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Haemophilia : the Official Journal of the World Federation of Hemophilia|April 27, 2011
A retrospective study to describe the incidence of moderate to severe allergic reactions to factor IX in subjects with haemophilia BM Recht, H Pollmann, A Tagliaferri, et al.
Hamostaseologie|September 11, 2012
[Haemophilia treatment centres in Germany]R Zimmermann, B Eifrig, H Lenk, et al.
Human Mutation|December 19, 2001
Seven novel and four recurrent point mutations in the factor VIII (F8C) geneN Bogdanova, B Lemcke, A Markoff, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 20, 2009
Haemoassist--a hand-held electronic patient diary for haemophilia home careW Mondorf, B Siegmund, R Mahnel, et al.
Deutsche Medizinische Wochenschrift (1946)|October 28, 1983
[Vitamin K deficiency hemorrhages in 4 exclusively breast-fed infants 4 to 6 weeks of age]A H Sutor, H Pancochar, H Niederhoff, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 22, 2011
The relative burden of haemophilia A and the impact of target joint development on health-related quality of life: results from the ADVATE Post-Authorization Safety Surveillance (PASS) studyR Klamroth, H Pollmann, C Hermans, et al.
Hamostaseologie|February 5, 2003
Haemophilia and thrombophilia. What do we learn about combined inheritance of both genetic variations?U Nowak-Göttl, C Escuriola, K Kurnik, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 21, 2007
European study on orthopaedic status of haemophilia patients with inhibitorsM Morfini, S Haya, G Tagariello, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|August 22, 2006
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 geneF H Herrmann, G Auerswald, A Ruiz-Saez, et al.
Pediatrics|June 1, 1997
Lipoprotein (a): its role in childhood thromboembolismU Nowak-Göttl, O Debus, M Findeisen, et al.
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