These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

183 related items for PubMed ID: 6886703

  • 1. Autosomal recessive spino-olivo-cerebellar degeneration without ataxia.
    Staal A, Stefanko SZ, Jennekens FG, Vries-Bos LH, van Gijn J.
    J Neurol Neurosurg Psychiatry; 1983 Jul; 46(7):648-52. PubMed ID: 6886703
    [Abstract] [Full Text] [Related]

  • 2. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.
    Harding AE.
    Brain; 1982 Mar; 105(Pt 1):1-28. PubMed ID: 7066668
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. [Progressive supranuclear palsy with familial occurrence of spinocerebellar degeneration].
    Yamamura Y, Kito S, Itoga E, Kajiwara H.
    Rinsho Shinkeigaku; 1982 Jul; 22(7):586-93. PubMed ID: 7172528
    [No Abstract] [Full Text] [Related]

  • 5. Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia. A unique and partially treatable clinico-pathological entity.
    Woods BT, Schaumburg HH.
    J Neurol Sci; 1972 Oct; 17(2):149-66. PubMed ID: 5053922
    [No Abstract] [Full Text] [Related]

  • 6. Prevalence and pattern of spinocerebellar degenerations in northeastern Libya.
    Sridharan R, Radhakrishnan K, Ashok PP, Mousa ME.
    Brain; 1985 Dec; 108 ( Pt 4)():831-43. PubMed ID: 4075075
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. [Autosomal recessive hereditary cortical cerebellar atrophy with striatal degeneration--two siblings showing choreoathetoid movement, ataxia, dementia, and amenorrhea].
    Iwabuchi K, Nakazawa Y, Akai J, Yagishita S, Amano N.
    No To Shinkei; 1994 Jun; 46(6):563-71. PubMed ID: 8068439
    [Abstract] [Full Text] [Related]

  • 9. A spinocerebellar degeneration with X-linked inheritance.
    Spira PJ, McLeod JG, Evans WA.
    Brain; 1979 Mar; 102(1):27-41. PubMed ID: 427531
    [Abstract] [Full Text] [Related]

  • 10. A novel GBA2 gene missense mutation in spastic ataxia.
    Votsi C, Zamba-Papanicolaou E, Middleton LT, Pantzaris M, Christodoulou K.
    Ann Hum Genet; 2014 Jan; 78(1):13-22. PubMed ID: 24252062
    [Abstract] [Full Text] [Related]

  • 11. [Juvenile autosomal-recessive spastic paraplegia].
    Badalian LO, Iadgarov IS, Arkhipov BA, Temin PA, Bulaeva NV.
    Pediatriia; 1989 Jan; (2):90-2. PubMed ID: 2726376
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Joseph disease: a multisystem degenerative disorder of the nervous system.
    Sachdev HS, Forno LS, Kane CA.
    Neurology; 1982 Feb; 32(2):192-5. PubMed ID: 7198744
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. The pathology of Machado-Joseph disease. Report of a possible homozygous case.
    Coutinho P, Guimarães A, Scaravilli F.
    Acta Neuropathol; 1982 Feb; 58(1):48-54. PubMed ID: 7136516
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.