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 *

204 related articles for article (PubMed ID: 22168450)

  • 21. Determination of factor V Leiden mutation and R2 polymorphism in cis position.
    Oztürk A; Balli S; Akar N
    Clin Appl Thromb Hemost; 2013; 19(6):685-8. PubMed ID: 22589460
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Severe protein S deficiency associated with heterozygous factor V Leiden mutation in a child with purpura fulminans.
    Dogan Y; Aygun D; Yilmaz Y; Kanra G; Secmeer G; Besbas N; Gurgey A
    Pediatr Hematol Oncol; 2003; 20(1):1-5. PubMed ID: 12687747
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Risk of recurrent venous thrombosis in homozygous carriers and double heterozygous carriers of factor V Leiden and prothrombin G20210A.
    Lijfering WM; Middeldorp S; Veeger NJ; Hamulyák K; Prins MH; Büller HR; van der Meer J
    Circulation; 2010 Apr; 121(15):1706-12. PubMed ID: 20368522
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The 1691 G-->A mutation in the factor V gene: relationship to activated protein C (APC) resistance and thrombosis in 65 patients.
    Leroy-Matheron C; Levent M; Pignon JM; Mendonça C; Gouault-Heilmann M
    Thromb Haemost; 1996 Jan; 75(1):4-10. PubMed ID: 8713771
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Homozygous protein C deficiency with late onset venous thrombosis: identification and in vitro expression study of a novel Pro275Ser mutation.
    Yu T; Dai J; Liu H; Wang J; Ding Q; Wang H; Wang X; Fu Q
    Pathology; 2012 Jun; 44(4):348-53. PubMed ID: 22531345
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Factor V Leiden mutation is a risk factor for hepatic artery thrombosis in liver transplantation.
    Fan J; Nishida S; Selvaggi G; Levi D; Tekin A; Weppler D; Tzakis AG
    Transplant Proc; 2013 Jun; 45(5):1990-3. PubMed ID: 23769091
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Factor V Leiden and prothrombin G20210A mutations in Thai patients awaiting kidney transplant.
    Arnutti P; Nathalang O; Cowawintaweewat S; Prayoonwiwat W; Choovichian P
    Southeast Asian J Trop Med Public Health; 2002 Dec; 33(4):869-71. PubMed ID: 12757241
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Factor V Leiden: an additional risk factor for thrombosis in protein S deficient families?
    Koeleman BP; van Rumpt D; Hamulyák K; Reitsma PH; Bertina RM
    Thromb Haemost; 1995 Aug; 74(2):580-3. PubMed ID: 8584987
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].
    Miljić P; Rolović Z; Elezović I; Antunović P; Stanojević M; Colović M
    Srp Arh Celok Lek; 1999; 127(1-2):21-7. PubMed ID: 10377836
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Ischaemic stroke patients with heterozygous factor V Leiden present with multiple brain infarctions and widespread atherothrombotic disease.
    Haapaniemi E; Helenius J; Jakovljević D; Soinne L; Syrjälä M; Kaste M; Lassila R; Tatlisumak T
    Thromb Haemost; 2009 Jan; 101(1):145-50. PubMed ID: 19132201
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
    Zhou RF; Fu QH; Wang WB; Xie S; Hu YQ; Wang XF; Wang ZY; Wang HL
    Chin Med J (Engl); 2004 Jun; 117(6):813-7. PubMed ID: 15198878
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Paediatric presentation and outcome of congenital protein C deficiency in Japan.
    Ohga S; Kang D; Kinjo T; Ochiai M; Doi T; Ishimura M; Kayamori Y; Urata M; Yamamoto J; Suenobu SI; Kanegane H; Ikenoue T; Shirahata A; Hara T
    Haemophilia; 2013 May; 19(3):378-84. PubMed ID: 23379934
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Prevalence of factor V G1691A (Leiden) and prothrombin G20210A polymorphisms among apparently healthy Jordanians.
    Nusier MK; Radaideh AM; Ababneh NA; Qaqish BM; Alzoubi R; Khader Y; Mersa JY; Irshaid NM; El-Khateeb M
    Neuro Endocrinol Lett; 2007 Oct; 28(5):699-703. PubMed ID: 17984931
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Analysis of an hereditary protein C deficiency pedigree with compound heterozygous gene mutations].
    Yang LH; Zhu LQ; Yang XO; Wang MS; Li J; Chen BC; Jin YH; Zhang Z; Zheng FX
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):515-8. PubMed ID: 23042384
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation.
    De Stefano V; Martinelli I; Mannucci PM; Paciaroni K; Chiusolo P; Casorelli I; Rossi E; Leone G
    N Engl J Med; 1999 Sep; 341(11):801-6. PubMed ID: 10477778
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Protein C and protein S deficiency - practical diagnostic issues.
    Wypasek E; Undas A
    Adv Clin Exp Med; 2013; 22(4):459-67. PubMed ID: 23986205
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Family history is a poor screen for prothrombotic genes in children with stroke.
    Johal SC; Garg BP; Heiny ME; Williams LS; Saha C; Walsh LE; Golomb MR
    J Pediatr; 2006 Jan; 148(1):68-71. PubMed ID: 16423600
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Venous thrombotic risk in family members of unselected individuals with factor V Leiden.
    Lensen RP; Bertina RM; de Ronde H; Vandenbroucke JP; Rosendaal FR
    Thromb Haemost; 2000 Jun; 83(6):817-21. PubMed ID: 10896231
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The risk of symptomatic pulmonary embolism due to proximal deep venous thrombosis differs in patients with different types of inherited thrombophilia.
    Rossi E; Za T; Ciminello A; Leone G; De Stefano V
    Thromb Haemost; 2008 Jun; 99(6):1030-4. PubMed ID: 18521504
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Homozygosity for factor V Leiden leads to enhanced thrombosis and atherosclerosis in mice.
    Eitzman DT; Westrick RJ; Shen Y; Bodary PF; Gu S; Manning SL; Dobies SL; Ginsburg D
    Circulation; 2005 Apr; 111(14):1822-5. PubMed ID: 15809370
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.