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 *

96 related articles for article (PubMed ID: 22339112)

  • 1. Myocardial infarction in a newborn heterozygous for the MTHFR C677T mutation.
    Clark AB; Stokes TA; Krous HF; Carbine DN
    Pediatr Dev Pathol; 2012; 15(3):232-6. PubMed ID: 22339112
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Tricuspid valve thrombus and pulmonary embolus in an infant with homozygous thermolabile methylenetetrahydrofolate reductase and heterozygous prothrombin G20210A variant.
    Thornburg CD; Lattimore KA; Pipe SW
    J Perinatol; 2003 Sep; 23(6):513-5. PubMed ID: 13679943
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Aortic thrombus and acute pulmonary embolism in an individual heterozygous for the MTHFR C677T mutation.
    D'Amato N; Correale M; D'Agostino C
    Rev Esp Cardiol; 2010 Nov; 63(11):1366. PubMed ID: 21070731
    [No Abstract]   [Full Text] [Related]  

  • 4. The methylenetetrahydrofolate reductase (MTHFR) 677C-->T mutation and cardiovascular risk--A case of ischemic stroke and acute myocardial infarction.
    Melo M; Gaspar E; Madeira S; de Moura P; Alexandrino B; de Moura JJ
    Rev Port Cardiol; 2005 Jan; 24(1):89-99. PubMed ID: 15773669
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Left main coronary artery thrombosis with distal coronary embolization in a patient with methyltetrahydrofolate reductase C677T mutation presenting with STEMI.
    Iaccarino D; Placentino F; Reggi A; Tondi S
    Minerva Cardioangiol; 2016 Dec; 64(6):711-713. PubMed ID: 27760988
    [No Abstract]   [Full Text] [Related]  

  • 6. Thrombophilia in young patients with acute myocardial infarction.
    Celik M; Altintas A; Celik Y; Karabulut A; Ayyildiz O
    Saudi Med J; 2008 Jan; 29(1):48-54. PubMed ID: 18176672
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Case report: Acute myocardial infarction in a 32-year-old white male found to have antiphospholipid antibody syndrome and MTHFR mutation homozygosity.
    Stoupakis G; Bejjanki R; Arora R
    Heart Lung; 2003; 32(4):266-71. PubMed ID: 12891167
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 84(9):824-8. PubMed ID: 10477457
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Myocardial infarction and venous thrombosis in a 42-year old woman with heterozygous methylenetetrahydrofolate reductase (MTHRF) gene mutation, hyperhomocysteinemia, and protein C deficiency.
    Cakir O; Ayyildiz O; Goz M; Sit D; Eren N
    Int J Cardiol; 2007 May; 117(3):e98-100. PubMed ID: 17360059
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MTHFR C677T polymorphism and its relationship to myocardial infarction in the Eastern Black Sea region of Turkey.
    Uçar F; Celik S; Yücel B; Sönmez M; Celep F; Erkut N
    Arch Med Res; 2011 Nov; 42(8):709-12. PubMed ID: 22222489
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Arterial thrombosis and acute myocardial infarction with angiographically normal coronary arteries in a woman heterozygous for both factor V Leiden and prothrombin mutation.
    Gaspar J; Benchimol C; Gadelha T; Penna GL
    Rev Port Cardiol; 2011 Sep; 30(9):727-9. PubMed ID: 21958997
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene among the Lebanese population.
    Almawi WY; Finan RR; Tamim H; Daccache JL; Irani-Hakime N
    Am J Hematol; 2004 May; 76(1):85-7. PubMed ID: 15114606
    [TBL] [Abstract][Full Text] [Related]  

  • 13. C677T polymorphism of the 5,10 MTHFR gene in young Mexican subjects with ST-elevation myocardial infarction.
    Isordia-Salas I; Trejo-Aguilar A; Valadés-Mejía MG; Santiago-Germán D; Leaños-Miranda A; Mendoza-Valdéz L; Jáuregui-Aguilar R; Borrayo-Sánchez G; Majluf-Cruz A
    Arch Med Res; 2010 May; 41(4):246-50. PubMed ID: 20637366
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.
    Kim RJ; Becker RC
    Am Heart J; 2003 Dec; 146(6):948-57. PubMed ID: 14660985
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The methylenetetrahydrofolate reductase gene polymorphism (C677T) is associated with increased cardiovascular mortality in Hungary.
    Kalina A; Czeizel AE
    Int J Cardiol; 2004 Nov; 97(2):333-4. PubMed ID: 15458711
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MTHFR homozygous mutation and additional risk factors for cerebral infarction in a large Italian family.
    Del Balzo F; Spalice A; Perla M; Properzi E; Iannetti P
    Pediatr Neurol; 2009 Jan; 40(1):63-7. PubMed ID: 19068258
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Factor V G1691A, apo E4 allele, hyperhomocysteinemia and MTHFR C677T in a young patient with myocardial infarction.
    Assanelli D; Ferrari R; Bollani G; Ettori F; Bonetti P; Bersatti F; Archetti S; Ruggeri G; Bonanome A; Martini G
    Thromb Haemost; 1999 Sep; 82(3):1196. PubMed ID: 10494787
    [No Abstract]   [Full Text] [Related]  

  • 18. Dynamic regulation of MTHFR mRNA expression and C677T genotype modulate mortality in coronary artery disease patients after revascularization.
    Pereira AC; Miyakawa AA; Lopes NH; Soares PR; de Oliveira SA; Cesar LA; Ramires JF; Hueb W; Krieger JE
    Thromb Res; 2007; 121(1):25-32. PubMed ID: 17604826
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Perinatal myocardial infarction in a newborn with a structurally normal heart.
    Muraskas J; Besinger R; Bell T; DeLeon S; Husain A
    Am J Perinatol; 1997 Feb; 14(2):93-7. PubMed ID: 9259906
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carrier-state of D allele in ACE gene insertion/deletion polymorphism is associated with coronary artery disease, in contrast to the C677-->T transition in the MTHFR gene.
    Zak I; Niemiec P; Sarecka B; Balcerzyk A; Ciemniewski Z; Rudowska E; Dylag S
    Acta Biochim Pol; 2003; 50(2):527-34. PubMed ID: 12833177
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.