RF
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Title Published in Access level OA Policy Year Views Downloads
Novel missense mutations affecting the structure of the conserved fibrinogen Bβ C-terminal domain cause congenital hypofibrinogenemiaThrombosis Research
accessLevelPublic
2021 211 163
Fibrin clot properties to assess the bleeding phenotype in unrelated patients with hypodysfibrinogenemia due to novel fibrinogen mutationsThrombosis Research
accessLevelRestricted
2021 584 4
Chemical modulators of fibrinogen production and their impact on venous thrombosisThrombosis and Haemostasis
accessLevelPublic
2021 264 227
Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literatureHaemophilia
accessLevelPublic
2021 229 383
Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotypeThrombosis Research
accessLevelPublic
2020 362 48
Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia AThrombosis Research
accessLevelRestricted
2020 270 2
Fibrin(ogen) in human disease: both friend and foeHaematologica
accessLevelPublic
2020 479 338
A novel nonsense mutation in FBG (c.1421G>A;p.Trp474Ter) in the beta chain of fibrinogen causing hypofibrinogenemia with bleeding phenotypeBiomedicines
accessLevelPublic
2020 280 150
Investigating and modulating the regulation of fibrinogen production
accessLevelRestricted
2020 542 16
A genetic modifier of venous thrombosis in zebrafish reveals a functional role for fibrinogen AαE in early hemostasisBlood Advances
accessLevelPublic
2020 214 195
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