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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

402 related items for PubMed ID: 19157768

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. Higher incidence of C677T polymorphism of the MTHFR gene in North Indian patients with vascular disease.
    Bhargava S, Ali A, Parakh R, Saxena R, Srivastava LM.
    Vascular; 2012 Apr; 20(2):88-95. PubMed ID: 22375042
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease.
    Kadziela J, Janas J, Dzielińska Z, Szperl M, Gaździk D, Chotkowska E, Piotrowski W, Ruzyłło W.
    Kardiol Pol; 2003 Jul; 59(7):17-26; discussion 26. PubMed ID: 14560345
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. 5,10-methylenetetrahydrofolate reductase C677T gene polymorphism and peripheral arterial disease: A meta-analysis.
    Liu F, Du J, Nie M, Fu J, Sun J.
    Vascular; 2021 Dec; 29(6):913-919. PubMed ID: 33357155
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Methylenetetrahydrofolate reductase C677T variant and hyperhomocysteinemia in subarachnoid hemorrhage patients from India.
    Kumar M, Goudihalli S, Mukherjee K, Dhandapani S, Sandhir R.
    Metab Brain Dis; 2018 Oct; 33(5):1617-1624. PubMed ID: 29926428
    [Abstract] [Full Text] [Related]

  • 11. 5,10-Methylenetetrahydrofolate reductase C677T gene polymorphism in Behcet's patients with or without ocular involvement.
    Ozkul Y, Evereklioglu C, Borlu M, Taheri S, Calis M, Dündar M, Ilhan O.
    Br J Ophthalmol; 2005 Dec; 89(12):1634-7. PubMed ID: 16299146
    [Abstract] [Full Text] [Related]

  • 12. Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and variations of homocysteine concentrations in patients with Behcet's disease.
    Messedi M, Frigui M, Chaabouni Kh, Turki M, Neifer M, Lahiyani A, Messaouad M, Bahloul Z, Ayedi F, Jamoussi K.
    Gene; 2013 Sep 15; 527(1):306-10. PubMed ID: 23827456
    [Abstract] [Full Text] [Related]

  • 13. The methylenetetrahydrofolate reductase C677T gene mutation is associated with hyperhomocysteinemia, cardiovascular disease and plasma B-type natriuretic peptide levels in Korea.
    Cho SE, Hong KS, Shin GJ, Chung WS.
    Clin Chem Lab Med; 2006 Sep 15; 44(9):1070-5. PubMed ID: 16958597
    [Abstract] [Full Text] [Related]

  • 14. Methylenetetrahydrofolate reductase gene polymorphism, homocysteine and risk of macroangiopathy in Type 2 diabetes mellitus.
    Sun J, Xu Y, Zhu Y, Lu H.
    J Endocrinol Invest; 2006 Oct 15; 29(9):814-20. PubMed ID: 17114913
    [Abstract] [Full Text] [Related]

  • 15. C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients.
    Gemmati D, Serino ML, Trivellato C, Fiorini S, Scapoli GL.
    Haematologica; 1999 Sep 15; 84(9):824-8. PubMed ID: 10477457
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. The role of methylenetetrahydrofolate reductase C677T gene polymorphism as a risk factor for coronary artery disease: a cross-sectional study in the Sidoarjo Regional General Hospital.
    Sugijo H, Sargowo D, Widjajanto E, Romdoni R.
    Pan Afr Med J; 2022 Sep 15; 41():212. PubMed ID: 35721657
    [Abstract] [Full Text] [Related]

  • 18. Association study of methylenetetrahydrofolate reductase C677T mutation with cerebral venous thrombosis in an Iranian population.
    Ghaznavi H, Soheili Z, Samiei S, Soltanpour MS.
    Blood Coagul Fibrinolysis; 2015 Dec 15; 26(8):869-73. PubMed ID: 26083986
    [Abstract] [Full Text] [Related]

  • 19. TT genotype of the methylenetetrahydrofolate reductase C677T polymorphism is an important determinant for homocysteine levels in multi-ethnic Malaysian ischaemic stroke patients.
    Mejia Mohamed EH, Tan KS, Ali JM, Mohamed Z.
    Ann Acad Med Singap; 2011 Apr 15; 40(4):186-91. PubMed ID: 21678004
    [Abstract] [Full Text] [Related]

  • 20. Association between MTHFR C677T Gene Polymorphisms and the Efficacy of Vitamin Therapy in lowering Homocysteine Levels among Stroke Patients with Hyperhomocysteinemia.
    Li ZC, Huang M, Yao QY, Lin CH, Hong BC, Wang JH, Zhang Z.
    J Integr Neurosci; 2024 Jan 10; 23(1):3. PubMed ID: 38287840
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 21.