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Journal Abstract Search
108 related items for PubMed ID: 21885950
1. Painful congestion of the lower limbs and recurrent fever. Staubach S, Hug M, Mudra H. Blood Coagul Fibrinolysis; 2011 Dec; 22(8):752-5. PubMed ID: 21885950 [Abstract] [Full Text] [Related]
2. The influence of factor V Leiden and G20210A prothrombin mutation on the presence of residual vein obstruction after idiopathic deep-vein thrombosis of the lower limbs. Cosmi B, Legnani C, Pengo V, Ghirarduzzi A, Testa S, Poli D, Prisco D, Tripodi A, Palareti G, PROLONG Investigators (on behalf of FCSA, Italian Federation of Anticoagulation Clinics). Thromb Haemost; 2013 Mar; 109(3):510-6. PubMed ID: 23306310 [Abstract] [Full Text] [Related]
3. [Agenesis of inferior vena cava combined with multiple genetic predisposition in the case of deep venous thrombosis in a young male]. Vidra T, Szomor A, Battyáni I, Mühl D, Losonczy H. Orv Hetil; 2003 Nov 16; 144(46):2283-6. PubMed ID: 14702924 [Abstract] [Full Text] [Related]
4. Deep venous thrombosis caused by inferior vena cava atresia and hereditary thrombophilia. Rose SS, Ali Y, Kumar A, Bekos TJ, Saidi P. Am J Med Sci; 2009 Jan 16; 337(1):67-70. PubMed ID: 19002010 [Abstract] [Full Text] [Related]
5. Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives. Aznar J, Vayá A, Estellés A, Mira Y, Seguí R, Villa P, Ferrando F, Falcó C, Corella D, España F. Haematologica; 2000 Dec 16; 85(12):1271-6. PubMed ID: 11114134 [Abstract] [Full Text] [Related]
6. The PORtromb Project: prothrombin G20210A mutation and venous thromboembolism in young people. Mansilha A, Araújo F, Sampaio S, Cunha Ribeiro LM, Braga A. Cardiovasc Surg; 2002 Feb 16; 10(1):45-8. PubMed ID: 11790575 [Abstract] [Full Text] [Related]
7. Upper-extremity deep vein thrombosis in a patient on clozapine therapy carrying the prothrombin G20210A mutation. Vayá A, Lopez M, Plumé G, Ribes J. Pathophysiol Haemost Thromb; 2008 Feb 16; 36(2):105-7. PubMed ID: 19127092 [Abstract] [Full Text] [Related]
8. An uncommon clinical condition: chronic thrombosis of the inferior vena cava. A case report and review of literature. Donati F, Misuraca L, Grigoratos C, Violo C, Vannucci S, Balbarini A. Monaldi Arch Chest Dis; 2010 Mar 16; 74(1):36-9. PubMed ID: 20925177 [Abstract] [Full Text] [Related]
9. Risk factors and recurrence rate of primary deep vein thrombosis of the upper extremities. Martinelli I, Battaglioli T, Bucciarelli P, Passamonti SM, Mannucci PM. Circulation; 2004 Aug 03; 110(5):566-70. PubMed ID: 15262837 [Abstract] [Full Text] [Related]
10. 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 09; 341(11):801-6. PubMed ID: 10477778 [Abstract] [Full Text] [Related]
11. [Hereditary thrombophilia and systemic sclerosis. An unusual case report]. Minenna G, Albanese L, D'Amore S, Scagliusi P, D'Amore M. Recenti Prog Med; 2007 Mar 09; 98(3):175-8. PubMed ID: 17484164 [Abstract] [Full Text] [Related]
12. Thrombosis in systemic lupus erythematosus: effect of inherited thrombophilic mutations. Pamuk GE, Turgut B, Vural O, Demir M, Soy M, Bozkurt G, Celik H. Clin Rheumatol; 2003 Oct 09; 22(4-5):336-8. PubMed ID: 14576995 [Abstract] [Full Text] [Related]
13. Impact of coagulation in the development of thromboembolic events in patients with spinal cord injury. de Campos Guerra JC, Mourão MA, França CN, da Rosa CD, Burattini MN. Spinal Cord; 2014 Apr 09; 52(4):327-32. PubMed ID: 24513719 [Abstract] [Full Text] [Related]
14. Portal, splenic and mesenteric vein thrombosis in a patient double heterozygous for factor V Leiden and prothrombin G20210A mutation. Grouzi E, Politou M, Douramani P, Merkouri E, Gialeraki A, Brountzos H, Perros G, Travlou A. Blood Coagul Fibrinolysis; 2009 Dec 09; 20(8):722-5. PubMed ID: 19734780 [Abstract] [Full Text] [Related]
15. [Purpura fulminans, venous thrombosis and constitutional thrombophilia in an infant]. Fadil F, Elfatoiki F, Mortaji K, Lasry F, Itri M, Khadir K, Benchikhi H, Sarbati N, Nadifi S. Arch Pediatr; 2013 May 09; 20(5):499-502. PubMed ID: 23566584 [Abstract] [Full Text] [Related]
16. Inherited and acquired thrombophilic alterations in patients with superficial vein thrombosis of lower limbs. Legnani C, Cini M, Cosmi B, Filippini M, Favaretto E, Palareti G. Thromb Haemost; 2014 Jun 09; 111(6):1194-6. PubMed ID: 24500135 [No Abstract] [Full Text] [Related]
17. The contribution of factor V Leiden and prothrombin G20210A mutation to the risk of central venous catheter-related thrombosis. Van Rooden CJ, Rosendaal FR, Meinders AE, Van Oostayen JA, Van Der Meer FJ, Huisman MV. Haematologica; 2004 Feb 09; 89(2):201-6. PubMed ID: 15003896 [Abstract] [Full Text] [Related]
18. Coexistence of hypofibrinogenemia and factor V Leiden mutation: is the balance shifted to thrombosis? Miljić P, Nedeljkov-Jančić R, Zuvela M, Subota V, Dorđević V. Blood Coagul Fibrinolysis; 2014 Sep 09; 25(6):628-30. PubMed ID: 24637696 [Abstract] [Full Text] [Related]
19. Duration of Anticoagulation Therapy in Patients with Genetic Inherited Thrombophilia. Bojovski I, Stankovic S, Petlichkovski A, Bosevski M. Pril (Makedon Akad Nauk Umet Odd Med Nauki); 2022 Jul 13; 43(2):33-40. PubMed ID: 35843922 [Abstract] [Full Text] [Related]
20. Protein S deficiency with a PROS1 gene mutation in a patient presenting with mesenteric venous thrombosis following total colectomy. Ji M, Yoon SN, Lee W, Jang S, Park SH, Kim DY, Chun S, Min WK. Blood Coagul Fibrinolysis; 2011 Oct 13; 22(7):619-21. PubMed ID: 21799399 [Abstract] [Full Text] [Related] Page: [Next] [New Search]