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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

138 related items for PubMed ID: 1665760

  • 21. [SAC1 and SAC2: disease loci, gene defect, and clinical phenotypes].
    Sasaki H, Tashiro K, Wakisaka A.
    No To Shinkei; 1995 Feb; 47(2):109-16. PubMed ID: 7669409
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  • 22. Heterogeneous findings in four cases of cerebellar ataxia associated with hypogonadism (Holmes' type ataxia).
    De Michele G, Filla A, Striano S, Rimoldi M, Campanella G.
    Clin Neurol Neurosurg; 1993 Mar; 95(1):23-8. PubMed ID: 8453811
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  • 25. [Olivocerebellar atrophy predominantly affecting the vermis (clinical and etiopathogenic aspects apropos of 34 cases)].
    Ka M, Kone S, Ndiaye M, Ndiaye IP.
    Dakar Med; 1988 Mar; 33(1-4):30-5. PubMed ID: 3079273
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  • 30. Magnetic resonance imaging in the diagnosis of dominantly inherited cerebello-olivary atrophy: a clinicopathologic study.
    Bonni A, del Carpio-O'Donovan R, Robitaille Y, Andermann E, Andermann F, Arnold DA.
    Can Assoc Radiol J; 1993 Jun; 44(3):194-8. PubMed ID: 8504332
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  • 33. An extended phenotype of an early-onset inherited nonprogressive cerebellar ataxia syndrome.
    Kornberg AJ, Shield LK.
    J Child Neurol; 1991 Jan; 6(1):20-3. PubMed ID: 2002196
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  • 34. Clinical and molecular features of spinocerebellar ataxia type 6.
    Stevanin G, Dürr A, David G, Didierjean O, Cancel G, Rivaud S, Tourbah A, Warter JM, Agid Y, Brice A.
    Neurology; 1997 Nov; 49(5):1243-6. PubMed ID: 9371901
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  • 35. Abnormal ocular motor function predicts clinical diagnosis of familial ataxia.
    Hutton JT, Albrecht JW, Kuskowski M, Schut LJ.
    Neurology; 1987 Apr; 37(4):698-701. PubMed ID: 3470630
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  • 37. Electroencephalographic findings of hereditary dentatorubral-pallidoluysian atrophy (DRPLA).
    Inazuki G, Baba K, Naito H.
    Jpn J Psychiatry Neurol; 1989 Jun; 43(2):213-20. PubMed ID: 2529387
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