2020

Scientific Articles

unige:131188	Fibrin(ogen) in human disease: both friend and foe	Ferreira Vilar Da Silva, Rui Filipe; Fish, Richard; Casini, Alessandro; Neerman Arbez, Marguerite;
unige:135207	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
unige:131189	Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype	Simurda, Tomas; Casini, Alessandro; Stasko, Jan; Hudecek, Jan; ... Kubisz, Peter
unige:134292	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
unige:135208	Suggestions for thromboprophylaxis and laboratory monitoring for in-hospital patients with COVID-19	Casini, Alessandro; Alberio, Lorenzo; Angelillo-Scherrer, Anne; Fontana, Pierre; ... Asmis, Lars

2019

Scientific Articles

unige:124279	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
unige:127884	Congenital structural and functional fibrinogen disorders: a primer for internists	Undas, Anetta; Casini, Alessandro;
unige:127885	Fibrinogen concentrates in hereditary fibrinogen disorders: past, present and future	Casini, Alessandro; De Moerloose, Philippe;
unige:135206	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
unige:125939	Impaired factor XIII activation in patients with congenital afibrinogenemia	Bridey, Françoise; Négrier, Claude; Duval, Cedric; Ariëns, Robert; ... Casini, Alessandro
unige:122151	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
unige:128495	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
unige:127832	Thrombin generation and fibrin clot structure after vitamin D supplementation	Blondon, Marc; Biver, Emmanuel; Braillard, Olivia Thanh-Lan; Righini, Marc Philip; ... Casini, Alessandro

Privat-docent Thesis

unige:127607

Hereditary fibrinogen disorders: toward a tailored management

Casini, Alessandro;

2018

Scientific Articles

unige:107789	A fibrin biofilm covers blood clots and protects from microbial invasion	Macrae, Fraser L; Duval, Cédric; Papareddy, Praveen; Baker, Stephen R; ... Ariëns, Robert As
unige:111678	Acide tranexamique dans la prise en charge de l'hémorragie du postpartum : connaissances actuelles	Peter, Clarisse; Dereu, Domitille; Casini, Alessandro; Boulvain, Michel; Savoldelli, Georges Louis
unige:121244	Antithrombotiques dans le syndrome des anticorps antiphospholipides thrombotique	Chrysafi, Maria; Casini, Alessandro;
unige:101803	Clinical Consequences and Molecular Bases of Low Fibrinogen Levels	Neerman Arbez, Marguerite; Casini, Alessandro;
unige:107788	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
unige:115121	Mutational epidemiology of congenital fibrinogen disorders	Casini, Alessandro; Blondon, Marc; Tintillier, Veronique; Goodyer, Matthew; ... Neerman Arbez, Marguerite
unige:125822	Traitements antithrombotiques et anomalies constitutionnelles hémorragipares de l’hémostase	Casini, Alessandro; Fontana, Pierre; Lecompte, Thomas Pierre;

2017

Scientific Articles

unige:101804	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
unige:99479	Fibrinogen Mahdia: A congenitally abnormal fibrinogen characterized by defective fibrin polymerization	Amri, Y; Jouini, H; Becheur, M; Dabboubi, R; ... Toumi, N E H
unige:94324	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
unige:100661	Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis	Tajdar, Mercedeh; Orlando, Christelle; Casini, Alessandro; Herpol, Margaux; ... Jochmans, Kristin
unige:101840	Impact of pneumatic tube system transport for the monitoring of heparin therapy	Lebreton, Aurélien; Casini, Alessandro; Bulla, Oana; Fontana, Pierre;
unige:99478	Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia	Casini, Alessandro; Vilar, Rui; Beauverd, Yan; Aslan, D; ... Neerman Arbez, Marguerite
unige:112543	Thromboses veineuses splanchniques	Gouin, Bobby; Robert-Ebadi, Helia; Casini, Alessandro; Beauverd, Yan; ... Elkrief, Laure

2016

Scientific Articles

unige:85688	Can the phenotype of inherited fibrinogen disorders be predicted?	Casini, Alessandro; De Moerloose, Philippe;
unige:84424	Clinical Features and Management of Congenital Fibrinogen Deficiencies	Casini, Alessandro; De Moerloose, Philippe; Neerman Arbez, Marguerite;
unige:85853	Diagnostic des anomalies congénitales du fibrinogène	Lebreton, Aurélien; Casini, Alessandro;
unige:85686	Factor concentrates for rare congenital coagulation disorders: where are we now?	Casini, Alessandro; De Moerloose, Philippe;
unige:84427	Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders	Neerman Arbez, Marguerite; De Moerloose, Philippe; Casini, Alessandro;
unige:88364	Management of congenital quantitative fibrinogen disorders: a Delphi consensus	Casini, Alessandro; De Moerloose, Philippe;
unige:87658	Risks of venous thromboembolism after cesarean sections: A meta-analysis	Blondon, Marc; Casini, Alessandro; Hoppe, Kara K; Boehlen, Françoise; ... Smith, Nicholas L

Book Chapters

unige:88373	Congenital Disorders of Fibrinogen: Clinical Presentations, Diagnosis and Management	Casini, Alessandro; De Moerloose, Philippe;
unige:88374	Pregnancy	Marchetti, T; De Moerloose, Philippe; Casini, Alessandro;

2015

Scientific Articles

unige:79937	Comparing Two Types of Rabbit ATG prior to Reduced Intensity Conditioning Allogeneic Hematopoietic SCT for Hematologic Malignancies	Paiano, Sandra; Roosnek, Eddy Emile; Tirefort, Yordanka; Nagy-Hulliger, Monika; ... Chalandon, Yves
unige:83344	Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management	Casini, Alessandro; Neerman Arbez, Marguerite; Ariëns, R A; De Moerloose, Philippe;
unige:78669	Fibrin clot structure in patients with congenital dysfibrinogenaemia	Casini, Alessandro; Duval, C; Pan, X; Tintillier, V; ... Ariëns, R A S
unige:83345	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
unige:45599	Natural history of patients with congenital dysfibrinogenemia	Casini, Alessandro; Blondon, Marc; Lebreton, Aurelien; Koegel, Jeremie; ... De Moerloose, Philippe
unige:85687	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

Doctoral Thesis

unige:75217

Maladies héréditaires du fibrinogène: de la biologie moléculaire à la clinique

Casini, Alessandro;

2014

Scientific Articles

unige:39382	FGB mutations leading to congenital quantitative fibrinogen deficiencies: an update and report of four novel mutations	Casini, Alessandro; Lukowski, Samuel; Quintard, V Louvain; Crutu, A; ... Neerman Arbez, Marguerite
unige:39922	Fibrinogen geneva II: a new congenitally abnormal fibrinogen alpha chain (Gly17Asp) with a review of similar mutations resulting in abnormal knob A.	Casini, Alessandro; De Maistre, Emmanuel; Casini-Stuppi, Virginie; Fontana, Pierre; ... De Moerloose, Philippe
unige:34822	Hémostase. Aspirine: une ou deux fois par jour?	Fontana, Pierre; Casini, Alessandro; Boehlen, Françoise; Reny, Jean-Luc;
unige:55239	Validation of the disease risk index for outcome of patients undergoing allogeneic hematopoietic stem cell transplantation after T cell depletion	Beauverd, Yan; Roosnek, Eddy Emile; Tirefort, Yordanka; Nagy, Monika; ... Chalandon, Yves

2013

Scientific Articles

unige:78248	Acquired factor XIII deficiency: a therapeutic challenge	Boehlen, Françoise; Casini, Alessandro; Chizzolini, Carlo; Mansouri, Behrouz; ... De Moerloose, Philippe
unige:30893	Congenital fibrinogen disorders: an update	De Moerloose, Philippe; Casini, Alessandro; Neerman Arbez, Marguerite;