderson JH.
    Ann Neurol; 1997 Dec; 42(6):933-50. PubMed ID: 9403487
    [Abstract] [Full Text] [Related]

  • 29. Pure cerebello-olivary degeneration of Marie, Foix, and Alajouanine presenting with progressive cerebellar ataxia, cognitive decline, and chorea.
    Fox SH, Nieves A, Bergeron C, Lang AE.
    Mov Disord; 2003 Dec; 18(12):1550-4. PubMed ID: 14673899
    [Abstract] [Full Text] [Related]

  • 30. CT in autosomal dominant and idiopathic cerebellar ataxia.
    Wittkämper A, Wessel K, Brückmann H.
    Neuroradiology; 1993 Dec; 35(7):520-4. PubMed ID: 8232880
    [Abstract] [Full Text] [Related]

  • 31. Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type I.
    Benomar A, Le Guern E, Dürr A, Ouhabi H, Stevanin G, Yahyaoui M, Chkili T, Agid Y, Brice A.
    Ann Neurol; 1994 Apr; 35(4):439-44. PubMed ID: 8154871
    [Abstract] [Full Text] [Related]

  • 32. Autosomal-dominant dentatorubropallidoluysian atrophy in the United Kingdom.
    Warner TT, Lennox GG, Janota I, Harding AE.
    Mov Disord; 1994 May; 9(3):289-96. PubMed ID: 8041369
    [Abstract] [Full Text] [Related]

  • 33. Dominantly inherited hypoplasia of the vermis.
    Rivier F, Echenne B.
    Neuropediatrics; 1992 Aug; 23(4):206-8. PubMed ID: 1407388
    [Abstract] [Full Text] [Related]

  • 34. [A family with Menzel's disease showing dementia and various extrapyramidal symptoms].
    Iwabuchi K, Nagatomo H, Tanabe T, Oda T, Itoh H, Hanihara T, Yagishita S.
    No To Shinkei; 1993 Sep; 45(9):841-9. PubMed ID: 8217410
    [Abstract] [Full Text] [Related]

  • 35. [An apparently sporadic case with spinocerebellar ataxia type 1 (SCA1)].
    Futamura N, Matsumura R, Murata K, Suzumura A, Takayanagi T.
    Rinsho Shinkeigaku; 1997 Aug; 37(8):708-10. PubMed ID: 9404150
    [Abstract] [Full Text] [Related]

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  • 38. [Linkage study of hereditary spinocerebellar ataxia, and probable correlation for the loci to the disease phenotypes].
    Sasaki H.
    Rinsho Shinkeigaku; 1993 Dec; 33(12):1285-7. PubMed ID: 8174326
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  • 40. Infantile olivopontocerebellar atrophy with spinal muscular atrophy (infantile OPCA + SMA).
    Chou SM, Gilbert EF, Chun RW, Laxova R, Tuffli GA, Sufit RL, Krassikot N.
    Clin Neuropathol; 1990 Dec; 9(1):21-32. PubMed ID: 2407400
    [Abstract] [Full Text] [Related]

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