These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

238 related articles for article (PubMed ID: 24657309)

  • 1. Genetics of Huntington's disease and related disorders.
    Burgunder JM
    Drug Discov Today; 2014 Jul; 19(7):985-9. PubMed ID: 24657309
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hereditary chorea - what else to consider when the Huntington's disease genetics test is negative?
    Malek N; Newman EJ
    Acta Neurol Scand; 2017 Jan; 135(1):25-33. PubMed ID: 27150574
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Huntington disease and Huntington disease-like in a case series from Brazil.
    Castilhos RM; Souza AF; Furtado GV; Gheno TC; Silva AL; Vargas FR; Lima MA; Barsottini O; Pedroso JL; Godeiro C; Salarini D; Pereira ET; Lin K; Toralles MB; Saute JA; Rieder CR; Quintas M; Sequeiros J; Alonso I; Saraiva-Pereira ML; Jardim LB
    Clin Genet; 2014 Oct; 86(4):373-7. PubMed ID: 24102565
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Differential diagnosis of Huntington's disease: what the clinician should know.
    Cardoso F
    Neurodegener Dis Manag; 2014; 4(1):67-72. PubMed ID: 24640980
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Chorea and Huntington's disease].
    Dürr A
    Rev Prat; 1997 May; 47(10):1083-7. PubMed ID: 9208671
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Huntington's disease phenocopy syndromes.
    Wild EJ; Tabrizi SJ
    Curr Opin Neurol; 2007 Dec; 20(6):681-7. PubMed ID: 17992089
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Unusual variability of PRRT2 linked phenotypes within a family.
    Brueckner F; Kohl B; Puest B; Gassner S; Osseforth J; Lindenau M; Stodieck S; Biskup S; Lohmann E
    Eur J Paediatr Neurol; 2014 Jul; 18(4):540-2. PubMed ID: 24755245
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Huntington disease and other choreas.
    Cardoso F
    Neurol Clin; 2009 Aug; 27(3):719-36, vi. PubMed ID: 19555828
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Choreas, hereditary and other ataxias, tics, myoclonus, and other movement disorders.
    Tolosa E; Berciano J
    Curr Opin Neurol Neurosurg; 1993 Jun; 6(3):358-68. PubMed ID: 8507906
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutations in PRRT2 result in paroxysmal dyskinesias with marked variability in clinical expression.
    Liu Q; Qi Z; Wan XH; Li JY; Shi L; Lu Q; Zhou XQ; Qiao L; Wu LW; Liu XQ; Yang W; Liu Y; Cui LY; Zhang X
    J Med Genet; 2012 Feb; 49(2):79-82. PubMed ID: 22209761
    [TBL] [Abstract][Full Text] [Related]  

  • 11. PRRT2 mutations and paroxysmal disorders.
    Méneret A; Gaudebout C; Riant F; Vidailhet M; Depienne C; Roze E
    Eur J Neurol; 2013 Jun; 20(6):872-8. PubMed ID: 23398397
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The differential diagnosis of chorea.
    Wild EJ; Tabrizi SJ
    Pract Neurol; 2007 Nov; 7(6):360-73. PubMed ID: 18024776
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Early Diagnosis of Chorea-Acanthocytosis: Orofacial Dyskinesia, Epileptic Seizures, and HyperCKemia].
    Schneider C; Danek A; Hostmann A; Fink GR; Burghaus L
    Fortschr Neurol Psychiatr; 2017 May; 85(5):270-273. PubMed ID: 28561176
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test.
    Schneider SA; Walker RH; Bhatia KP
    Nat Clin Pract Neurol; 2007 Sep; 3(9):517-25. PubMed ID: 17805246
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Role of PRRT2 in common paroxysmal neurological disorders: a gene with remarkable pleiotropy.
    Heron SE; Dibbens LM
    J Med Genet; 2013 Mar; 50(3):133-9. PubMed ID: 23343561
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Huntington's disease and other choreas.
    Quinn N; Schrag A
    J Neurol; 1998 Nov; 245(11):709-16. PubMed ID: 9808238
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cause and course in a series of patients with sporadic chorea.
    Piccolo I; Defanti CA; Soliveri P; Volontè MA; Cislaghi G; Girotti F
    J Neurol; 2003 Apr; 250(4):429-35. PubMed ID: 12700907
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea.
    MacMillan JC; Morrison PJ; Nevin NC; Shaw DJ; Harper PS; Quarrell OW; Snell RG
    J Med Genet; 1993 Dec; 30(12):1012-3. PubMed ID: 8133497
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differential diagnosis of Huntington's disease- neurological aspects of NKX2-1-related disorders.
    Skwara J; Nowicki M; Sharif L; Milanowski Ł; Dulski J; Elert-Dobkowska E; Skrzypek K; Hoffman-Zacharska D; Koziorowski D; Sławek J
    J Neural Transm (Vienna); 2024 Sep; 131(9):1013-1024. PubMed ID: 38916623
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Current perspectives in the treatment of Huntington's chorea].
    Kuran W
    Neurol Neurochir Pol; 2002; 36(4):757-65. PubMed ID: 12418139
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.