kw.\*:("G1691A")
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Analysis of some clinical and laboratory aspects of adolescent patients with thrombosisGURGEY, Aytemiz; BALTA, Gunay; GUMRUK, Fatma et al.Blood coagulation & fibrinolysis. 2004, Vol 15, Num 8, pp 657-662, issn 0957-5235, 6 p.Article
Prevalence of the Factor V G1691A and the Factor II/prothrombin G20210A gene polymorphisms among TamiliansANGELINE, T; BENTLEY, Heather A; HAWK, Arnold B et al.Experimental and molecular pathology. 2005, Vol 79, Num 1, pp 9-13, issn 0014-4800, 5 p.Article
Clinical and laboratory evaluation of Turkish children with thrombosis for homozygous factor V G1691A mutationUNAL, Selma; BALTA, Gunay; DURU, Feride et al.Blood coagulation & fibrinolysis. 2004, Vol 15, Num 4, pp 343-346, issn 0957-5235, 4 p.Article
Outcome in children with purpura fulminans : Report on 16 patientsGÜRGEY, Aytemiz; AYTAC, Selin; KANRA, Guler et al.American journal of hematology. 2005, Vol 80, Num 1, pp 20-25, issn 0361-8609, 6 p.Article
Combined thrombophilic polymorphisms in women with idiopathic recurrent miscarriageHOHLAGSCHWANDTNER, Maria; UNFRIED, Gertrud; HEINZE, Georg et al.Fertility and sterility. 2003, Vol 79, Num 5, pp 1141-1148, issn 0015-0282, 8 p.Article
Thrombophilic gene mutations in cirrhotic patients with portal vein thrombosisERKAN, Ozlem; BOZDAYI, Abdurrahman M; UZUNALIMOGLU, Ozden et al.European journal of gastroenterology & hepatology. 2005, Vol 17, Num 3, pp 339-343, issn 0954-691X, 5 p.Article
Secondary prophylaxis with warfarin for recurrent thrombosis in a patient with Glanzmann thrombasthenia and F5 G1691AREZENDE, Suely Meireles.British journal of haematology. 2012, Vol 156, Num 1, pp 144-145, issn 0007-1048, 2 p.Article
Site of venous thromboembolism and prothrombotic mutations according to body mass index. Results from the EDITH studyDELLUC, Aurélien; LE MOIGNE, Emmanuelle; TROMEUR, Cécile et al.British journal of haematology. 2011, Vol 154, Num 4, pp 486-491, issn 0007-1048, 6 p.Article
Genetic susceptibility, smoking, obesity and risk of venous thromboembolismSEVERINSEN, Marianne T; OVERVAD, Kim; JOHNSEN, Søren P et al.British journal of haematology. 2010, Vol 149, Num 2, pp 273-279, issn 0007-1048, 7 p.Article
CBS 844ins68, MTHFR TT677 and EPCR 4031 ins23 genotypes in patients with deep-vein thrombosisGROSSMANN, Ralf; SCHWENDER, Stefan; GEISEN, Ulrich et al.Thrombosis research. 2002, Vol 107, Num 1-2, pp 13-15, issn 0049-3848, 3 p.Article