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 TitleAuthors / EditorsDate
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Molecular characterization of two hypofibrinogenemic patients associated with a novel FGG IVS6+23T>A substitution and a previously reported FGB IVS6-10_16delTTTG deletion Amri, Yessine; Dabboubi, Rym; Mghaieth, Fathia; Zili, Mohamed; ... Toumi, Nour El Houda 2020
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Management of bleeding and invasive procedures in haemophilia A patients with inhibitor treated with emicizumab (Hemlibra®): Proposals from the French network on inherited bleeding disorders (MHEMO), the French Reference Centre on Haemophilia, in collaboration with the French Working Group on Perioperative Haemostasis (GIHP) Susen, Sophie; Gruel, Yves; Godier, Anne; Harroche, Annie; ... Négrier, Claude 2019
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Fibrinogen concentrates in hereditary fibrinogen disorders: past, present and future Casini, Alessandro; De Moerloose, Philippe 2019
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The impact of haemophilia on the social status and the health-related quality of life in adult Lebanese persons with haemophilia Naous, Elie; De Moerloose, Philippe; Sleilaty, Ghassan; Casini, Alessandro; Djambas Khayat, Claudia 2019
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Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: a systematic literature review Valiton, Vivian; Hugon-Rodin, Justine; Fontana, Pierre; Neerman Arbez, Marguerite; Casini, Alessandro 2019
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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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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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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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Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia Casini, Alessandro; Vilar, Rui; Beauverd, Yan; Aslan, D; ... Neerman Arbez, Marguerite 2017
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Management of congenital quantitative fibrinogen disorders: a Delphi consensus 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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Can the phenotype of inherited fibrinogen disorders be predicted? Casini, Alessandro; De Moerloose, Philippe 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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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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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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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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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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