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	Title	Authors / Editors	Date
unige:106807	Prevalence, persistence and clinical correlations of classic and novel antiphospholipid antibodies in systemic lupus erythematosus	Marchetti, Tess; Ribi, Camillo; Perneger, Thomas; Trendelenburg, Marten; ... Chizzolini, Carlo	2018
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	2018
unige:92556	A multicenter study to assess the reproducibility of antiphospholipid antibody results produced by an automated system	Devreese, K M; Poncet, Antoine; Lindhoff-Last, E; Musial, J; ... Fontana, Pierre	2017
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	2017
unige:99478	Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia	Casini, Alessandro; Vilarino, Raquel; Beauverd, Yan; Aslan, D; ... Neerman Arbez, Marguerite	2017
unige:100208	Patient-derived anti-β2GP1 antibodies recognize a peptide motif pattern and not a specific sequence of residues	De Moerloose, Philippe; Fickentscher, Céline; Boehlen, Françoise; Tiercy, Jean-Marie; ... Brandt, Karim J	2017
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	2017
unige:88364	Management of congenital quantitative fibrinogen disorders: a Delphi consensus	Casini, Alessandro; De Moerloose, Philippe	2016
unige:88373	Congenital Disorders of Fibrinogen: Clinical Presentations, Diagnosis and Management	Casini, Alessandro; De Moerloose, Philippe	2016
unige:88374	Pregnancy	Marchetti, T; De Moerloose, Philippe; Casini, Alessandro	2016
unige:86248	F-actin dampens NLRP3 inflammasome activity via Flightless-I and LRRFIP2	Burger, Danielle; Fickentscher, Céline; De Moerloose, Philippe; Brandt, Karim	2016
unige:89769	Preoperative hemostatic assessment: a new and simple bleeding questionnaire	Bonhomme, Fanny; Boehlen, Françoise; Clergue, François; De Moerloose, Philippe	2016
unige:85688	Can the phenotype of inherited fibrinogen disorders be predicted?	Casini, Alessandro; De Moerloose, Philippe	2016
unige:84424	Clinical Features and Management of Congenital Fibrinogen Deficiencies	Casini, Alessandro; De Moerloose, Philippe; Neerman Arbez, Marguerite	2016
unige:84427	Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders	Neerman Arbez, Marguerite; De Moerloose, Philippe; Casini, Alessandro	2016
unige:85686	Factor concentrates for rare congenital coagulation disorders: where are we now?	Casini, Alessandro; De Moerloose, Philippe	2016
unige:112230	Hypertension, haematuria and renal functioning in haemophilia - a cross-sectional study in Europe	Holme, P. A.; Combescure, Christophe; Tait, R.C.; Berntorp, E.; ... De Moerloose, Philippe	2016
unige:89774	Recombinant human FVIIa for reducing the need for invasive second-line therapies in severe refractory postpartum hemorrhage: a multicenter, randomized, open controlled trial	Lavigne-Lissalde, G; Aya, A G; Mercier, F J; Roger-Christoph, S; ... Gris, J-C	2015
unige:45599	Natural history of patients with congenital dysfibrinogenemia	Casini, Alessandro; Blondon, Marc; Lebreton, Aurelien; Koegel, Jeremie; ... De Moerloose, Philippe	2015
unige:83344	Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management	Casini, Alessandro; Neerman Arbez, Marguerite; Ariëns, R A; De Moerloose, Philippe	2015

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