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 TitleAuthors / EditorsDate
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Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization Amri, Y; Jouini, H; Becheur, M; Dabboubi, R; ... Toumi, N E H 2017
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Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia Casini, Alessandro; Vilarino, Raquel; Beauverd, Yan; Aslan, D; ... Neerman Arbez, Marguerite 2017
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Subthalamic nucleus deep brain stimulation for Parkinson's disease in a patient with severe haemophilia A. Boehlen, Françoise; Burkhard, Pierre; Momjian, Shahan Marc; Fontana, Pierre 2017
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Impact of a product-specific reference standard for the measurement of a PEGylated rFVIII activity: the Swiss Multicentre Field Study Bulla, O; Poncet, Antoine; Alberio, L; Asmis, L M; ... Fontana, Pierre 2017
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Management of congenital quantitative fibrinogen disorders: a Delphi consensus Casini, Alessandro; De Moerloose, Philippe 2016
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Can the phenotype of inherited fibrinogen disorders be predicted? Casini, Alessandro; De Moerloose, Philippe 2016
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How to compare cardiovascular disease and risk factors in elderly patients with haemophilia with the general population Berger, K; Schopohl, D; Lowe, G; Holme, P A; ... Klamroth, R 2016
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Hypertension, haematuria and renal functioning in haemophilia - a cross-sectional study in Europe Holme, P. A.; Combescure, Christophe; Tait, R.C.; Berntorp, E.; ... De Moerloose, Philippe 2016
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Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature Casini, Alessandro; Sokollik, C; Lukowski, Samuel; Lurz, E; ... Neerman Arbez, Marguerite 2015
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Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis Lebreton, A; Casini, Alessandro; Alhayek, R; Kouteich, K L; ... De Moerloose, Philippe 2015
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The role of prophylaxis in bleeding disorders Berntorp, E.; De Moerloose, Philippe; Ljung, R. C. 2010
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Replacement therapy for invasive procedures in patients with haemophilia: literature review, European survey and recommendations Hermans, C.; Altisent, C.; Batorova, A.; Chambost, H.; ... Dolan, G. 2009
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European curriculum for thrombosis and haemostasis Astermark, J.; Negrier, C.; Hermans, C.; Holme, P. A.; ... Ludlam, C. A. 2009
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A survey of adherence to haemophilia therapy in six European countries: results and recommendations De Moerloose, Philippe; Urbancik, W.; Van Den Berg, H M.; Richards, M. 2008
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Molecular analysis of F8 in Lebanese haemophilia A patients: novel mutations and phenotype-genotype correlation Djambas Khayat, C.; Salem, N.; Chouery, E.; Corbani, S.; ... Mégarbané, A. 2008
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Rare bleeding disorders Peyvandi, F.; Cattaneo, M.; Inbal, A.; De Moerloose, Philippe; Spreafico, M. 2008
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Induction of immune tolerance with recombinant factor VIII in haemophilia A patients with inhibitors Batlle, J; Lopez, M F; Brackmann, H H; Gaillard, S; ... Stieltjes, N 1999
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Molecular genetics of coagulation factor VIII gene and haemophilia A Antonarakis, Stylianos 1998