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Journal Abstract Search

389 related items for PubMed ID: 9577387

  • 1. The natural history of degenerative ataxia: a retrospective study in 466 patients.
    Klockgether T, Lüdtke R, Kramer B, Abele M, Bürk K, Schöls L, Riess O, Laccone F, Boesch S, Lopes-Cendes I, Brice A, Inzelberg R, Zilber N, Dichgans J.
    Brain; 1998 Apr; 121 ( Pt 4)():589-600. PubMed ID: 9577387
    [Abstract] [Full Text] [Related]

  • 2. The role of the SCA2 trinucleotide repeat expansion in 89 autosomal dominant cerebellar ataxia families. Frequency, clinical and genetic correlates.
    Giunti P, Sabbadini G, Sweeney MG, Davis MB, Veneziano L, Mantuano E, Federico A, Plasmati R, Frontali M, Wood NW.
    Brain; 1998 Mar; 121 ( Pt 3)():459-67. PubMed ID: 9549522
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  • 3. Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.
    Klockgether T, Skalej M, Wedekind D, Luft AR, Welte D, Schulz JB, Abele M, Bürk K, Laccone F, Brice A, Dichgans J.
    Brain; 1998 Sep; 121 ( Pt 9)():1687-93. PubMed ID: 9762957
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  • 4. [Clinico-genetic study of type I spinocerebelllar ataxia].
    Svetel M, Culjković B, Sternić N, Dragasević B, Stojković I, Romac S, Kostić VS.
    Srp Arh Celok Lek; 1999 Sep; 127(5-6):157-62. PubMed ID: 10500422
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  • 20. 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
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