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Journal Abstract Search


159 related items for PubMed ID: 11440772

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  • 6. Cognitive decline in Huntington's disease expansion gene carriers.
    Baake V, Reijntjes RHAM, Dumas EM, Thompson JC, REGISTRY Investigators of the European Huntington's Disease Network, Roos RAC.
    Cortex; 2017 Oct; 95():51-62. PubMed ID: 28843844
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  • 7. Psychiatric symptoms and CAG expansion in Huntington's disease.
    Weigell-Weber M, Schmid W, Spiegel R.
    Am J Med Genet; 1996 Feb 16; 67(1):53-7. PubMed ID: 8678115
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  • 9. Are cognitive changes the first symptoms of Huntington's disease? A study of gene carriers.
    Hahn-Barma V, Deweer B, Dürr A, Dodé C, Feingold J, Pillon B, Agid Y, Brice A, Dubois B.
    J Neurol Neurosurg Psychiatry; 1998 Feb 16; 64(2):172-7. PubMed ID: 9489526
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  • 10. Clinical and genetic characteristics in patients with Huntington's disease from China.
    Yang J, Chen K, Wei Q, Chen Y, Cao B, Burgunder JM, Shang HF.
    Neurol Res; 2016 Oct 16; 38(10):916-20. PubMed ID: 27483361
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  • 12. Prediction of manifest Huntington's disease with clinical and imaging measures: a prospective observational study.
    Paulsen JS, Long JD, Ross CA, Harrington DL, Erwin CJ, Williams JK, Westervelt HJ, Johnson HJ, Aylward EH, Zhang Y, Bockholt HJ, Barker RA, PREDICT-HD Investigators and Coordinators of the Huntington Study Group.
    Lancet Neurol; 2014 Dec 16; 13(12):1193-201. PubMed ID: 25453459
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  • 13. Beyond the CAG triplet number: exploring potential predictors of delayed age of onset in Huntington's disease.
    Di Tella S, Lo Monaco MR, Petracca M, Zinzi P, Solito M, Piano C, Calabresi P, Silveri MC, Bentivoglio AR.
    J Neurol; 2022 Dec 16; 269(12):6634-6640. PubMed ID: 35915275
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  • 14. Genetics of Huntington disease.
    Nance MA.
    Handb Clin Neurol; 2017 Dec 16; 144():3-14. PubMed ID: 28947123
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  • 15. Psychopathology in verified Huntington's disease gene carriers.
    van Duijn E, Kingma EM, van der Mast RC.
    J Neuropsychiatry Clin Neurosci; 2007 Dec 16; 19(4):441-8. PubMed ID: 18070848
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  • 16. Cognitive scores in carriers of Huntington's disease gene compared to noncarriers.
    Foroud T, Siemers E, Kleindorfer D, Bill DJ, Hodes ME, Norton JA, Conneally PM, Christian JC.
    Ann Neurol; 1995 May 16; 37(5):657-64. PubMed ID: 7755361
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  • 17. [Clinical and genetic study of juvenile form of Huntington's disease].
    Zdzienicka E, Rakowicz M, Mierzewska H, Hoffman-Zacharska D, Jakubowska T, Poniatowska R, Sułek A, Waliniowska E, Zalewska U, Kulczycki J, Zaremba J.
    Neurol Neurochir Pol; 2002 May 16; 36(2):245-58. PubMed ID: 12046502
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  • 18. Huntington's disease as caused by 34 CAG repeats.
    Andrich J, Arning L, Wieczorek S, Kraus PH, Gold R, Saft C.
    Mov Disord; 2008 Apr 30; 23(6):879-81. PubMed ID: 18307262
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  • 19. Severity of cognitive impairment in juvenile and late-onset Huntington disease.
    Gómez-Tortosa E, del Barrio A, García Ruiz PJ, Pernaute RS, Benítez J, Barroso A, Jiménez FJ, García Yébenes J.
    Arch Neurol; 1998 Jun 30; 55(6):835-43. PubMed ID: 9626775
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  • 20. Familial aggregation of psychotic symptoms in Huntington's disease.
    Tsuang D, Almqvist EW, Lipe H, Strgar F, DiGiacomo L, Hoff D, Eugenio C, Hayden MR, Bird TD.
    Am J Psychiatry; 2000 Dec 30; 157(12):1955-9. PubMed ID: 11097960
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