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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 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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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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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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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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Combined factor V - factor VIII deficiency (F5F8D): compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patient Farah, R. A.; De Moerloose, Philippe; Bouchardy, Isabelle; Morris, Michael Andréw; ... Neerman Arbez, Marguerite 2006
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Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion Vu, Dung; Bolton-Maggs, P. H.; Parr, J. R.; Morris, Michael Andréw; ... Neerman Arbez, Marguerite 2003
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Congenital fibrinogen disorders De Moerloose, Philippe; Neerman Arbez, Marguerite 2009
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Congenital fibrinogen disorders: an update De Moerloose, Philippe; Casini, Alessandro; Neerman Arbez, Marguerite 2013
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Cryptic splice site usage leading to truncated TMPRSS6 is responsible for iron refractory iron deficiency anaemia in an Italian Family Tchou, Isabelle; Neerman Arbez, Marguerite; Beris, Photis 2011
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Decreased plasmin resistance by clots of a homophenotypic Aalpha R 16H fibrinogen (Kingsport, slower fibrinopeptide A than fibrinopeptide B release) Galanakis, D. K.; Neerman Arbez, Marguerite; Kudryk, Bohdan; Henschen, Agnes 2010
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Deletion of 3 residues from the C-terminus of MCFD2 affects binding to ERGIC-53 and causes combined factor V and factor VIII deficiency Nyfeler, Beat; Kamiya, Yukiko; Boehlen, Françoise; Yamamoto, Kazuo; ... Neerman Arbez, Marguerite 2008
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