| | Title | Authors / Editors | Date |
|
unige:161681 |
Differential impact of tamoxifen and aromatase inhibitors on thrombin generation: the prospective HEMOBREAST cohort |
Blondon, Marc; Bodmer, Alexandre; Thouvenin, Laure; Lecompte, Thomas Pierre; ... Casini, Alessandro |
2022 |
|
unige:154131 |
Novel missense mutations affecting the structure of the conserved fibrinogen Bβ C-terminal domain cause congenital hypofibrinogenemia |
Bartolo, Raquel; Arbez, Maxime; Ferreira Vilar Da Silva, Rui Filipe; Szanto, Timea; ... Neerman Arbez, Marguerite |
2021 |
|
unige:154132 |
Illustrated state-of-the-art capsules of the ISTH 2020 congress |
Krishnaswamy, Sriram; Ageno, Walter; Arabi, Yaseen; Barbui, Tiziano; ... Undas, Anetta |
2021 |
|
unige:154133 |
A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family |
Guipponi, Michel; Masclaux, Frédéric; Sloan Bena, Frédérique; Di Sanza, Corinne; ... Neerman Arbez, Marguerite |
2021 |
|
unige:154138 |
Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature |
Zdziarska, Joanna; Wypasek, Ewa; Iwaniec, Teresa; Ferreira Vilar Da Silva, Rui Filipe; ... Undas, Anetta |
2021 |
|
unige:145696 |
Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutations |
Marchi Cappelletti, Rita; Ferreira Vilar Da Silva, Rui Filipe; Durual, Stéphane; Goodyer, Matthew; ... Casini, Alessandro |
2021 |
|
unige:151329 |
Whole blood thromboelastometry by ROTEM and thrombin generation by genesia according to the genotype and clinical phenotype in congenital fibrinogen disorders |
Szanto, Timea; Lassila, Riitta; Lemponen, Marja; Lehtinen, Elina; ... Casini, Alessandro |
2021 |
|
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:154136 |
Chemical modulators of fibrinogen production and their impact on venous thrombosis |
Ferreira Vilar Da Silva, Rui Filipe; Lukowski, Samuel; Garieri, Marco; Di Sanza, Corinne; ... Fish, Richard |
2021 |
|
unige:153346 |
Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia |
Casini, Alessandro; von Mackensen, Sylvia; Santoro, Cristina; Djambas Khayat, Claudia; ... De Moerloose, Philippe |
2021 |
|
unige:140144 |
Investigating and modulating the regulation of fibrinogen production |
Ferreira Vilar Da Silva, Rui Filipe |
2020 |
|
unige:139876 |
A novel frameshift mutation in the FGA gene (c.196 delT) leading to congenital afibrinogenemia |
Aydin Köker, Sultan; Köker, Alper; Neerman Arbez, Marguerite; Ö Tunçer, Gökçen; ... Coban, Yasemin |
2020 |
|
unige:143435 |
MicroRNA-126 is a regulator of platelet-supported thrombin generation |
Zapilko, Veronika; Fish, Richard; Garcia, Alix; Reny, Jean-Luc; ... Fontana, Pierre |
2020 |
|
unige:131189 |
Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype |
Simurda, Tomas; Casini, Alessandro; Stasko, Jan; Hudecek, Jan; ... Kubisz, Peter |
2020 |
|
unige:154135 |
Case report: unmasked inherited dysfibrinogenemia after everolimus therapy |
Merkulova, Alona A; Mitchell, Steven C; Merkulov, Sergei; Wolberg, Alisa S; ... Schmaier, Alvin H |
2020 |
|
unige:154137 |
A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasis |
Freire, Cristina; Fish, Richard; Ferreira Vilar Da Silva, Rui Filipe; Di Sanza, Corinne; ... Neerman Arbez, Marguerite |
2020 |
|
unige:145792 |
Recommendations on the use of anticoagulants for the treatment of patients with heparin-induced thrombocytopenia in Switzerland |
Alberio, Lorenzo; Angelillo-Scherrer, Anne; Asmis, Lars; Casini, Alessandro; ... Wuillemin, Walter |
2020 |
|
unige:142491 |
From Routine to Research Laboratory: Strategies for the Diagnosis of Congenital Fibrinogen Disorders |
Casini, Alessandro |
2020 |
|
unige:146958 |
A novel nonsense mutation in FBG (c.1421G>A;p.Trp474Ter) in the beta chain of fibrinogen causing hypofibrinogenemia with bleeding phenotype |
Simurda, Tomas; Ferreira Vilar Da Silva, Rui Filipe; Zolkova, Jana; Ceznerova, Eliska; ... Kubisz, Peter |
2020 |
|
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 |
Recherche translationnelle : anomalies de l'hémostase et thromboses (504)
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