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Haemophilia : the Official Journal of the World Federation of Hemophilia|December 18, 2007
Increased frequency of the CTLA-4 49 A/G polymorphism in patients with acquired haemophilia A compared to healthy controlsA Pavlova, A Diaz-Lacava, H Zeitler, et al.Proceedings of the National Academy of Sciences of the United States of America|October 11, 1991
Molecular characterization of mild-to-moderate hemophilia A: detection of the mutation in 25 of 29 patients by denaturing gradient gel electrophoresisM Higuchi, S E Antonarakis, L Kasch, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|March 25, 2010
Mutations affecting disulphide bonds contribute to a fairly common prevalence of F13B gene defects: results of a genetic study in 14 families with factor XIII B deficiencyV Ivaskevicius, A Biswas, R Loreth, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|January 11, 2007
Osteoporosis in haemophilia - an underestimated comorbidity?T A Wallny, D T Scholz, J Oldenburg, et al.Journal of Thrombosis and Haemostasis : JTH|March 5, 2013
A new cell culture-based assay quantifies vitamin K 2,3-epoxide reductase complex subunit 1 function and reveals warfarin resistance phenotypes not shown by the dithiothreitol-driven VKOR assayA Fregin, K J Czogalla, J Gansler, et al.British Journal of Haematology|April 12, 2001
Lithuanian haemophilia A and B registry comprising phenotypic and genotypic dataV Ivaskevicius, R Jurgutis, S Rost, et al.Hamostaseologie|November 6, 2015
Neoplasm-induced bleeding in inherited, heterozygous FXIII-A deficiencyV Ivaškevičius, G Goldmann, A Biswas, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|March 25, 2010
Correlation of transient elastography with APRI and FIB-4 in a cohort of patients with congenital bleeding disorders and HCV or HIV/HCV coinfectionN Vidovic, R S Lochowsky, G Goldmann, et al.Haemophilia : the Official Journal of the World Federation of Hemophilia|November 22, 2007
Molecular characterization of five Italian families with inherited severe factor XIII deficiencyG Castaman, S H Giacomelli, V Ivaskevicius, et al.Journal of Thrombosis and Haemostasis : JTH|January 13, 2012
Monitoring of plasma levels of activated protein C using a clinically applicable oligonucleotide-based enzyme capture assayJ Müller, M Friedrich, T Becher, et al.Pageof 33