Showing results (41-50 of 75) with videos related to

Sort By:
Pageof 8
Annals of Hematology|April 27, 2002
Hereditary spherocytosis and hemochromatosisJ B Brandenberg, F Demarmels Biasiutti, H U Lutz, et al.
European Journal of Clinical Investigation|March 12, 2002
Haemochromatosis mutations and ferritin in myocardial infarction: a case-control studyDirk Claeys, M Walting, F Julmy, et al.
Atherosclerosis|July 27, 2001
Increased fibrin monomer plasma concentration in stable coronary artery disease in patients without oral anticoagulationM Redondo, C Caliezi, F D Biasiutti, et al.
British Journal of Haematology|July 27, 2001
Protein Z in ischaemic strokeK Kobelt, F D Biasiutti, H P Mattle, et al.
Schweizerische Medizinische Wochenschrift|July 26, 2000
[Patient self-monitoring of oral anticoagulation with CoaguChek]C Caliezi, M Waber, D Pfiffner, et al.
Blood|August 15, 1994
Coagulation factor XII Locarno: the functional defect is caused by the amino acid substitution Arg 353-->Pro leading to loss of a kallikrein cleavage siteJ K Hovinga, J Schaller, H Stricker, et al.
Pharmacological Reviews|March 4, 2000
C1-Esterase inhibitor: an anti-inflammatory agent and its potential use in the treatment of diseases other than hereditary angioedemaC Caliezi, W A Wuillemin, S Zeerleder, et al.
European Journal of Immunogenetics : Official Journal of the British Society for Histocompatibility and Immunogenetics|June 6, 2003
Association of ABO histo-blood group B allele with myocardial infarctionU E Nydegger, W A Wuillemin, F Julmy, et al.
Thrombosis and Haemostasis|July 31, 1998
Is plasminogen deficiency a thrombotic risk factor? A study on 23 thrombophilic patients and their family membersF Demarmels Biasiutti, I Sulzer, B Stucki, et al.
Thrombosis and Haemostasis|November 2, 1999
Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency--a study on 73 subjects from 14 Swiss familiesS Zeerleder, M Schloesser, M Redondo, et al.
Pageof 8