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 *

136 related articles for article (PubMed ID: 24783662)

  • 1. A newborn case of intestinal infarction with homozygous MTHFR C677T and heterozygous of factor V Leiden G1691A, PAL-1 4G/5G mutations.
    Sandal G; Duman L; Ayata A
    Genet Couns; 2014; 25(1):81-4. PubMed ID: 24783662
    [No Abstract]   [Full Text] [Related]  

  • 2. Two cousins with neonatal stroke, PAI-1 4G variant and MTHFR A1298C mutation.
    Golomb MR; Heiny M; Garg BP
    J Child Neurol; 2007 Jun; 22(6):753-5. PubMed ID: 17641264
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Significance of factor V, prothrombin, MTHFR, and PAI-1 genotypes in childhood cerebral thrombosis.
    Ozyurek E; Balta G; Degerliyurt A; Parlak H; Aysun S; Gürgey A
    Clin Appl Thromb Hemost; 2007 Apr; 13(2):154-60. PubMed ID: 17456624
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Contraception-related deep venous thrombosis and pulmonary embolism in a 17-Year-old girl heterozygous for factor V leiden, prothrombin G20210A mutation, MTHFR C677T and homozygous for PAI-1 mutation: report of a family with multiple genetic risk factors and review of the literature.
    Lenicek Krleza J; Jakovljevic G; Bronic A; Coen Herak D; Bonevski A; Stepan-Giljevic J; Roic G
    Pathophysiol Haemost Thromb; 2010; 37(1):24-9. PubMed ID: 20664190
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: the Linz Peripheral Arterial Disease (LIPAD) study.
    Mueller T; Marschon R; Dieplinger B; Haidinger D; Gegenhuber A; Poelz W; Webersinke G; Haltmayer M
    J Vasc Surg; 2005 May; 41(5):808-15. PubMed ID: 15886665
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.
    Yasa MH; Bolaman Z; Yukselen V; Kadikoylu G; Karaoglul AO; Batun S
    Hepatogastroenterology; 2007; 54(77):1438-42. PubMed ID: 17708272
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Mutations of genes associated with thromboses in ischemic stroke in patients with primary antiphospholipid syndrome].
    Kalashnikova LA; Dobrynina LA; Patrusheva NL; Kovalenko TF; Patrushev LI; Aleksandrova EN; Berkovskiĭ AL; Sergeeva EV; Nasonov EL
    Ter Arkh; 2005; 77(10):49-53. PubMed ID: 16320685
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Renal transplantation experience in a patient with factor V Leiden homozygous, MTHFR C677T heterozygous, and PAI heterozygous mutation.
    Gülhan B; Tavil B; Gümrük F; Aki TF; Topaloglu R
    Pediatr Transplant; 2015 Aug; 19(5):E126-9. PubMed ID: 25996881
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation of Factor V G1691A, prothrombin G20210A, Factor XIII V34L, MTHFR A1298C, MTHFR C677T and PAI-1 4G/5G genotype frequencies of patients subjected to cardiovascular disease (CVD) panel in south-east region of Turkey.
    Oztuzcu S; Ergun S; Ulaşlı M; Nacarkahya G; Iğci YZ; Iğci M; Bayraktar R; Tamer A; Çakmak EA; Arslan A
    Mol Biol Rep; 2014 Jun; 41(6):3671-6. PubMed ID: 24532105
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.
    Dölek B; Eraslan S; Eroğlu S; Kesim BE; Ulutin T; Yalçiner A; Laleli YR; Gözükirmizi N
    Clin Appl Thromb Hemost; 2007 Oct; 13(4):435-8. PubMed ID: 17911197
    [TBL] [Abstract][Full Text] [Related]  

  • 11. MTHFR C677T mutation, factor II G20210A mutation and factor V Leiden as risks factor for youth retinal vein occlusion.
    Cruciani F; Moramarco A; Curto T; Labate A; Recupero V; Conti L; Gandolfo GM; Balacco Gabrieli C
    Clin Ter; 2003; 154(5):299-303. PubMed ID: 14994919
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.
    Yenicesu GI; Cetin M; Ozdemir O; Cetin A; Ozen F; Yenicesu C; Yildiz C; Kocak N
    Am J Reprod Immunol; 2010 Feb; 63(2):126-36. PubMed ID: 19906129
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ABO blood group but not haemostasis genetic polymorphisms significantly influence thrombotic risk: a study of 180 homozygotes for the Factor V Leiden mutation.
    Procare-GEHT Group
    Br J Haematol; 2006 Dec; 135(5):697-702. PubMed ID: 17107352
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Do thrombophilic gene mutations have a role on thromboembolic events in cancer patients?
    Ozkan M; Sivgin S; Kocyigit I; Emirogullari F; Dikilitas M; Kaynar L; Ozkul Y; Er O
    Asia Pac J Clin Oncol; 2012 Sep; 8(3):e34-41. PubMed ID: 22898008
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Combined genetic mutations have remarkable effect on deep venous thrombosis and/or pulmonary embolism occurence.
    Simsek E; Yesilyurt A; Pinarli F; Eyerci N; Ulus AT
    Gene; 2014 Feb; 536(1):171-6. PubMed ID: 24334115
    [TBL] [Abstract][Full Text] [Related]  

  • 16. AXILLARY ARTERY THROMBOSIS IN A NEWBORN HOMOZYGOUS FOR METHYLENETETRAHYDROFOLATE REDUCTASE (A1298C) MUTATION AND HETEROZYGOUS FOR FACTOR V LEIDEN (G506A) MUTATION.
    Dilli D; Fettah N; Çinar HG; Özyazici E; Dursun A; Zenciroğlu A; Okumuş N
    Genet Couns; 2016; 27(1):87-9. PubMed ID: 27192896
    [No Abstract]   [Full Text] [Related]  

  • 17. Genetic polymorphisms associated with retinal vein occlusion: a Greek case-control study and meta-analysis.
    Yioti GG; Panagiotou OA; Vartholomatos GA; Kolaitis NI; Pappa CN; Evangelou E; Stefaniotou MI
    Ophthalmic Genet; 2013 Sep; 34(3):130-9. PubMed ID: 23289804
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Prevalence of thrombophilic mutations of FV Leiden, prothrombin G20210A and PAl-1 4G/5G and their combinations in a group of 1450 healthy middle-aged individuals in the Prague and Central Bohemian regions (results of FRET real-time PCR assay)].
    Kvasnicka J; Hájková J; Bobcíková P; Kvasnicka T; Dusková D; Poletínová S; Kieferová V
    Cas Lek Cesk; 2012; 151(2):76-82. PubMed ID: 22515013
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.
    Eid SS; Rihani G
    Clin Lab Sci; 2004; 17(4):200-2. PubMed ID: 15559724
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.