167 related articles for article (PubMed ID: 11108898)
1. Prevalence of three prothrombotic polymorphisms. Factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C 677T in Argentina. On behalf of the Grupo Cooperativo Argentino de Hemostasia y Trombosis.
Genoud V; Castañon M; Annichino-Bizzacchi J; Korin J; Kordich L
Thromb Res; 2000 Nov; 100(3):127-31. PubMed ID: 11108898
[No Abstract] [Full Text] [Related]
2. Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos.
Ruiz-Argüelles GJ; Garcés-Eisele J; Reyes-Núñez V; Ramírez-Cisneros FJ
Am J Hematol; 2001 Jan; 66(1):28-31. PubMed ID: 11426488
[TBL] [Abstract][Full Text] [Related]
3. Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment.
Salomon O; Steinberg DM; Zivelin A; Gitel S; Dardik R; Rosenberg N; Berliner S; Inbal A; Many A; Lubetsky A; Varon D; Martinowitz U; Seligsohn U
Arterioscler Thromb Vasc Biol; 1999 Mar; 19(3):511-8. PubMed ID: 10073951
[TBL] [Abstract][Full Text] [Related]
4. Inherited thrombophilia genes in minorities.
Mack R; Chowdary D; Streck D; Dermody J
Genet Test; 1999; 3(4):371-3. PubMed ID: 10627946
[TBL] [Abstract][Full Text] [Related]
5. Prevalence of genetic mutations that predispose to thrombophilia in a Greek Cypriot population.
Angelopoulou K; Nicolaides A; Constantinou Deltas C
Clin Appl Thromb Hemost; 2000 Apr; 6(2):104-7. PubMed ID: 10775032
[TBL] [Abstract][Full Text] [Related]
6. Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults.
Voetsch B; Damasceno BP; Camargo EC; Massaro A; Bacheschi LA; Scaff M; Annichino-Bizzacchi JM; Arruda VR
Thromb Haemost; 2000 Feb; 83(2):229-33. PubMed ID: 10739378
[TBL] [Abstract][Full Text] [Related]
7. Outcome of kidney transplantation in patients with inherited thrombophilia: data of a prospective study.
Heidenreich S; Junker R; Wolters H; Lang D; Hessing S; Nitsche G; Nowak-Göttl U
J Am Soc Nephrol; 2003 Jan; 14(1):234-9. PubMed ID: 12506156
[TBL] [Abstract][Full Text] [Related]
8. Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors.
Nowak-Göttl U; Wermes C; Junker R; Koch HG; Schobess R; Fleischhack G; Schwabe D; Ehrenforth S
Blood; 1999 Mar; 93(5):1595-9. PubMed ID: 10029588
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Factor V Leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children.
Kenet G; Sadetzki S; Murad H; Martinowitz U; Rosenberg N; Gitel S; Rechavi G; Inbal A
Stroke; 2000 Jun; 31(6):1283-8. PubMed ID: 10835445
[TBL] [Abstract][Full Text] [Related]
11. The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels.
Cattaneo M; Chantarangkul V; Taioli E; Santos JH; Tagliabue L
Thromb Res; 1999 Jan; 93(1):1-8. PubMed ID: 10065893
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Prothrombotic genotypes are not associated with pre-eclampsia and gestational hypertension: results from a large population-based study and systematic review.
Morrison ER; Miedzybrodzka ZH; Campbell DM; Haites NE; Wilson BJ; Watson MS; Greaves M; Vickers MA
Thromb Haemost; 2002 May; 87(5):779-85. PubMed ID: 12038776
[TBL] [Abstract][Full Text] [Related]
15. Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population.
Lu Y; Zhao Y; Liu G; Wang X; Liu Z; Chen B; Hui R
Thromb Res; 2002 Apr; 106(1):7-12. PubMed ID: 12165282
[TBL] [Abstract][Full Text] [Related]
16. Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium.
Gerhardt A; Scharf RE; Beckmann MW; Struve S; Bender HG; Pillny M; Sandmann W; Zotz RB
N Engl J Med; 2000 Feb; 342(6):374-80. PubMed ID: 10666427
[TBL] [Abstract][Full Text] [Related]
17. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.
Almawi WY; Tamim H; Kreidy R; Timson G; Rahal E; Nabulsi M; Finan RR; Irani-Hakime N
J Thromb Thrombolysis; 2005 Jun; 19(3):189-96. PubMed ID: 16082606
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Lipoprotein (a) and genetic polymorphisms of clotting factor V, prothrombin, and methylenetetrahydrofolate reductase are risk factors of spontaneous ischemic stroke in childhood.
Nowak-Göttl U; Sträter R; Heinecke A; Junker R; Koch HG; Schuierer G; von Eckardstein A
Blood; 1999 Dec; 94(11):3678-82. PubMed ID: 10572079
[TBL] [Abstract][Full Text] [Related]
20. Thrombophilia: genetic polymorphisms and their association with retinal vascular occlusive disease.
Chak M; Wallace GR; Graham EM; Stanford MR
Br J Ophthalmol; 2001 Jul; 85(7):883-6. PubMed ID: 11423467
[No Abstract] [Full Text] [Related]
[Next] [New Search]