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 *

175 related articles for article (PubMed ID: 16512624)

  • 1. [Rapid-onset dystonia-parkinsonism].
    Zaremba J
    Przegl Lek; 2005; 62(11):1296-7. PubMed ID: 16512624
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rapid-onset dystonia-parkinsonism: a fourth family consistent with linkage to chromosome 19q13.
    Zaremba J; Mierzewska H; Lysiak Z; Kramer P; Ozelius LJ; Brashear A
    Mov Disord; 2004 Dec; 19(12):1506-10. PubMed ID: 15390049
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
    de Carvalho Aguiar P; Sweadner KJ; Penniston JT; Zaremba J; Liu L; Caton M; Linazasoro G; Borg M; Tijssen MA; Bressman SB; Dobyns WB; Brashear A; Ozelius LJ
    Neuron; 2004 Jul; 43(2):169-75. PubMed ID: 15260953
    [TBL] [Abstract][Full Text] [Related]  

  • 4. ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism.
    Lee JY; Gollamudi S; Ozelius LJ; Kim JY; Jeon BS
    Mov Disord; 2007 Sep; 22(12):1808-9. PubMed ID: 17595045
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Paying the price at the pump: dystonia from mutations in a Na+/K+ -ATPase.
    Cannon SC
    Neuron; 2004 Jul; 43(2):153-4. PubMed ID: 15260948
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.
    Brashear A; Dobyns WB; de Carvalho Aguiar P; Borg M; Frijns CJ; Gollamudi S; Green A; Guimaraes J; Haake BC; Klein C; Linazasoro G; Münchau A; Raymond D; Riley D; Saunders-Pullman R; Tijssen MA; Webb D; Zaremba J; Bressman SB; Ozelius LJ
    Brain; 2007 Mar; 130(Pt 3):828-35. PubMed ID: 17282997
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Refined linkage to the RDP/DYT12 locus on 19q13.2 and evaluation of GRIK5 as a candidate gene.
    Kamm C; Leung J; Joseph S; Dobyns WB; Brashear A; Breakefield XO; Ozelius LJ
    Mov Disord; 2004 Jul; 19(7):845-847. PubMed ID: 15254951
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Rapid-onset dystonia-parkinsonism: sporadic form].
    Romero-López J; Moreno-Carretero MJ; Escriche-Jaime D; Corredera-García E
    Rev Neurol; 2008 Dec 16-31; 47(12):638-40. PubMed ID: 19085880
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heterogeneity of presentation and outcome in the Irish rapid-onset dystonia-parkinsonism kindred.
    McKeon A; Ozelius LJ; Hardiman O; Greenway MJ; Pittock SJ
    Mov Disord; 2007 Jul; 22(9):1325-7. PubMed ID: 17516473
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family.
    Kabakci K; Isbruch K; Schilling K; Hedrich K; de Carvalho Aguiar P; Ozelius LJ; Kramer PL; Schwarz MH; Klein C
    J Neurol Neurosurg Psychiatry; 2005 Jun; 76(6):860-2. PubMed ID: 15897512
    [TBL] [Abstract][Full Text] [Related]  

  • 11. X-linked recessive dystonia parkinsonism (XDP; Lubag; DYT3).
    Singleton A; Hague S; Hernandez D
    Adv Neurol; 2004; 94():139-42. PubMed ID: 14509666
    [No Abstract]   [Full Text] [Related]  

  • 12. Dystonia-parkinsonism disease gene discovery: expect surprises.
    Hayflick SJ
    Ann Neurol; 2009 Jan; 65(1):2-3. PubMed ID: 19194873
    [No Abstract]   [Full Text] [Related]  

  • 13. Dystonia-plus syndromes.
    Asmus F; Gasser T
    Eur J Neurol; 2010 Jul; 17 Suppl 1():37-45. PubMed ID: 20590807
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Phenotypic and molecular analyses of X-linked dystonia-parkinsonism ("lubag") in women.
    Evidente VG; Nolte D; Niemann S; Advincula J; Mayo MC; Natividad FF; Müller U
    Arch Neurol; 2004 Dec; 61(12):1956-9. PubMed ID: 15596620
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.
    DeAndrade MP; Yokoi F; van Groen T; Lingrel JB; Li Y
    Behav Brain Res; 2011 Jan; 216(2):659-65. PubMed ID: 20850480
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Rapid-onset dystonia-parkinsonism with ATP1A3 mutation and left lower limb paroxysmal dystonia.
    Nomura S; Kashiwagi M; Tanabe T; Oba C; Yanagi K; Kaname T; Okamoto N; Ashida A
    Brain Dev; 2021 Apr; 43(4):566-570. PubMed ID: 33451880
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel family with an unusual early-onset generalized dystonia.
    Fabbrini G; Brancati F; Vacca L; Valente EM; Nemeth A; Meesaq A; Sykes N; Dallapiccola B; Berardelli A
    Mov Disord; 2005 Jan; 20(1):81-6. PubMed ID: 15390042
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cognitive impairment in rapid-onset dystonia-parkinsonism.
    Cook JF; Hill DF; Snively BM; Boggs N; Suerken CK; Haq I; Stacy M; McCall WV; Ozelius LJ; Sweadner KJ; Brashear A
    Mov Disord; 2014 Mar; 29(3):344-50. PubMed ID: 24436111
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ATP1A3 related disease manifesting as rapid onset dystonia-parkinsonism with prominent myoclonus and exaggerated startle.
    Williams L; Waller SE; Bradley M; Lockhart A; Narayanan RK; Kumar KR; Morales Briceno H; Tchan M; Healy DG; Fung VSC
    Parkinsonism Relat Disord; 2023 Dec; 117():105864. PubMed ID: 37827923
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism.
    Blanco-Arias P; Einholm AP; Mamsa H; Concheiro C; Gutiérrez-de-Terán H; Romero J; Toustrup-Jensen MS; Carracedo A; Jen JC; Vilsen B; Sobrido MJ
    Hum Mol Genet; 2009 Jul; 18(13):2370-7. PubMed ID: 19351654
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.