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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

316 related items for PubMed ID: 7303765

  • 21.
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  • 23. [Distribution of dominant hereditary ataxias and Friedreich's ataxia in the Spanish population].
    Mayo Cabrero D, Hernández Cristóbal J, Cantarero Duque S, Martínez Delgado B, Urioste Azcorra M, Robledo Batanero M, García-Ruiz Espiga P, Benítez Ortiz J.
    Med Clin (Barc); 2000 Jun 24; 115(4):121-5. PubMed ID: 10996881
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  • 25. Cerebellar ataxia in the eastern and southern parts of Norway.
    Koht J, Tallaksen CM.
    Acta Neurol Scand Suppl; 2007 Jun 24; 187():76-9. PubMed ID: 17419835
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  • 26. [Diagnosis: not more than an agreement on disease entity].
    van Gijn J, Walvoort HC.
    Ned Tijdschr Geneeskd; 2002 Sep 07; 146(36):1672-4. PubMed ID: 12244769
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  • 27. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
    Brkanac Z, Fernandez M, Matsushita M, Lipe H, Wolff J, Bird TD, Raskind WH.
    Am J Med Genet; 2002 May 08; 114(4):450-7. PubMed ID: 11992570
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  • 28. Friedreich's ataxia and other hereditary ataxias in Greece: an 18-year perspective.
    Koutsis G, Kladi A, Karadima G, Houlden H, Wood NW, Christodoulou K, Panas M.
    J Neurol Sci; 2014 Jan 15; 336(1-2):87-92. PubMed ID: 24209901
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  • 32. [Study of taurine levels in the blood and urine of patients with hereditary spinocerebellar degeneration].
    Magalov ShI, Arzumanova KG.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990 Jan 15; 90(3):16-20. PubMed ID: 2163160
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  • 34. Cerebellar and afferent ataxias.
    Pandolfo M, Manto M.
    Continuum (Minneap Minn); 2013 Oct 15; 19(5 Movement Disorders):1312-43. PubMed ID: 24092292
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  • 35. Evidence for a primary defect of lipoamide dehydrogenase in Friedreich's ataxia.
    Kark RA, Rodriguez-Budelli M, Blass JP.
    Adv Neurol; 1978 Oct 15; 21():163-80. PubMed ID: 104555
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  • 36. Clinical features of chromosome 16q22.1 linked autosomal dominant cerebellar ataxia in Japanese.
    Onodera Y, Aoki M, Mizuno H, Warita H, Shiga Y, Itoyama Y.
    Neurology; 2006 Oct 10; 67(7):1300-2. PubMed ID: 17030774
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  • 37. The autosomal recessive cerebellar ataxias.
    Anheim M, Tranchant C, Koenig M.
    N Engl J Med; 2012 Feb 16; 366(7):636-46. PubMed ID: 22335741
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  • 38. The inherited cerebellar ataxias: an update.
    Coarelli G, Wirth T, Tranchant C, Koenig M, Durr A, Anheim M.
    J Neurol; 2023 Jan 16; 270(1):208-222. PubMed ID: 36152050
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  • 39. SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
    Faruq M, Scaria V, Singh I, Tyagi S, Srivastava AK, Mukerji M.
    Hum Mutat; 2009 Jul 16; 30(7):1037-42. PubMed ID: 19370769
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