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Comparison of different activators of coagulation by turbidity analysis of hereditary dysfibrinogenemia and controls Marchi Cappelletti, Rita; Neerman Arbez, Marguerite; Gay, Valérie; Mourey, Guillaume; ... Casini, Alessandro 2021
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How I treat dysfibrinogenemia Casini, Alessandro; De Moerloose, Philippe 2021
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Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia Casini, Alessandro; von Mackensen, Sylvia; Santoro, Cristina; Djambas Khayat, Claudia; ... De Moerloose, Philippe 2021
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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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Heterogeneity of congenital afibrinogenemia, from epidemiology to clinical consequences and management Casini, Alessandro; Neerman Arbez, Marguerite; De Moerloose, Philippe 2020
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Fibrinogen concentrates in hereditary fibrinogen disorders: past, present and future Casini, Alessandro; De Moerloose, Philippe 2019
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Impaired factor XIII activation in patients with congenital afibrinogenemia Bridey, Françoise; Négrier, Claude; Duval, Cedric; Ariëns, Robert; ... Casini, Alessandro 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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Prevalence, persistence and clinical correlations of classic and novel antiphospholipid antibodies in systemic lupus erythematosus Marchetti, Tess; Ribi, Camillo; Perneger, Thomas; Trendelenburg, Marten; ... Chizzolini, Carlo 2018
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Mutational epidemiology of congenital fibrinogen disorders Casini, Alessandro; Blondon, Marc; Tintillier, Veronique; Goodyer, Matthew; ... Neerman Arbez, Marguerite 2018
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Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH Casini, Alessandro; Undas, A; Palla, R; Thachil, J; De Moerloose, Philippe 2018
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Patient-derived anti-β2GP1 antibodies recognize a peptide motif pattern and not a specific sequence of residues De Moerloose, Philippe; Fickentscher, Céline; Boehlen, Françoise; Tiercy, Jean-Marie; ... Brandt, Karim J 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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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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A multicenter study to assess the reproducibility of antiphospholipid antibody results produced by an automated system Devreese, K M; Poncet, Antoine; Lindhoff-Last, E; Musial, J; ... Fontana, Pierre 2017
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Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation Casini, Alessandro; Brungs, T; Lavenu-Bombled, C; Vilar, R; ... De Moerloose, Philippe 2017
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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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Congenital Disorders of Fibrinogen: Clinical Presentations, Diagnosis and Management Casini, Alessandro; De Moerloose, Philippe 2016
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Pregnancy Marchetti, T; De Moerloose, Philippe; Casini, Alessandro 2016
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Can the phenotype of inherited fibrinogen disorders be predicted? Casini, Alessandro; De Moerloose, Philippe 2016
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