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Journal Abstract Search

310 related items for PubMed ID: 14534930

  • 1. Periodic alternating nystagmus and rebound nystagmus in spinocerebellar ataxia type 6.
    Hashimoto T, Sasaki O, Yoshida K, Takei Y, Ikeda S.
    Mov Disord; 2003 Oct; 18(10):1201-4. PubMed ID: 14534930
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  • 2. Periodic alternating nystagmus and periodic alternating skew deviation in spinocerebellar ataxia type 6.
    Colen CB, Ketko A, George E, Van Stavern GP.
    J Neuroophthalmol; 2008 Dec; 28(4):287-8. PubMed ID: 19145126
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  • 4. [Initial symptoms and mode of neurological progression in spinocerebellar ataxia type 6 (SCA6)].
    Yabe I, Sasaki H, Yamashita I, Takei A, Fukazawa T, Hamada T, Tashiro K.
    Rinsho Shinkeigaku; 1998 Jun; 38(6):489-94. PubMed ID: 9847664
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  • 5. Parkinsonism and nigrostriatal dysfunction are associated with spinocerebellar ataxia type 6 (SCA6).
    Khan NL, Giunti P, Sweeney MG, Scherfler C, Brien MO, Piccini P, Wood NW, Lees AJ.
    Mov Disord; 2005 Sep; 20(9):1115-9. PubMed ID: 15954136
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  • 6. Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.
    Pulst SM, Santos N, Wang D, Yang H, Huynh D, Velazquez L, Figueroa KP.
    Brain; 2005 Oct; 128(Pt 10):2297-303. PubMed ID: 16000334
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  • 7. Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17).
    Hübner J, Sprenger A, Klein C, Hagenah J, Rambold H, Zühlke C, Kömpf D, Rolfs A, Kimmig H, Helmchen C.
    Neurology; 2007 Sep 11; 69(11):1160-8. PubMed ID: 17846415
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  • 8. Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
    Tonelli A, D'Angelo MG, Salati R, Villa L, Germinasi C, Frattini T, Meola G, Turconi AC, Bresolin N, Bassi MT.
    J Neurol Sci; 2006 Feb 15; 241(1-2):13-7. PubMed ID: 16325861
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  • 9. [A case of spinocerebellar ataxia 6 accompanied with schizophrenia].
    Nakanishi I, Miwa H, Hayata T, Kawada A, Kondo T.
    No To Shinkei; 2004 Jan 15; 56(1):49-52. PubMed ID: 15024829
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  • 10. Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family.
    Alonso I, Barros J, Tuna A, Coelho J, Sequeiros J, Silveira I, Coutinho P.
    Arch Neurol; 2003 Apr 15; 60(4):610-4. PubMed ID: 12707077
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  • 11. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6.
    Yu GY, Howell MJ, Roller MJ, Xie TD, Gomez CM.
    Ann Neurol; 2005 Mar 15; 57(3):349-54. PubMed ID: 15732118
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  • 12. Genetics of the SCA6 gene in a large family segregating an autosomal dominant "pure" cerebellar ataxia.
    García-Planells J, Cuesta A, Vilchez JJ, Martínez F, Prieto F, Palau F.
    J Med Genet; 1999 Feb 15; 36(2):148-51. PubMed ID: 10051016
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  • 13. Positional vertigo and macroscopic downbeat positioning nystagmus in spinocerebellar ataxia type 6 (SCA6).
    Yabe I, Sasaki H, Takeichi N, Takei A, Hamada T, Fukushima K, Tashiro K.
    J Neurol; 2003 Apr 15; 250(4):440-3. PubMed ID: 12700909
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  • 14. Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
    Gomez CM, Thompson RM, Gammack JT, Perlman SL, Dobyns WB, Truwit CL, Zee DS, Clark HB, Anderson JH.
    Ann Neurol; 1997 Dec 15; 42(6):933-50. PubMed ID: 9403487
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  • 15. Possible reduced penetrance of expansion of 44 to 47 CAG/CAA repeats in the TATA-binding protein gene in spinocerebellar ataxia type 17.
    Oda M, Maruyama H, Komure O, Morino H, Terasawa H, Izumi Y, Imamura T, Yasuda M, Ichikawa K, Ogawa M, Matsumoto M, Kawakami H.
    Arch Neurol; 2004 Feb 15; 61(2):209-12. PubMed ID: 14967767
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  • 16. Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation.
    Zafeiriou DI, Lehmann-Horn F, Vargiami E, Teflioudi E, Ververi A, Jurkat-Rott K.
    Eur J Paediatr Neurol; 2009 Mar 15; 13(2):191-3. PubMed ID: 18602318
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