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 TitleAuthors / EditorsDate
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Clinical Consequences and Molecular Bases of Low Fibrinogen Levels Neerman Arbez, Marguerite; Casini, Alessandro 2018
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KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis Gueneau, Lucie; Fish, Richard; Shamseldin, Hanan E.; Voisin, Norine; ... Reymond, Alexandre 2018
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Inactivation of AMMECR1 is associated with growth, bone, and heart alterations Moysés-Oliveira, Mariana; Giannuzzi, Giuliana; Fish, Richard; Rosenfeld, Jill A; ... Reymond, Alexandre 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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A fibrin biofilm covers blood clots and protects from microbial invasion Macrae, Fraser L; Duval, Cédric; Papareddy, Praveen; Baker, Stephen R; ... Ariëns, Robert As 2018
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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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Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis Tajdar, Mercedeh; Orlando, Christelle; Casini, Alessandro; Herpol, Margaux; ... Jochmans, Kristin 2017
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A novel fibrinogen mutation: FGA g. 3057 C > T (p. Arg104 > Cys) impairs fibrinogen secretion Marchi, R; Linares, M; Rojas, H; Ruiz-Sáez, A; ... Brennan, S O 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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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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Diagnostic des anomalies congénitales du fibrinogène Lebreton, Aurélien; Casini, Alessandro 2016
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A comprehensive high-throughput sequencing test for the diagnosis of inherited bleeding, thrombotic and platelet disorders Simeoni, Ilenia 2016
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Can the phenotype of inherited fibrinogen disorders be predicted? Casini, Alessandro; De Moerloose, Philippe 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 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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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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