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Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutations Marchi Cappelletti, Rita; Ferreira Vilar Da Silva, Rui Filipe; Durual, Stéphane; Goodyer, Matthew; ... Casini, Alessandro 2021
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Hepatocellular type II fibrinogen inclusions in a patient with severe COVID-19 and hepatitis Fraga, Montserrat; Moradpour, Darius; Artru, Florent; Romailler, Elodie; ... Sempoux, Christine 2020
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Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A. Ferreira Vilar Da Silva, Rui Filipe; Casini, Alessandro; Fournel, Alexandra; Mourey, Guillaume; Neerman Arbez, Marguerite 2020
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A Unique Case of Acquired Hemophilia A Presenting with Transient Ischemic Attack Beauverd, Yan; Boehlen, Françoise; Fisch, Loraine; Sztajzel, Roman; ... Casini, Alessandro 2020
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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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Suggestions for thromboprophylaxis and laboratory monitoring for in-hospital patients with COVID-19 Casini, Alessandro; Alberio, Lorenzo; Angelillo-Scherrer, Anne; Fontana, Pierre; ... Asmis, Lars 2020
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Recommendations on the use of anticoagulants for the treatment of patients with heparin-induced thrombocytopenia in Switzerland Alberio, Lorenzo; Angelillo-Scherrer, Anne; Asmis, Lars; Casini, Alessandro; ... Wuillemin, Walter 2020
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From Routine to Research Laboratory: Strategies for the Diagnosis of Congenital Fibrinogen Disorders Casini, Alessandro 2020
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Safety of variceal band ligation in patients with cirrhosis and portal vein thrombosis treated with anticoagulant therapy: A retrospective study Ponthus, Simon; Spahr, Laurent François Joséph; Casini, Alessandro; Berney, Thierry; ... Elkrief, Laure 2020
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Fibrin(ogen) in human disease: both friend and foe Ferreira Vilar Da Silva, Rui Filipe; Fish, Richard; Casini, Alessandro; Neerman Arbez, Marguerite 2020
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Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype Simurda, Tomas; Casini, Alessandro; Stasko, Jan; Hudecek, Jan; ... Kubisz, Peter 2020
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A novel nonsense mutation in FBG (c.1421G>A;p.Trp474Ter) in the beta chain of fibrinogen causing hypofibrinogenemia with bleeding phenotype Simurda, Tomas; Ferreira Vilar Da Silva, Rui Filipe; Zolkova, Jana; Ceznerova, Eliska; ... Kubisz, Peter 2020
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Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: An EHA Consensus Report Rodeghiero, Francesco; Pabinger, Ingrid; Ragni, Margaret; Abdul-Kadir, Rezan; ... Key, Nigel 2019
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Congenital structural and functional fibrinogen disorders: a primer for internists Undas, Anetta; Casini, Alessandro 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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A unique factor XIII mutation in southeastern Iran with an unexpectedly high prevalence: khash factor XIII Dorgalaleh, Akbar; Tabibian, Shadi; Shams, Mahmood; Majid, Golbahar; ... Safa, Majid 2019
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Thrombin generation and fibrin clot structure after vitamin D supplementation Blondon, Marc; Biver, Emmanuel; Braillard, Olivia Thanh-Lan; Righini, Marc Philip; ... Casini, Alessandro 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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Hereditary fibrinogen disorders: toward a tailored management Casini, Alessandro 2019
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