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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
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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
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A liver enhancer in the fibrinogen gene cluster Fort, Alexandre; Fish, Richard; Attanasio, Catia; Dosch, Roland; ... Neerman Arbez, Marguerite 2011
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A novel Asp344Val substitution in the fibrinogen gamma chain (fibrinogen Caen) causes dysfibrinogenemia associated with thrombosis Robert-Ebadi, Helia; Le Querrec, Agnès; De Moerloose, Philippe; Gandon-Laloum, Sylvie; ... Neerman Arbez, Marguerite 2008
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A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family Levrat, Emmanuel; Aboukhamis, Imad; De Moerloose, Philippe; Farho, Jaafar; ... Neerman Arbez, Marguerite 2011
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A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream Robert-Ebadi, Helia; De Moerloose, Philippe; El Khorassani, M.; El Khattab, M.; Neerman Arbez, Marguerite 2009
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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
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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
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A novel regulatory element between the human FGA and FGG genes Fish, Richard; Neerman Arbez, Marguerite 2012
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Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T Attanasio, Catia; De Moerloose, Philippe; Antonarakis, Stylianos; Morris, Michael Andréw; Neerman Arbez, Marguerite 2001
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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
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Afibrinogénémie congénitale et contrôle de qualité de la sécrétion du fibrinogène Vu, Dung; Neerman Arbez, Marguerite 2006
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Apprentissage par problèmes des sciences médicales de base : les années précliniques (Bachelor) Baroffio Barbier, Anne; Neerman Arbez, Marguerite; Gallay, Christophe; Bernheim, Laurent 2011
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C2orf62 and TTC17 are involved in actin organization and ciliogenesis in zebrafish and human Bontems, Franck; Fish, Richard; Rossitto-Borlat, Irène; Lembo, Frédérique; ... Lane, Lydie 2014
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Case report: unmasked inherited dysfibrinogenemia after everolimus therapy Merkulova, Alona A; Mitchell, Steven C; Merkulov, Sergei; Wolberg, Alisa S; ... Schmaier, Alvin H 2020
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Characterisation of a novel nonsense mutation in FGG (Fibrinogen Poznan) causing hypofibrinogenaemia with a mild bleeding tendency Zawilska, Krystyna; Undas, Anetta; Fish, R. J.; Molendowicz-Portala, Lucyna; ... Neerman Arbez, Marguerite 2010
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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
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Clinical Consequences and Molecular Bases of Low Fibrinogen Levels Neerman Arbez, Marguerite; Casini, Alessandro 2018
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Clinical Features and Management of Congenital Fibrinogen Deficiencies Casini, Alessandro; De Moerloose, Philippe; Neerman Arbez, Marguerite 2016
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Coexisting dysfibrinogenemia (gamma Arg275His) and FV Leiden associated with thrombosis (Fibrinogen Crete) Travlou, A.; Gialeraki, A.; Merkouri, E.; Politou, M.; ... Neerman Arbez, Marguerite 2010
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