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 TitleAuthors / EditorsDate
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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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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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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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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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Clinical Features and Management of Congenital Fibrinogen Deficiencies Casini, Alessandro; De Moerloose, Philippe; Neerman-Arbez, Marguerite 2016
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A comprehensive high-throughput sequencing test for the diagnosis of inherited bleeding, thrombotic and platelet disorders Simeoni, Ilenia; Stephens, Jonathan C; Hu, Fengyuan; Deevi, Sri V V; ... Turro, Ernest 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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Diagnostic des anomalies congénitales du fibrinogène Lebreton, Aurélien; Casini, Alessandro 2016
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Thromboembolism in patients with congenital afibrinogenaemia. Long-term observational data and systematic review Nagler, Michael; Kremer Hovinga, Johanna A; Alberio, Lorenzo; Peter-Salonen, Kristiina; ... Lämmle, Bernhard 2016
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GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability Lodder, Elisabeth M; De Nittis, Pasquelena; Koopman, Charlotte D; Wiszniewski, Wojciech; ... Merla, Giuseppe 2016
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Natural history of patients with congenital dysfibrinogenemia Casini, Alessandro; Blondon, Marc; Lebreton, Aurelien; Koegel, Jeremie; ... De Moerloose, Philippe 2015
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αIIbβ3 variants defined by next-generation sequencing: predicting variants likely to cause Glanzmann thrombasthenia Buitrago, Lorena; Rendon, Augusto; Liang, Yupu; Simeoni, Ilenia; ... Coller, Barry S 2015
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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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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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Fibrin clot structure in patients with congenital dysfibrinogenaemia Casini, Alessandro; Duval, C; Pan, X; Tintillier, V; ... Ariëns, R A S 2015
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Integrated analysis of mRNA and miRNA expression in response to interleukin-6 in hepatocytes Lukowski, Samuel; Fish, Richard; Martin-Levilain, Juliette; Gonelle-Gispert, Carmen; ... Neerman-Arbez, Marguerite 2015
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