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Journal Abstract Search

1135 related items for PubMed ID: 23622410

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  • 3. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
    Ben Hamida M, Attia-Romdhane N, Triki CH, Oueslati S, Hentati F.
    Rev Neurol (Paris); 1991; 147(12):798-808. PubMed ID: 1780608
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  • 4. [Chronic ataxia in childhood].
    Erazo Torricelli R.
    Medicina (B Aires); 2013; 73 Suppl 1():38-48. PubMed ID: 24072050
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  • 7. 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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  • 8. The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias.
    Di Donato S, Gellera C, Mariotti C.
    Neurol Sci; 2001 Jun; 22(3):219-28. PubMed ID: 11731874
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  • 12. Brain phospholipids and fatty acids in Friedreich's ataxia and spinocerebellar atrophy type-1.
    Eder K, Kish SJ, Kirchgessner M, Ross BM.
    Mov Disord; 1998 Sep; 13(5):813-9. PubMed ID: 9756151
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  • 13. [Friedreich ataxia--diagnosis after a decade. Differential diagnosis of inherited spinocerebellar ataxias].
    Vitaszil E, Jelencsik I, Szirmai I.
    Ideggyogy Sz; 2002 Nov 20; 55(11-12):382-93. PubMed ID: 12632799
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  • 14. Hereditary ataxias: overview.
    Jayadev S, Bird TD.
    Genet Med; 2013 Sep 20; 15(9):673-83. PubMed ID: 23538602
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  • 18. Parkinsonism & related disorders. Ataxias.
    Klockgether T.
    Parkinsonism Relat Disord; 2007 Sep 20; 13 Suppl 3():S391-4. PubMed ID: 18267270
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  • 19. Diagnosis and management of early- and late-onset cerebellar ataxia.
    Brusse E, Maat-Kievit JA, van Swieten JC.
    Clin Genet; 2007 Jan 20; 71(1):12-24. PubMed ID: 17204042
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  • 20. Quantification of circulating plasma DNA in Friedreich's ataxia and spinocerebellar ataxia types 2 and 12.
    Swarup V, Srivastava AK, Padma MV, Rajeswari MR.
    DNA Cell Biol; 2011 Jun 20; 30(6):389-94. PubMed ID: 21329459
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