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PUBMED FOR HANDHELDS

Journal Abstract Search


955 related items for PubMed ID: 32712352

  • 1. Association between epidermal growth factor receptor gene polymorphisms and susceptibility to Parkinson's disease.
    Jin J, Xue L, Bai X, Zhang X, Tian Q, Xie A.
    Neurosci Lett; 2020 Sep 25; 736():135273. PubMed ID: 32712352
    [Abstract] [Full Text] [Related]

  • 2. Association between ABCA7 gene polymorphisms and Parkinson's disease susceptibility in a northern Chinese Han population.
    Yang Z, Xue L, Li C, Li M, Xie A.
    Neurosci Lett; 2022 Jul 27; 784():136734. PubMed ID: 35709878
    [Abstract] [Full Text] [Related]

  • 3. Evaluation of the relationship between SORL1 gene polymorphism and Parkinson's disease in the Chinese population.
    Wang Y, Luan M, Xue L, Jin J, Xie A.
    Neurosci Lett; 2022 May 01; 778():136602. PubMed ID: 35364126
    [Abstract] [Full Text] [Related]

  • 4. CD33 polymorphisms and Parkinson's disease Parkinson's disease in northern Chinese Han population: A case-control study.
    Tian Q, Sun X, Li C, Yang Y, Hou B, Xie A.
    Neurosci Lett; 2023 Aug 24; 812():137400. PubMed ID: 37479176
    [Abstract] [Full Text] [Related]

  • 5. Association of VEGF gene polymorphisms with sporadic Parkinson's disease in Chinese Han population.
    Wu Y, Zhang Y, Han X, Li X, Xue L, Xie A.
    Neurol Sci; 2016 Dec 24; 37(12):1923-1929. PubMed ID: 27481110
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  • 7. The Impact of EGFR Gene Polymorphisms on the Risk of Alzheimer's Disease in a Chinese Han Population: A Case-Controlled Study.
    Chen X, Wang C, Zhou S, Li X, Wu L.
    Med Sci Monit; 2018 Jul 20; 24():5035-5040. PubMed ID: 30026459
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  • 8. Association between nucleotide-binding oligomerization domain protein 2 (NOD2) gene polymorphisms and Parkinson's disease (PD) susceptibility.
    Xu M, Zhang S, Zhao H, Ma C, Pan Y.
    Artif Cells Nanomed Biotechnol; 2019 Dec 20; 47(1):2134-2138. PubMed ID: 31146602
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  • 11. Association between NEK1 gene polymorphisms and the potential risk of sporadic Parkinson's disease in the Chinese Northern Han population: A case-control study.
    He Q, Zhou Y, Jin J, Tian Q, Li H, Hou B, Xie A.
    Neurosci Lett; 2024 Aug 10; 837():137913. PubMed ID: 39032803
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  • 13. SNCA rs3822086 C>T Polymorphism Increases the Susceptibility to Parkinson's Disease in a Chinese Han Population.
    Jian CD, Huang JM, Meng LQ, Li XB, Huang RY, Shi SL, Wu Y, Qin C, Chen J, Zhang YM, Wang S, Feng YL, Zhou SN.
    Genet Test Mol Biomarkers; 2015 Sep 10; 19(9):481-7. PubMed ID: 26203864
    [Abstract] [Full Text] [Related]

  • 14. The association between TLR3 rs3775290 polymorphism and sporadic Parkinson's disease in Chinese Han population.
    Wang J, Liu Y, Liu Y, Zhu K, Xie A.
    Neurosci Lett; 2020 May 29; 728():135005. PubMed ID: 32335220
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  • 16. Association of TLR4 gene polymorphisms with sporadic Parkinson's disease in a Han Chinese population.
    Zhao J, Han X, Xue L, Zhu K, Liu H, Xie A.
    Neurol Sci; 2015 Sep 29; 36(9):1659-65. PubMed ID: 25908385
    [Abstract] [Full Text] [Related]

  • 17. Association between plasminogen activator inhibitor-1 gene polymorphisms and susceptibility to Parkinson's disease in Chinese patients.
    Xu Q, Lai Q, Wang J, Zhuang L, Cheng L, Mo Y, Liu L, Zhao Z, Zhang Y, Weng S, Qiao S.
    Acta Neurol Belg; 2022 Dec 29; 122(6):1557-1566. PubMed ID: 34845645
    [Abstract] [Full Text] [Related]

  • 18. Association of AKT1 gene polymorphisms with sporadic Parkinson's disease in Chinese Han population.
    Li XY, Teng JJ, Liu Y, Wu YB, Zheng Y, Xie AM.
    Neurosci Lett; 2016 Aug 26; 629():38-42. PubMed ID: 27353512
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  • 19. Association analysis of NUCKS1 and INPP5K polymorphism with Parkinson's disease.
    Zhu W, Luo X, Adnan A, Yu P, Zhang S, Huo Z, Xu Q, Pang H.
    Genes Genet Syst; 2018 Sep 15; 93(2):59-64. PubMed ID: 29607885
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  • 20. Single nucleotide polymorphisms in the toll-like receptor 2 (TLR2) gene are associated with sporadic Parkinson's disease in the North-eastern Han Chinese population.
    Li X, Xue L, Sun J, Sun Y, Xie A.
    Neurosci Lett; 2017 Aug 24; 656():72-76. PubMed ID: 28729076
    [Abstract] [Full Text] [Related]


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