337 related articles for article (PubMed ID: 11246543)
1. Interaction of heritable and estrogen-induced thrombophilia: possible etiologies for ischemic optic neuropathy and ischemic stroke.
Glueck CJ; Fontaine RN; Wang P
Thromb Haemost; 2001 Feb; 85(2):256-9. PubMed ID: 11246543
[TBL] [Abstract][Full Text] [Related]
2. Ocular vascular thrombotic events: a diagnostic window to familial thrombophilia (compound factor V Leiden and prothrombin gene heterozygosity) and thrombosis.
Glueck CJ; Wang P
Clin Appl Thromb Hemost; 2009 Feb; 15(1):12-8. PubMed ID: 18796459
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Nonarteritic anterior ischemic optic neuropathy: associations with homozygosity for the C677T methylenetetrahydrofolate reductase mutation.
Glueck CJ; Wang P; Bell H; Rangaraj V; Goldenberg N
J Lab Clin Med; 2004 Mar; 143(3):184-92. PubMed ID: 15007309
[TBL] [Abstract][Full Text] [Related]
5. [Risk of thrombophilia in carriers of thrombophilic genetic factors in unsuccessful assisted reproduction].
Ivanov P; Komsa-Penkova R; Kovacheva K; Konova E; Todorova K; Simeonova M; Ivanov I; Stoĭkov S; Popov I; Tanchev S; Bozhinova S
Akush Ginekol (Sofiia); 2007; 46(6):3-8. PubMed ID: 17974163
[TBL] [Abstract][Full Text] [Related]
6. The relationship of mutations in the MTHFR, prothrombin, and PAI-1 genes to plasma levels of homocysteine, prothrombin, and PAI-1 in children and adults.
Balasa VV; Gruppo RA; Glueck CJ; Stroop D; Becker A; Pillow A; Wang P
Thromb Haemost; 1999 May; 81(5):739-44. PubMed ID: 10365747
[TBL] [Abstract][Full Text] [Related]
7. Spectrum and prevalence of prothrombotic single nucleotide polymorphism profiles in the Greek Cypriot population.
Xenophontos SL; Hadjivassiliou M; Ayrton N; Karagrigoriou A; Pantzaris M; Nicolaides AN; Cariolou MA
Int Angiol; 2002 Dec; 21(4):322-9. PubMed ID: 12518110
[TBL] [Abstract][Full Text] [Related]
8. Ramifications of four concurrent thrombophilic mutations and one hypofibrinolytic mutation.
Glueck CJ; Goldenberg N; Wang P; Aregawi D
Clin Appl Thromb Hemost; 2004 Oct; 10(4):365-71. PubMed ID: 15497023
[TBL] [Abstract][Full Text] [Related]
9. Heritable thrombophilia and hypofibrinolysis. Possible causes of retinal vein occlusion.
Glueck CJ; Bell H; Vadlamani L; Gupta A; Fontaine RN; Wang P; Stroop D; Gruppo R
Arch Ophthalmol; 1999 Jan; 117(1):43-9. PubMed ID: 9930159
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. 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]
12. 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]
13. Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis.
Coulam CB; Wallis D; Weinstein J; DasGupta DS; Jeyendran RS
Am J Reprod Immunol; 2008 Nov; 60(5):426-31. PubMed ID: 18803625
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Large volume donor plasmapheresis in inherited thrombophilia implicated in arterial thrombosis.
Ovali E; Ratip S; Ozmenoglu M; Karti SS; Uçar F; Ukinç K; Yilmaz M; Koşucu P
Transfus Apher Sci; 2003 Jun; 28(3):201-6. PubMed ID: 12725943
[TBL] [Abstract][Full Text] [Related]
16. Risk Factors of Thrombophilia-Related Mutations for Early and Late Pregnancy Loss.
Borsi E; Potre O; Ionita I; Samfireag M; Secosan C; Potre C
Medicina (Kaunas); 2024 Mar; 60(4):. PubMed ID: 38674167
[No Abstract] [Full Text] [Related]
17. [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans].
Guo C; Guo Q; Gong Y; Chen B; Liu Q; Li J; Gao G; Zhou H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):295-7. PubMed ID: 12170465
[TBL] [Abstract][Full Text] [Related]
18. Amaurosis fugax: associations with heritable thrombophilia.
Glueck CJ; Goldenberg N; Bell H; Golnik K; Wang P
Clin Appl Thromb Hemost; 2005 Jul; 11(3):235-41. PubMed ID: 16015408
[TBL] [Abstract][Full Text] [Related]
19. Prediction of ischemic stroke in young Indians: is thrombophilia profiling a way out?
Chatterjee T; Gupta N; Choudhry VP; Behari M; Saxena R; Ashraf MZ
Blood Coagul Fibrinolysis; 2013 Jun; 24(4):449-53. PubMed ID: 23337710
[TBL] [Abstract][Full Text] [Related]
20. Homozygous G20210A transition in the prothrombin gene associated with severe venous thrombotic disease: two cases in a French family.
Zawadzki C; Gaveriaux V; Trillot N; Bauters A; Watel A; Alhenc-Gelas M; Preudhomme C; Jude B
Thromb Haemost; 1998 Dec; 80(6):1027-8. PubMed ID: 9869179
[No Abstract] [Full Text] [Related]
[Next] [New Search]