| | Title | Authors / Editors | Date |
|
unige:151331 |
Comparison of different activators of coagulation by turbidity analysis of hereditary dysfibrinogenemia and controls |
Marchi Cappelletti, Rita; Neerman Arbez, Marguerite; Gay, Valérie; Mourey, Guillaume; ... Casini, Alessandro |
2021 |
|
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 |
2020 |
|
unige:151332 |
Heterogeneity of congenital afibrinogenemia, from epidemiology to clinical consequences and management |
Casini, Alessandro; Neerman Arbez, Marguerite; De Moerloose, Philippe |
2020 |
|
unige:127885 |
Fibrinogen concentrates in hereditary fibrinogen disorders: past, present and future |
Casini, Alessandro; De Moerloose, Philippe |
2019 |
|
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 |
2019 |
|
unige:125939 |
Impaired factor XIII activation in patients with congenital afibrinogenemia |
Bridey, Françoise; Négrier, Claude; Duval, Cedric; Ariëns, Robert; ... Casini, Alessandro |
2019 |
|
unige:115121 |
Mutational epidemiology of congenital fibrinogen disorders |
Casini, Alessandro; Blondon, Marc; Tintillier, Veronique; Goodyer, Matthew; ... Neerman Arbez, Marguerite |
2018 |
|
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: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: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: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:99478 |
Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia |
Casini, Alessandro; Vilar, Rui; Beauverd, Yan; Aslan, D; ... Neerman Arbez, Marguerite |
2017 |
|
unige:88364 |
Management of congenital quantitative fibrinogen disorders: a Delphi consensus |
Casini, Alessandro; De Moerloose, Philippe |
2016 |
|
unige:89769 |
Preoperative hemostatic assessment: a new and simple bleeding questionnaire |
Bonhomme, Fanny; Boehlen, Françoise; Clergue, François; 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:85686 |
Factor concentrates for rare congenital coagulation disorders: where are we now? |
Casini, Alessandro; De Moerloose, Philippe |
2016 |
De Moerloose, Philippe
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