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 *

288 related articles for article (PubMed ID: 21370272)

  • 1. Movement disorders in spinocerebellar ataxias.
    van Gaalen J; Giunti P; van de Warrenburg BP
    Mov Disord; 2011 Apr; 26(5):792-800. PubMed ID: 21370272
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spinocerebellar ataxia type 2 (SCA2): clinical features and genetic analysis.
    Mutesa L; Pierquin G; Segers K; Vanbellinghen JF; Gahimbare L; Bours V
    J Trop Pediatr; 2008 Oct; 54(5):350-2. PubMed ID: 18499737
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Should spinocerebellar ataxias be included in the differential diagnosis for Huntington's diseases-like syndromes?
    Pedroso JL; de Freitas ME; Albuquerque MV; Saraiva-Pereira ML; Jardim LB; Barsottini OG
    J Neurol Sci; 2014 Dec; 347(1-2):356-8. PubMed ID: 25456461
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Brain pathology of spinocerebellar ataxias.
    Seidel K; Siswanto S; Brunt ER; den Dunnen W; Korf HW; Rüb U
    Acta Neuropathol; 2012 Jul; 124(1):1-21. PubMed ID: 22684686
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).
    Rolfs A; Koeppen AH; Bauer I; Bauer P; Buhlmann S; Topka H; Schöls L; Riess O
    Ann Neurol; 2003 Sep; 54(3):367-75. PubMed ID: 12953269
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Movement disorders in spinocerebellar ataxias in a cohort of Brazilian patients.
    Moro A; Munhoz RP; Moscovich M; Arruda WO; Raskin S; Teive HA
    Eur Neurol; 2014; 72(5-6):360-2. PubMed ID: 25322786
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 61(2):209-12. PubMed ID: 14967767
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Myoclonus-dystonia and spinocerebellar ataxia type 14 presenting with similar phenotypes: trunk tremor, myoclonus, and dystonia.
    Foncke EM; Beukers RJ; Tijssen CC; Koelman JH; Tijssen MA
    Parkinsonism Relat Disord; 2010 May; 16(4):288-9. PubMed ID: 19913450
    [TBL] [Abstract][Full Text] [Related]  

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

  • 11. Climbing fibers in spinocerebellar ataxia: A mechanism for the loss of motor control.
    Smeets CJ; Verbeek DS
    Neurobiol Dis; 2016 Apr; 88():96-106. PubMed ID: 26792399
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Non-motor and Extracerebellar Features in Spinocerebellar Ataxia Type 2.
    Pedroso JL; Braga-Neto P; Escorcio-Bezerra ML; Abrahão A; de Albuquerque MV; Filho FM; de Souza PV; de Rezende Pinto WB; Borges FR; Saraiva-Pereira ML; Jardim LB; Barsottini OG
    Cerebellum; 2017 Feb; 16(1):34-39. PubMed ID: 26825292
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Eye movement changes in autosomal dominant spinocerebellar ataxias.
    Rosini F; Pretegiani E; Battisti C; Dotti MT; Federico A; Rufa A
    Neurol Sci; 2020 Jul; 41(7):1719-1734. PubMed ID: 32130555
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Parkinsonism in spinocerebellar ataxia.
    Park H; Kim HJ; Jeon BS
    Biomed Res Int; 2015; 2015():125273. PubMed ID: 25866756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Speech in spinocerebellar ataxia.
    Schalling E; Hartelius L
    Brain Lang; 2013 Dec; 127(3):317-22. PubMed ID: 24182841
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Early onset autosomal dominant spinocerebellar ataxia with miosis: four cases.
    Timby N; Stattin EL; Kristiansen I; Eriksson U; Erikson A
    Eur J Paediatr Neurol; 2008 Jan; 12(1):38-40. PubMed ID: 17584505
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia?
    Kuoppamäki M; Giunti P; Quinn N; Wood NW; Bhatia KP
    Mov Disord; 2003 Feb; 18(2):200-6. PubMed ID: 12539216
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Movement Disorders in Autosomal Dominant Cerebellar Ataxias: A Systematic Review.
    Rossi M; Perez-Lloret S; Cerquetti D; Merello M
    Mov Disord Clin Pract; 2014 Sep; 1(3):154-160. PubMed ID: 30363920
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Should genetic testing for SCAs be included in the diagnostic workup for MSA?
    Kim HJ; Jeon BS; Shin J; Lee WW; Park H; Jung YJ; Ehm G
    Neurology; 2014 Nov; 83(19):1733-8. PubMed ID: 25298309
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.