BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

238 related articles for article (PubMed ID: 24803225)

  • 1. Rapid-onset dystonia-parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropathologic and neuroanatomical study of four siblings.
    Oblak AL; Hagen MC; Sweadner KJ; Haq I; Whitlow CT; Maldjian JA; Epperson F; Cook JF; Stacy M; Murrell JR; Ozelius LJ; Brashear A; Ghetti B
    Acta Neuropathol; 2014 Jul; 128(1):81-98. PubMed ID: 24803225
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [A childhood-onset rapid-onset dystonia parkinsonism family with ATP1A3 gene mutation and literatures review].
    Zhang CL; Yin F; He F; Gai N; Shi ZQ; Peng J
    Zhonghua Er Ke Za Zhi; 2017 Apr; 55(4):288-293. PubMed ID: 28441826
    [No Abstract]   [Full Text] [Related]  

  • 3. The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, Alternating Hemiplegia of Childhood, Rapid-onset Dystonia-Parkinsonism, CAPOS and beyond.
    Sweney MT; Newcomb TM; Swoboda KJ
    Pediatr Neurol; 2015 Jan; 52(1):56-64. PubMed ID: 25447930
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism ATP1A3 mutations reveals functional deficits, which do not correlate with disease severity.
    Lazarov E; Hillebrand M; Schröder S; Ternka K; Hofhuis J; Ohlenbusch A; Barrantes-Freer A; Pardo LA; Fruergaard MU; Nissen P; Brockmann K; Gärtner J; Rosewich H
    Neurobiol Dis; 2020 Sep; 143():105012. PubMed ID: 32653672
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A novel ATP1A3 mutation with unique clinical presentation.
    Rosewich H; Baethmann M; Ohlenbusch A; Gärtner J; Brockmann K
    J Neurol Sci; 2014 Jun; 341(1-2):133-5. PubMed ID: 24713507
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identical ATP1A3 mutation causes alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism phenotypes.
    Boelman C; Lagman-Bartolome AM; MacGregor DL; McCabe J; Logan WJ; Minassian BA
    Pediatr Neurol; 2014 Dec; 51(6):850-3. PubMed ID: 25439493
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Genome sequencing identifies a novel mutation in ATP1A3 in a family with dystonia in females only.
    Wilcox R; Brænne I; Brüggemann N; Winkler S; Wiegers K; Bertram L; Anderson T; Lohmann K
    J Neurol; 2015 Jan; 262(1):187-93. PubMed ID: 25359261
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heterozygous mice deficient in Atp1a3 exhibit motor deficits by chronic restraint stress.
    Sugimoto H; Ikeda K; Kawakami K
    Behav Brain Res; 2014 Oct; 272():100-10. PubMed ID: 24983657
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Revising rapid-onset dystonia-parkinsonism: Broadening indications for ATP1A3 testing.
    Haq IU; Snively BM; Sweadner KJ; Suerken CK; Cook JF; Ozelius LJ; Miller C; McCall WV; Whitlow CT; Brashear A
    Mov Disord; 2019 Oct; 34(10):1528-1536. PubMed ID: 31361359
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.
    Wei W; Zheng XF; Ruan DD; Gan YM; Zhang YP; Chen Y; Lin XF; Tang FQ; Luo JW; Li YF
    Neurol Sci; 2022 Apr; 43(4):2555-2563. PubMed ID: 34783933
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. The expanding clinical and genetic spectrum of ATP1A3-related disorders.
    Rosewich H; Ohlenbusch A; Huppke P; Schlotawa L; Baethmann M; Carrilho I; Fiori S; Lourenço CM; Sawyer S; Steinfeld R; Gärtner J; Brockmann K
    Neurology; 2014 Mar; 82(11):945-55. PubMed ID: 24523486
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Expanding Phenotypic Spectrums Associated with ATP1A3 Mutation in a Family with Rapid-Onset Dystonia Parkinsonism.
    Yuan Y; Ran L; Lei L; Zhu H; Zhu X; Chen H
    Neurodegener Dis; 2020; 20(2-3):84-89. PubMed ID: 33326973
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. ATP1A3-related disorders: An update.
    Carecchio M; Zorzi G; Ragona F; Zibordi F; Nardocci N
    Eur J Paediatr Neurol; 2018 Mar; 22(2):257-263. PubMed ID: 29291920
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases.
    Boonsimma P; Michael Gasser M; Netbaramee W; Wechapinan T; Srichomthong C; Ittiwut C; Wagner M; Krenn M; Zimprich F; Abicht A; Biskup S; Roser T; Borggraefe I; Suphapeetiporn K; Shotelersuk V
    Gene; 2020 Jul; 749():144709. PubMed ID: 32339621
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.
    Rosewich H; Thiele H; Ohlenbusch A; Maschke U; Altmüller J; Frommolt P; Zirn B; Ebinger F; Siemes H; Nürnberg P; Brockmann K; Gärtner J
    Lancet Neurol; 2012 Sep; 11(9):764-73. PubMed ID: 22850527
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mosaicism in ATP1A3-related disorders: not just a theoretical risk.
    Hully M; Ropars J; Hubert L; Boddaert N; Rio M; Bernardelli M; Desguerre I; Cormier-Daire V; Munnich A; de Lonlay P; Reilly L; Besmond C; Bahi-Buisson N
    Neurogenetics; 2017 Jan; 18(1):23-28. PubMed ID: 27726050
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.