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

Journal Abstract Search


207 related items for PubMed ID: 1293986

  • 1. [Clinical, multimodal electrophysiological study of a family with progressive cerebellar ataxia and late deafness and an autosomal recessive inheritance].
    Ragno M, Curatola L, Rossi R, Salvolini U.
    Acta Neurol (Napoli); 1992; 14(4-6):431-9. PubMed ID: 1293986
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
    Schöls L, Amoiridis G, Büttner T, Przuntek H, Epplen JT, Riess O.
    Ann Neurol; 1997 Dec; 42(6):924-32. PubMed ID: 9403486
    [Abstract] [Full Text] [Related]

  • 7. Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
    El Euch-Fayache G, Lalani I, Amouri R, Turki I, Ouahchi K, Hung WY, Belal S, Siddique T, Hentati F.
    Arch Neurol; 2003 Jul; 60(7):982-8. PubMed ID: 12873855
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Predominant dystonia with marked cerebellar atrophy: a rare phenotype in familial dystonia.
    Le Ber I, Clot F, Vercueil L, Camuzat A, Viémont M, Benamar N, De Liège P, Ouvrard-Hernandez AM, Pollak P, Stevanin G, Brice A, Dürr A.
    Neurology; 2006 Nov 28; 67(10):1769-73. PubMed ID: 17130408
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. 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]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Peripheral neuropathy in spinocerebellar degenerations.
    McLeod JG, Evans WA.
    Muscle Nerve; 1981 Mar 15; 4(1):51-61. PubMed ID: 7231446
    [Abstract] [Full Text] [Related]

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

  • 16. A family with autosomal dominant spinocerebellar ataxia, with electrophysiological findings.
    Frey HJ, Frey ML, Riekkinen PJ, Tuomola HO.
    Ann Clin Res; 1973 Jun 15; 5(3):163-7. PubMed ID: 4127165
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Infantile cerebellar atrophy.
    Furman JM, Baloh RW, Chugani H, Waluch V, Bradley WG.
    Ann Neurol; 1985 Apr 15; 17(4):399-402. PubMed ID: 4004161
    [Abstract] [Full Text] [Related]

  • 19. Neurophysiological study in a Spanish family with recessive spastic ataxia of Charlevoix-Saguenay.
    García A, Criscuolo C, de Michele G, Berciano J.
    Muscle Nerve; 2008 Jan 15; 37(1):107-10. PubMed ID: 17683082
    [Abstract] [Full Text] [Related]

  • 20. Early onset cerebellar ataxia with retained tendon reflexes (EOCA): an electromyographic study.
    Pal PK, Taly AB, Nagaraja D, Rao S.
    Electromyogr Clin Neurophysiol; 1996 Jan 15; 36(5):287-93. PubMed ID: 8877321
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 11.