Casini, Alessandro

 
 
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2021

Scientific Articles

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A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish familyGuipponi, Michel; Masclaux, Frédéric; Sloan Bena, Frédérique; Di Sanza, Corinne; ... Neerman Arbez, Marguerite
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Afibrinogenemia with two compound heterozygous mutations in FGA geneFeugray, Guillaume; Billoir, Paul; Casini, Alessandro; Neerman Arbez, Marguerite; ... Le Cam Duchez, Véronique
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Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemiaCasini, Alessandro; von Mackensen, Sylvia; Santoro, Cristina; Djambas Khayat, Claudia; ... De Moerloose, Philippe
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Comparison of different activators of coagulation by turbidity analysis of hereditary dysfibrinogenemia and controlsMarchi Cappelletti, Rita; Neerman Arbez, Marguerite; Gay, Valérie; Mourey, Guillaume; ... Casini, Alessandro
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Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutationsMarchi Cappelletti, Rita; Ferreira Vilar Da Silva, Rui Filipe; Durual, Stéphane; Goodyer, Matthew; ... Casini, Alessandro
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How I treat dysfibrinogenemiaCasini, Alessandro; De Moerloose, Philippe;
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Novel missense mutations affecting the structure of the conserved fibrinogen Bβ C-terminal domain cause congenital hypofibrinogenemiaBartolo, Raquel; Arbez, Maxime; Ferreira Vilar Da Silva, Rui Filipe; Szanto, Timea; ... Neerman Arbez, Marguerite
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Whole blood thromboelastometry by ROTEM and thrombin generation by genesia according to the genotype and clinical phenotype in congenital fibrinogen disordersSzanto, Timea; Lassila, Riitta; Lemponen, Marja; Lehtinen, Elina; ... Casini, Alessandro

2020

Scientific Articles

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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 phenotypeSimurda, Tomas; Ferreira Vilar Da Silva, Rui Filipe; Zolkova, Jana; Ceznerova, Eliska; ... Kubisz, Peter
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A Unique Case of Acquired Hemophilia A Presenting with Transient Ischemic AttackBeauverd, Yan; Boehlen, Françoise; Fisch, Loraine; Sztajzel, Roman; ... Casini, Alessandro
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Fibrin(ogen) in human disease: both friend and foeFerreira Vilar Da Silva, Rui Filipe; Fish, Richard; Casini, Alessandro; Neerman Arbez, Marguerite;
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From Routine to Research Laboratory: Strategies for the Diagnosis of Congenital Fibrinogen DisordersCasini, Alessandro;
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Hepatocellular type II fibrinogen inclusions in a patient with severe COVID-19 and hepatitisFraga, Montserrat; Moradpour, Darius; Artru, Florent; Romailler, Elodie; ... Sempoux, Christine
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Heterogeneity of congenital afibrinogenemia, from epidemiology to clinical consequences and managementCasini, Alessandro; Neerman Arbez, Marguerite; De Moerloose, Philippe;
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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
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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 deletionAmri, Yessine; Dabboubi, Rym; Mghaieth, Fathia; Zili, Mohamed; ... Toumi, Nour El Houda
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Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotypeSimurda, Tomas; Casini, Alessandro; Stasko, Jan; Hudecek, Jan; ... Kubisz, Peter
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Recommendations on the use of anticoagulants for the treatment of patients with heparin-induced thrombocytopenia in SwitzerlandAlberio, Lorenzo; Angelillo-Scherrer, Anne; Asmis, Lars; Casini, Alessandro; ... Wuillemin, Walter
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Safety of variceal band ligation in patients with cirrhosis and portal vein thrombosis treated with anticoagulant therapy: A retrospective studyPonthus, Simon; Spahr, Laurent François Joséph; Casini, Alessandro; Berney, Thierry; ... Elkrief, Laure
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Suggestions for thromboprophylaxis and laboratory monitoring for in-hospital patients with COVID-19Casini, Alessandro; Alberio, Lorenzo; Angelillo-Scherrer, Anne; Fontana, Pierre; ... Asmis, Lars
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Venous thromboembolism in COVID-19: systematic review of reported risks and current guidelinesFontana, Pierre; Casini, Alessandro; Robert-Ebadi, Helia; Glauser, Frédéric; ... Blondon, Marc

2019

Scientific Articles

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A unique factor XIII mutation in southeastern Iran with an unexpectedly high prevalence: khash factor XIIIDorgalaleh, Akbar; Tabibian, Shadi; Shams, Mahmood; Majid, Golbahar; ... Safa, Majid
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Congenital structural and functional fibrinogen disorders: a primer for internistsUndas, Anetta; Casini, Alessandro;
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Fibrinogen concentrates in hereditary fibrinogen disorders: past, present and futureCasini, Alessandro; De Moerloose, Philippe;
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Fundamentals for a Systematic Approach to Mild and Moderate Inherited Bleeding Disorders: An EHA Consensus ReportRodeghiero, Francesco; Pabinger, Ingrid; Ragni, Margaret; Abdul-Kadir, Rezan; ... Key, Nigel
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Impaired factor XIII activation in patients with congenital afibrinogenemiaBridey, Françoise; Négrier, Claude; Duval, Cedric; Ariëns, Robert; ... Casini, Alessandro
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Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: a systematic literature reviewValiton, Vivian; Hugon-Rodin, Justine; Fontana, Pierre; Neerman Arbez, Marguerite; Casini, Alessandro
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The impact of haemophilia on the social status and the health-related quality of life in adult Lebanese persons with haemophiliaNaous, Elie; De Moerloose, Philippe; Sleilaty, Ghassan; Casini, Alessandro; Djambas Khayat, Claudia
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Thrombin generation and fibrin clot structure after vitamin D supplementationBlondon, Marc; Biver, Emmanuel; Braillard, Olivia Thanh-Lan; Righini, Marc Philip; ... Casini, Alessandro

Privat-docent Thesis

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Hereditary fibrinogen disorders: toward a tailored managementCasini, Alessandro;
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