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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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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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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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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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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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Preoperative hemostatic assessment: a new and simple bleeding questionnaire Bonhomme, Fanny; Boehlen, Françoise; Clergue, François; De Moerloose, Philippe 2016
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Management of congenital quantitative fibrinogen disorders: a Delphi consensus Casini, Alessandro; 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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Clinical Features and Management of Congenital Fibrinogen Deficiencies Casini, Alessandro; De Moerloose, Philippe; Neerman Arbez, Marguerite 2016
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Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders Neerman Arbez, Marguerite; De Moerloose, Philippe; Casini, Alessandro 2016
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Factor concentrates for rare congenital coagulation disorders: where are we now? 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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F-actin dampens NLRP3 inflammasome activity via Flightless-I and LRRFIP2 Burger, Danielle; Fickentscher, Céline; De Moerloose, Philippe; Brandt, Karim 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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Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management Casini, Alessandro; Neerman Arbez, Marguerite; Ariëns, R A; 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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