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Journal Abstract Search

313 related items for PubMed ID: 16124012

  • 1. Intrafamilial variability in fragile X-associated tremor/ataxia syndrome.
    Peters N, Kamm C, Asmus F, Holinski-Feder E, Kraft E, Dichgans M, Brüning R, Gasser T, Bötzel K.
    Mov Disord; 2006 Jan; 21(1):98-102. PubMed ID: 16124012
    [Abstract] [Full Text] [Related]

  • 2. Fragile X-associated tremor/ataxia syndrome: intrafamilial variability and the size of the FMR1 premutation CGG repeat.
    Capelli LP, Gonçalves MR, Kok F, Leite CC, Nitrini R, Barbosa ER, Vianna-Morgante AM.
    Mov Disord; 2007 Apr 30; 22(6):866-70. PubMed ID: 17290448
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  • 3. [Late cerebellar ataxia associated with fragile X premutation].
    Chaussenot A, Borg M, Bayreuther C, Lebrun C.
    Rev Neurol (Paris); 2008 Nov 30; 164(11):957-63. PubMed ID: 18808779
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  • 4. Premutations in the FMR1 gene are uncommon in men undergoing genetic testing for spinocerebellar ataxia.
    Adams SA, Steenblock KJ, Thibodeau SN, Lindor NM.
    J Neurogenet; 2008 Nov 30; 22(1):77-92. PubMed ID: 18363164
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  • 5. Tremor/ataxia syndrome and fragile X premutation: diagnostic caveats.
    Loesch DZ, Litewka L, Churchyard A, Gould E, Tassone F, Cook M.
    J Clin Neurosci; 2007 Mar 30; 14(3):245-8. PubMed ID: 17194594
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  • 6. Treatment of fragile-X-associated tremor/ataxia syndrome with deep brain stimulation.
    Ferrara JM, Adam OR, Ondo WG.
    Mov Disord; 2009 Jan 15; 24(1):149-51. PubMed ID: 18951504
    [No Abstract] [Full Text] [Related]

  • 7. FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy.
    Biancalana V, Toft M, Le Ber I, Tison F, Scherrer E, Thibodeau S, Mandel JL, Brice A, Farrer MJ, Dürr A.
    Arch Neurol; 2005 Jun 15; 62(6):962-6. PubMed ID: 15956167
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  • 8. [Progressive ataxia and cognitive deficits caused by premutation in the fragile-X-mental retardation gene].
    Roks G, Sistermans EA, de Vries LB, Nijssen PC.
    Ned Tijdschr Geneeskd; 2005 Oct 22; 149(43):2418-22. PubMed ID: 16277133
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  • 10. Initial diagnoses given to persons with the fragile X associated tremor/ataxia syndrome (FXTAS).
    Hall DA, Berry-Kravis E, Jacquemont S, Rice CD, Cogswell J, Zhang L, Hagerman RJ, Hagerman PJ, Leehey MA.
    Neurology; 2005 Jul 26; 65(2):299-301. PubMed ID: 16043804
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  • 12. Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond.
    Loesch DZ, Churchyard A, Brotchie P, Marot M, Tassone F.
    Clin Genet; 2005 May 26; 67(5):412-7. PubMed ID: 15811008
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  • 14. The fragile X tremor ataxia syndrome in the differential diagnosis of multiple system atrophy: data from the EMSA Study Group.
    Kamm C, Healy DG, Quinn NP, Wüllner U, Moller JC, Schols L, Geser F, Burk K, Børglum AD, Pellecchia MT, Tolosa E, del Sorbo F, Nilsson C, Bandmann O, Sharma M, Mayer P, Gasteiger M, Haworth A, Ozawa T, Lees AJ, Short J, Giunti P, Holinski-Feder E, Illig T, Wichmann HE, Wenning GK, Wood NW, Gasser T, European Multiple System Atrophy Study Group.
    Brain; 2005 Aug 26; 128(Pt 8):1855-60. PubMed ID: 15947063
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  • 15. Volumetric brain changes in females with fragile X-associated tremor/ataxia syndrome (FXTAS).
    Adams JS, Adams PE, Nguyen D, Brunberg JA, Tassone F, Zhang W, Koldewyn K, Rivera SM, Grigsby J, Zhang L, DeCarli C, Hagerman PJ, Hagerman RJ.
    Neurology; 2007 Aug 28; 69(9):851-9. PubMed ID: 17724287
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  • 17. A case of fragile X premutation tremor/ataxia syndrome with evidence of mitochondrial dysfunction.
    Rizzo G, Pizza F, Scaglione C, Tonon C, Lodi R, Barbiroli B, Ambrosetto P, Martinelli P.
    Mov Disord; 2006 Sep 28; 21(9):1541-2. PubMed ID: 16830323
    [No Abstract] [Full Text] [Related]

  • 18. A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes.
    Loesch DZ, Cook M, Litewka L, Gould E, Churchyard A, Tassone F, Slater HR, Storey E.
    J Med Genet; 2008 Mar 28; 45(3):179-81. PubMed ID: 18057083
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  • 20. The fragile X-associated tremor ataxia syndrome (FXTAS) in Indonesia.
    Winarni TI, Mundhofir FE, Ediati A, Belladona M, Nillesen WM, Yntema HG, Hamel BC, Faradz SM, Hagerman RJ.
    Clin Genet; 2013 Mar 28; 83(3):263-8. PubMed ID: 22568721
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