285 related articles for article (PubMed ID: 15449030)
1. Protein C system defects in Indian children with thrombosis.
Gupta PK; Ahmed RP; Bhattacharyya M; Kannan M; Biswas A; Kalra V; Saxena R
Ann Hematol; 2005 Feb; 84(2):85-8. PubMed ID: 15449030
[TBL] [Abstract][Full Text] [Related]
2. Evaluation of thrombotic children with malignancy.
Unal S; Varan A; Yalçin B; Büyükpamukçu M; Gürgey A
Ann Hematol; 2005 Jun; 84(6):395-9. PubMed ID: 15735962
[TBL] [Abstract][Full Text] [Related]
3. Congenital prothrombotic disorders in children with peripheral venous and arterial thromboses.
Albisetti M; Moeller A; Waldvogel K; Bernet-Buettiker V; Cannizzaro V; Anagnostopoulos A; Balmer C; Schmugge M
Acta Haematol; 2007; 117(3):149-55. PubMed ID: 17159337
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Hereditary deficiencies of antithrombin III, protein S, and the protein C pathway in Jordanian thrombosis patients.
Eid SS
Clin Lab Sci; 2002; 15(4):196-9. PubMed ID: 12776777
[TBL] [Abstract][Full Text] [Related]
6. Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis: a study from North India.
Bhattacharyya M; Makharia G; Kannan M; Ahmed RP; Gupta PK; Saxena R
Am J Clin Pathol; 2004 Jun; 121(6):844-7. PubMed ID: 15198356
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. The prevalence of factor V (G1691A), MTHFR (C677T) and PT (G20210A) gene mutations in arterial thrombosis.
Ozmen F; Ozmen MM; Ozalp N; Akar N
Ulus Travma Acil Cerrahi Derg; 2009 Mar; 15(2):113-9. PubMed ID: 19353312
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population.
Torres JD; Cardona H; Alvarez L; Cardona-Maya W; Castañeda SA; Quintero-Rivera F; Cadavid A; Bedoya G; Tobón L
Am J Hematol; 2006 Dec; 81(12):933-7. PubMed ID: 16917913
[TBL] [Abstract][Full Text] [Related]
12. The risk of recurrent venous thromboembolism in patients with inherited deficiency of natural anticoagulants antithrombin, protein C and protein S.
De Stefano V; Simioni P; Rossi E; Tormene D; Za T; Pagnan A; Leone G
Haematologica; 2006 May; 91(5):695-8. PubMed ID: 16670075
[TBL] [Abstract][Full Text] [Related]
13. Laboratory assessment of hypercoagulable state. A study in a group of patients with venous thromboembolism born in Chioggia.
Gessoni G; Valverde S; Canistro R; Trabuio E; Antico F; Manoni F
Minerva Med; 2007 Apr; 98(2):89-93. PubMed ID: 17519850
[TBL] [Abstract][Full Text] [Related]
14. Pro CR global: an effective screening test for thrombophilia.
Gupta PK; Ahmed R; Kannan M; Dwivedi SN; Choudhry VP; Saxena R
Am J Hematol; 2003 Nov; 74(3):208-10. PubMed ID: 14587054
[TBL] [Abstract][Full Text] [Related]
15. Nonstroke arterial thrombosis in children: Hacettepe experience.
Balci YI; Unal S; Gumruk F; Cetin M; Ozkutlu S; Gurgey A
Blood Coagul Fibrinolysis; 2008 Sep; 19(6):519-24. PubMed ID: 18685435
[TBL] [Abstract][Full Text] [Related]
16. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.
Yasa MH; Bolaman Z; Yukselen V; Kadikoylu G; Karaoglul AO; Batun S
Hepatogastroenterology; 2007; 54(77):1438-42. PubMed ID: 17708272
[TBL] [Abstract][Full Text] [Related]
17. Thrombophilias and recurrent pregnancy loss.
Kutteh WH; Triplett DA
Semin Reprod Med; 2006 Feb; 24(1):54-66. PubMed ID: 16418978
[TBL] [Abstract][Full Text] [Related]
18. Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study.
El-Karaksy H; El-Koofy N; El-Hawary M; Mostafa A; Aziz M; El-Shabrawi M; Mohsen NA; Kotb M; El-Raziky M; El-Sonoon MA; A-Kader H
Ann Hematol; 2004 Nov; 83(11):712-5. PubMed ID: 15309526
[TBL] [Abstract][Full Text] [Related]
19. Inherited thrombophilic factors do not increase central venous catheter blockage in children with malignancy.
Chung BH; Ma ES; Khong PL; Chan GC
Pediatr Blood Cancer; 2008 Oct; 51(4):509-12. PubMed ID: 18561172
[TBL] [Abstract][Full Text] [Related]
20. Significance of factor V, prothrombin, MTHFR, and PAI-1 genotypes in childhood cerebral thrombosis.
Ozyurek E; Balta G; Degerliyurt A; Parlak H; Aysun S; Gürgey A
Clin Appl Thromb Hemost; 2007 Apr; 13(2):154-60. PubMed ID: 17456624
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]