2018

Scientific Articles

unige:101803

Clinical Consequences and Molecular Bases of Low Fibrinogen Levels

Neerman Arbez, Marguerite; Casini, Alessandro;

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; Vilarino, Raquel; Beauverd, Yan; Aslan, D; ... Neerman Arbez, Marguerite

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;
unige:89772	Hémostase : nouveaux anticoagulants oraux : de la théorie à la pratique	De Moerloose, Philippe; Casini, Alessandro; Boehlen, Françoise; Fontana, Pierre;
unige:85684	Pulmonary embolism and fatal stroke in a patient with severe factor XI deficiency after bariatric surgery	Boehlen, Françoise; Casini, Alessandro; Pugin, François Louis; De Moerloose, Philippe;
unige:29635	Thrombotic complications of myeloproliferative neoplasms: risk assessment and risk-guided management	Casini, Alessandro; Fontana, Pierre; Lecompte, Thomas Pierre;

Book Chapters

unige:88377

Could Factor XIII be a solution for the management of surgical bleeding?

Casini, Alessandro; De Moerloose, Philippe;

2012

Scientific Articles

unige:85685

Thrombophilie : quel bilan en 2012?

De Moerloose, Philippe; Casini, Alessandro; Boehlen, Françoise;

2011

Scientific Articles

unige:24268

Recurrent Syncope due to Esophageal Squamous Cell Carcinoma

Casini, Alessandro; Tschanz, Elisabeth; Dietrich, Pierre-Yves; Nendaz, Mathieu;