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Journal Abstract Search

819 related items for PubMed ID: 18787576

  • 21. [Chronic ataxia in childhood].
    Erazo Torricelli R.
    Medicina (B Aires); 2013; 73 Suppl 1():38-48. PubMed ID: 24072050
    [Abstract] [Full Text] [Related]

  • 22. Spinocerebellar ataxias.
    Teive HA.
    Arq Neuropsiquiatr; 2009 Dec; 67(4):1133-42. PubMed ID: 20069236
    [Abstract] [Full Text] [Related]

  • 23. Genetic cerebellar ataxias.
    Storey E.
    Semin Neurol; 2014 Jul; 34(3):280-92. PubMed ID: 25192506
    [Abstract] [Full Text] [Related]

  • 24. Cerebellar and afferent ataxias.
    Pandolfo M, Manto M.
    Continuum (Minneap Minn); 2013 Oct; 19(5 Movement Disorders):1312-43. PubMed ID: 24092292
    [Abstract] [Full Text] [Related]

  • 25. [Ataxias. Diagnostic procedure and treatment].
    Klockgether T.
    Nervenarzt; 2005 Oct; 76(10):1275-83; quiz 1284-5. PubMed ID: 16175415
    [Abstract] [Full Text] [Related]

  • 26. 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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  • 27. Neurological approaches to the inherited ataxias.
    Refsum S, Skre H.
    Adv Neurol; 1978 Jun; 21():1-13. PubMed ID: 367114
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  • 30. [Recessive hereditary ataxia with early onset. Clinical study of 27 cases].
    Serlenga L, Trizio M, Pozio G, Oteri G, Caldarazzo M.
    Riv Neurol; 1987 Jun; 57(5):285-9. PubMed ID: 3445070
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  • 31. 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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  • 34. Clinical features and molecular genetics of autosomal recessive cerebellar ataxias.
    Fogel BL, Perlman S.
    Lancet Neurol; 2007 Mar 08; 6(3):245-57. PubMed ID: 17303531
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  • 35. Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients.
    Dragasević NT, Culjković B, Klein C, Ristić A, Keckarević M, Topisirović I, Vukosavić S, Svetel M, Kock N, Stefanova E, Romac S, Kostić VS.
    Mov Disord; 2006 Feb 08; 21(2):187-91. PubMed ID: 16149098
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  • 36. [The genetics of movement disorders--spinocerebellar degenerations].
    Tallaksen CM, Dietrichs E.
    Tidsskr Nor Laegeforen; 2004 Sep 09; 124(17):2233-5. PubMed ID: 15356686
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  • 38. Cerebellar ataxia with spasmodic cough: a new form of dominant ataxia.
    Coutinho P, Cruz VT, Tuna A, Silva SE, Guimarães J.
    Arch Neurol; 2006 Apr 09; 63(4):553-5. PubMed ID: 16606768
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  • 39. [Recent advance in genetic study of hereditary autosomal recessive cerebellar ataxia].
    Guan WJ, Wang JL, Tang BS.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec 09; 29(6):673-6. PubMed ID: 23225047
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  • 40. [Peripheral neuropathies associated with hereditary cerebellar ataxias].
    Anheim M, Tranchant C.
    Rev Neurol (Paris); 2011 Jan 09; 167(1):72-6. PubMed ID: 21195440
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