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Laboratory Investigation of Thrombophilia / LABORATORIJSKO ISPITIVANJE TROMBOFILIJA

-72. 138. Andrew M, Vegh P, Johnston M, Bowker J, Ofosu F, Mitchell L. Maturation of the hemostatic system during childhood. Blood 1992; 80: 1998-2005. 139. Monagle P, Barnes C, Ignjatovic V, Furmedge J, Newall F, Chan A, et al. 139. Developmental haemostasis. Impact for clinical haemostasis laboratories. Thromb Haemost 2006; 95: 362-72. 140. Majkić-Singh N, Šumarac Z. Quality Indicators of the Pre-Analytical Phase. J Med Biochem 2012; 31: 174-83. 141. Favaloro EJ, McDonald D, Lippi G. Laboratory investigation of

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Introduction to Molecular Genetic Diagnostics / UVOD U MOLEKULARNU GENETIČU DIJAGNOSTIKU

-74. 17. Favaloro EJ, McDonald D, Lippi G. Laboratory investigation of thrombophilia: the good, the bad, and the ugly. Semin Thromb Hemost 2009; 35(7): 695-710. 18. Varga EA, Kujovich JL. Management of inherited thrombophilia: guide for genetics professionals. Clin Genet 2012; 81(1): 7-17. 19. Malarstig A, Buil A, Souto JC, Clarke R, Blanco-Vaca F, Fontcuberta J, et al. Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a fa mily-based genome-wide association study. Blood 2009; 114: 1417

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The Impact of the Gene Variants FV Leiden, FII G20210A, MTHFR C677T and PAI-1 4G/5G on Pregnancy Loss in Women from Central Serbia

in MTHFR with recurrent embryonic loss [Article in Bulgarian] Akush Ginekol (Sofiia). 2014;53(1):8-12. 33 Margetić S. Laboratory investigation of thrombophilia. J Med Biochem. 2014;33:28-46. 34 Ozdemir O, Yenicesu GI, Silan F, Koksal B, Atik S, Ozen F, Gol M, Cetin A. Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations. Genet Test Mol Biomarkers. 2012;16(4):279-286.

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