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Journal Abstract Search

125 related items for PubMed ID: 24496700

  • 1. PITX3 variants in Chinese patients with Parkinson's disease.
    Sand PG, Welz T.
    Swiss Med Wkly; 2014 Feb 04; 144():w13702. PubMed ID: 24496700
    [No Abstract] [Full Text] [Related]

  • 2. A novel synonymous SNP in PITX3 is associated with Parkinson's disease in Chinese population.
    Gui Y, Zhao Y, Liu H, Fu J, Xu Z, Hu X.
    Swiss Med Wkly; 2012 Feb 04; 142():w13521. PubMed ID: 22411443
    [Abstract] [Full Text] [Related]

  • 3. PITX3 polymorphism is not associated with Parkinson's disease in a Chinese population.
    Cai Y, Ding H, Gu Z, Baskys A, Ma J, Chan P.
    Neurosci Lett; 2011 Nov 21; 505(3):260-2. PubMed ID: 22037506
    [Abstract] [Full Text] [Related]

  • 4. PITX3 gene polymorphism is associated with Parkinson's disease in Chinese population.
    Liu J, Sun QY, Tang BS, Hu L, Yu RH, Wang L, Shi CH, Yan XX, Pan Q, Xia K, Guo JF.
    Brain Res; 2011 May 25; 1392():116-20. PubMed ID: 21524731
    [Abstract] [Full Text] [Related]

  • 5. The transcription factor Pitx3 is a risk modifier for Parkinson's disease in a Chinese Han population.
    Yu LH, Lin ZF, Liu Y, Hu FY, He XH, Liu ZL, Xu YM.
    Eur J Neurol; 2011 May 25; 18(5):778-83. PubMed ID: 21138504
    [Abstract] [Full Text] [Related]

  • 6. PITX3 and risk for Parkinson's disease: a systematic review and meta-analysis.
    Jiménez-Jiménez FJ, García-Martín E, Alonso-Navarro H, Agúndez JA.
    Eur Neurol; 2014 May 25; 71(1-2):49-56. PubMed ID: 24525476
    [Abstract] [Full Text] [Related]

  • 7. Systematic genetic analysis of the PITX3 gene in patients with Parkinson disease.
    Guo Y, Le WD, Jankovic J, Yang HR, Xu HB, Xie WJ, Song Z, Deng H.
    Mov Disord; 2011 Aug 01; 26(9):1729-32. PubMed ID: 21469209
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  • 9. Association between PITX3 promoter polymorphism and risk of Parkinson's disease: the impact of ethnicity and onset age.
    Qiu G, Fu C, Liang GH.
    Neurosci Lett; 2014 Feb 21; 561():128-33. PubMed ID: 24394914
    [Abstract] [Full Text] [Related]

  • 10. Association of transcription factor polymorphisms PITX3 and EN1 with Parkinson's disease.
    Haubenberger D, Reinthaler E, Mueller JC, Pirker W, Katzenschlager R, Froehlich R, Bruecke T, Daniel G, Auff E, Zimprich A.
    Neurobiol Aging; 2011 Feb 21; 32(2):302-7. PubMed ID: 19345444
    [Abstract] [Full Text] [Related]

  • 11. Genetic variants of the PITX3 gene are not associated with late-onset sporadic Parkinson's disease in a Chinese population.
    Cai Y, Ding H, Gu Z, Ma J, Chan P.
    Neurosci Lett; 2011 Jul 08; 498(2):124-6. PubMed ID: 21565251
    [Abstract] [Full Text] [Related]

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  • 13. The transcription factor PITX3 is associated with sporadic Parkinson's disease.
    Fuchs J, Mueller JC, Lichtner P, Schulte C, Munz M, Berg D, Wüllner U, Illig T, Sharma M, Gasser T.
    Neurobiol Aging; 2009 May 08; 30(5):731-8. PubMed ID: 17905480
    [Abstract] [Full Text] [Related]

  • 14. PITX3 genotype and risk of dementia in Parkinson's disease: A population-based study.
    Bäckström D, Domellöf ME, Granåsen G, Linder J, Mayans S, Elgh E, Mo SJ, Forsgren L.
    J Neurol Sci; 2017 Oct 15; 381():278-284. PubMed ID: 28991698
    [Abstract] [Full Text] [Related]

  • 15. Analysis of the Micro-RNA-133 and PITX3 genes in Parkinson's disease.
    de Mena L, Coto E, Cardo LF, Díaz M, Blázquez M, Ribacoba R, Salvador C, Pastor P, Samaranch L, Moris G, Menéndez M, Corao AI, Alvarez V.
    Am J Med Genet B Neuropsychiatr Genet; 2010 Sep 15; 153B(6):1234-9. PubMed ID: 20468068
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  • 18. PITX3 polymorphism is associated with early onset Parkinson's disease.
    Bergman O, Håkansson A, Westberg L, Nordenström K, Carmine Belin A, Sydow O, Olson L, Holmberg B, Eriksson E, Nissbrandt H.
    Neurobiol Aging; 2010 Jan 15; 31(1):114-7. PubMed ID: 18420308
    [Abstract] [Full Text] [Related]

  • 19. No association of PARK10 polymorphism with Parkinson's disease in Han Chinese population.
    Tian S, Yang X, Zhao Q, Zheng J, Huang H, Chen Y, An R, Xu Y.
    Parkinsonism Relat Disord; 2017 Sep 15; 42():105-106. PubMed ID: 28651751
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