137 related articles for article (PubMed ID: 9609246)
1. Multiplex ASA PCR for a simultaneous determination of factor V Leiden gene, G-->A 20210 prothrombin gene and C-->T 677 MTHFR gene mutations.
Hézard N; Cornillet-Lefebvre P; Gillot L; Potron G; Nguyen P
Thromb Haemost; 1998 May; 79(5):1054-5. PubMed ID: 9609246
[No Abstract] [Full Text] [Related]
2. Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR.
Hessner MJ; Luhm RA; Pearson SL; Endean DJ; Friedman KD; Montgomery RR
Thromb Haemost; 1999 May; 81(5):733-8. PubMed ID: 10365746
[TBL] [Abstract][Full Text] [Related]
3. Placental genotyping of the factor V Leiden, prothrombin 20210A and the methylenetetrahydrofolate reductase (MTHFR) C677T alleles in IUGR pregnancies.
Wisotzkey JD; Bayliss P; Rutherford E; Bell T
Thromb Haemost; 1999 May; 81(5):844-5. PubMed ID: 10365762
[No Abstract] [Full Text] [Related]
4. Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.
Toydemir PB; Elhan AH; Tükün A; Toydemir R; Gürler A; Tüzüner A; Bökesoy I
J Rheumatol; 2000 Dec; 27(12):2849-54. PubMed ID: 11128675
[TBL] [Abstract][Full Text] [Related]
5. Primer-engineered multiplex PCR-RFLP for detection of MTHFR C677T, prothrombin G20210A and factor V Leiden mutations.
Koksal V; Baris I; Etlik O
Exp Mol Pathol; 2007 Aug; 83(1):1-3. PubMed ID: 17275807
[TBL] [Abstract][Full Text] [Related]
6. A boy with venous thrombosis, homozygous for factor V Leiden, prothrombin G20210A and MTHFR C667t mutations, but belonging to an asymptomatic family.
Soria JM; Quintana R; Vallvé C; Iruin G; Cortés C; Fontcuberta J
Haematologica; 2000 Nov; 85(11):1230-2. PubMed ID: 11064483
[No Abstract] [Full Text] [Related]
7. Evaluation of the interactions of common genetic mutations in stroke subtypes.
Szolnoki Z; Somogyvári F; Kondacs A; Szabó M; Fodor L
J Neurol; 2002 Oct; 249(10):1391-7. PubMed ID: 12382154
[TBL] [Abstract][Full Text] [Related]
8. Factor V Leiden (G1691A), the prothrombin 3'-untranslated region variant (G20210A) and thermolabile methylenetetrahydrofolate reductase (C677T): a single genetic test genotypes all three loci--determination of frequencies in the S. Wales population of the UK.
Bowen DJ; Bowley S; John M; Collins PW
Thromb Haemost; 1998 May; 79(5):949-54. PubMed ID: 9609227
[TBL] [Abstract][Full Text] [Related]
9. Rapid automated simultaneous screening of (G1691A) Factor V, (G20210A) prothrombin, and (C677T) methylenetetrahydrofolate reductase variants by multiplex PCR using fluorescence scanning technology.
Saffroy R; Lemoine A; Haas P; Tindiliere F; Marion S; Debuire B
Genet Test; 2002; 6(3):233-6. PubMed ID: 12490067
[TBL] [Abstract][Full Text] [Related]
10. [C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism].
Avdonin PV; Kirienko AI; Kozhevnikova LM; Shostak NA; Babadaeva NM; Leont'ev SG; Petukhov EB; Kubatiev AA; Savel'ev VS
Ter Arkh; 2006; 78(6):70-6. PubMed ID: 16881367
[TBL] [Abstract][Full Text] [Related]
11. [Genetics of blood coagulation in young stroke patients].
Pongrácz E; Tordai A; Csornai M; Nagy Z
Ideggyogy Sz; 2002 Mar; 55(3-4):111-7. PubMed ID: 12122980
[TBL] [Abstract][Full Text] [Related]
12. Factor V Leiden and thermolabile methylenetetrahydrofolate reductase in extreme old age.
Rees DC; Liu YT; Cox MJ; Elliott P; Wainscoat JS
Thromb Haemost; 1997 Nov; 78(5):1357-9. PubMed ID: 9408019
[TBL] [Abstract][Full Text] [Related]
13. Maternal and fetal inherited thrombophilias are not related to the development of severe preeclampsia.
Livingston JC; Barton JR; Park V; Haddad B; Phillips O; Sibai BM
Am J Obstet Gynecol; 2001 Jul; 185(1):153-7. PubMed ID: 11483920
[TBL] [Abstract][Full Text] [Related]
14. Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes.
Alhenc-Gelas M; Arnaud E; Nicaud V; Aubry ML; Fiessinger JN; Aiach M; Emmerich J
Thromb Haemost; 1999 Apr; 81(4):506-10. PubMed ID: 10235429
[TBL] [Abstract][Full Text] [Related]
15. Rapid detection of prothrombotic mutations of prothrombin (G20210A), factor V (G1691A), and methylenetetrahydrofolate reductase (C677T) by real-time fluorescence PCR with the LightCycler.
von Ahsen N; Schütz E; Armstrong VW; Oellerich M
Clin Chem; 1999 May; 45(5):694-6. PubMed ID: 10222362
[No Abstract] [Full Text] [Related]
16. 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]
17. [Prevalence of factor V Leiden, hyperhomocysteinemia, prothrombin G20210A, and methylene tetrahydrofolate reductase C677T mutations in obstetrical complications].
Verdy E; Berkane N; Magdelaine A; Soubrier F; Uzan S
Ann Biol Clin (Paris); 1999; 57(5):539-44. PubMed ID: 10518055
[TBL] [Abstract][Full Text] [Related]
18. Prevalence of factor V Leiden and methylenetetrahydrofolate reductase C677T mutations in Azerbaijan.
Gurgey A; Rustemov R; Parlak H; Balta G
Thromb Haemost; 1998 Sep; 80(3):520-1. PubMed ID: 9759638
[No Abstract] [Full Text] [Related]
19. The 4G/4G polymorphism of the hypofibrinolytic plasminogen activator inhibitor type 1 gene: an independent risk factor for serious pregnancy complications.
Glueck CJ; Phillips H; Cameron D; Wang P; Fontaine RN; Moore SK; Sieve-Smith L; Tracy T
Metabolism; 2000 Jul; 49(7):845-52. PubMed ID: 10909993
[TBL] [Abstract][Full Text] [Related]
20. Application of the TaqMan-PCR for genotyping of the prothrombin G20210A mutation and of the thermolabile methylenetetrahydrofolate reductase mutation.
Happich D; Madlener K; Schwaab R; Hanfland P; Pötzsch B
Thromb Haemost; 2000 Jul; 84(1):144-5. PubMed ID: 10928490
[No Abstract] [Full Text] [Related]
[Next] [New Search]
