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Journal Abstract Search

80 related items for PubMed ID: 3921817

  • 1. The inherited ataxias.
    Stumpf DA.
    Neurol Clin; 1985 Feb; 3(1):47-57. PubMed ID: 3921817
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  • 2. The inherited ataxias.
    Harding AE.
    Adv Neurol; 1988 Feb; 48():37-46. PubMed ID: 3275441
    [No Abstract] [Full Text] [Related]

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  • 5. A novel mutation in the dihydrolipoamide dehydrogenase E3 subunit gene (DLD) resulting in an atypical form of alpha-ketoglutarate dehydrogenase deficiency.
    Odièvre MH, Chretien D, Munnich A, Robinson BH, Dumoulin R, Masmoudi S, Kadhom N, Rötig A, Rustin P, Bonnefont JP.
    Hum Mutat; 2005 Mar; 25(3):323-4. PubMed ID: 15712224
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  • 6. Pyruvate dehydrogenase deficiency in spinocerebellar degenerations.
    Kark RA, Rodriguez-Budelli M.
    Neurology; 1979 Jan; 29(1):126-31. PubMed ID: 106330
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  • 8. Molecular genetics of hereditary ataxias.
    Banfi S, Zoghbi HY.
    Baillieres Clin Neurol; 1994 Aug; 3(2):281-95. PubMed ID: 7952848
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  • 12. Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxia.
    Debray FG, Lambert M, Gagne R, Maranda B, Laframboise R, MacKay N, Robinson BH, Mitchell GA.
    Neuropediatrics; 2008 Feb; 39(1):20-3. PubMed ID: 18504677
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  • 14. [Disorders of pyruvate metabolism and TCA cycle].
    Kuroda Y.
    Ryoikibetsu Shokogun Shirizu; 2001 Feb; (36):95-9. PubMed ID: 11596462
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  • 15. Ataxia with isolated vitamin E deficiency: a treatable neurologic disorder resembling Friedreich's ataxia.
    Federico A.
    Neurol Sci; 2004 Jul; 25(3):119-21. PubMed ID: 15300458
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  • 18. Disorders of pyruvate metabolism and the tricarboxylic acid cycle.
    Pithukpakorn M.
    Mol Genet Metab; 2005 Aug; 85(4):243-6. PubMed ID: 16156009
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  • 20. [Cardiac manifestations of Friedreich's ataxia].
    Kolek M, Mrózek V, Schenk P.
    Cas Lek Cesk; 2004 Aug; 143(1):48-51. PubMed ID: 15061120
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