BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 16848214)

  • 1. [Recurrent incomplete central retinal vein occlusion in a patient with hereditary thrombophilia].
    Duić J; Gverić-Krecak V
    Acta Med Croatica; 2006; 60(2):171-4. PubMed ID: 16848214
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ocular vascular thrombotic events: central retinal vein and central retinal artery occlusions.
    Glueck CJ; Ping Wang ; Hutchins R; Petersen MR; Golnik K
    Clin Appl Thromb Hemost; 2008 Jul; 14(3):286-94. PubMed ID: 18160589
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrent central retinal vein occlusion in a young thrombophilic patient with factor V Leiden mutation.
    Incorvaia C; Bandello F; Parmeggiani F; D'Angelo S; Costagliola C; Sebastiani A
    Eur J Ophthalmol; 2002; 12(2):131-4. PubMed ID: 12022286
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [Thrombophilia as a risk factor for central retinal vein occlusion].
    Undas A; Kubicka-Trzaska A
    Klin Oczna; 2003; 105(3-4):221-4. PubMed ID: 14552191
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial thrombophilia and retinal vein occlusion.
    Backhouse O; Parapia L; Mahomed I; Lee D
    Eye (Lond); 2000 Feb; 14 ( Pt 1)():13-7. PubMed ID: 10755093
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.
    Coulam CB; Jeyendran RS; Fishel LA; Roussev R
    Am J Reprod Immunol; 2006 May; 55(5):360-8. PubMed ID: 16635210
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CENTRAL RETINAL VEIN OCCLUSION IN OTHERWISE HEALTHY CHILDREN AND ADOLESCENTS: Association With Multigenetic Variants of Thrombophilia.
    Bremond-Gignac D; Daruich A; Gallet M; Menoud PA; Nowomiejska K; Rejdak R; Behar-Cohen F; Benkhalifa M; Copin H
    Retina; 2020 Jul; 40(7):1339-1343. PubMed ID: 31095065
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prothrombin polymorphism A19911G, factor V HR2 haplotype A4070G, and plasminogen activator-inhibitor-1 polymorphism 4G/5G and the risk of retinal vein occlusion.
    Kuhli-Hattenbach C; Hellstern P; Nägler DK; Kohnen T; Hattenbach LO
    Ophthalmic Genet; 2017; 38(5):413-417. PubMed ID: 28085526
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.
    Kabukcu S; Keskin N; Keskin A; Atalay E
    Clin Appl Thromb Hemost; 2007 Apr; 13(2):166-71. PubMed ID: 17456626
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].
    Kovacheva K; Ivanov P; Konova E; Simeonova M; Komsa-Penkova R
    Akush Ginekol (Sofiia); 2007; 46(7):10-6. PubMed ID: 18333414
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The factor V Leiden mutation, high factor VIII, and high plasminogen activator inhibitor activity: etiologies for sporadic miscarriage.
    Glueck CJ; Pranikoff J; Aregawi D; Haque M; Zhu B; Tracy T; Wang P
    Metabolism; 2005 Oct; 54(10):1345-9. PubMed ID: 16154434
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. MTHFR C 677T mutation and 4G/5G PAI-1 polymorphism in patient with polycystic ovarian syndrome.
    Radaković B; Goldstajn MS
    Coll Antropol; 2007 Sep; 31(3):919-21. PubMed ID: 18041407
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Thrombophilic mutations and risk of retinal vein occlusion.
    Biancardi AL; Gadelha T; Borges WI; Vieira de Moraes H; Spector N
    Arq Bras Oftalmol; 2007; 70(6):971-4. PubMed ID: 18235909
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Evaluation of coagulopathies and fibrinolytic abnormalities in central retinal vein occlusion in patients under 60 years of age].
    Tea S; Barrali M; Racadot E; Delbosc B
    J Fr Ophtalmol; 2013 Jan; 36(1):5-11. PubMed ID: 23238070
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Combined thrombophilic mutations in women with unexplained recurrent miscarriage.
    Sotiriadis A; Vartholomatos G; Pavlou M; Kolaitis N; Dova L; Stefos T; Paraskevaidis E; Kalantaridou SN
    Am J Reprod Immunol; 2007 Feb; 57(2):133-41. PubMed ID: 17217367
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.