Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management
Casini, A., Neerman‐Arbez, M., Ariëns, R. A., Moerloose, P.
Published in Journal of thrombosis and haemostasis (01.06.2015)
Published in Journal of thrombosis and haemostasis (01.06.2015)
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Journal Article
Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation
Casini, A., Brungs, T., Lavenu‐Bombled, C., Vilar, R., Neerman‐Arbez, M., Moerloose, P.
Published in Journal of thrombosis and haemostasis (01.05.2017)
Published in Journal of thrombosis and haemostasis (01.05.2017)
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Journal Article
Local chromatin interactions contribute to expression of the fibrinogen gene cluster
Espitia Jaimes, C., Fish, R. J., Neerman‐Arbez, M.
Published in Journal of thrombosis and haemostasis (01.10.2018)
Published in Journal of thrombosis and haemostasis (01.10.2018)
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Journal Article
Afibrinogenemia with two compound heterozygous mutations in FGA gene
Feugray, Guillaume, Billoir, Paul, Casini, Alessandro, Neerman‐Arbez, M., Barbay, Virginie, Chamouni, Pierre, Schneider, Pascale, Le Cam Duchez, Véronique
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.09.2021)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.09.2021)
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Journal Article
Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature
Casini, A., Sokollik, C., Lukowski, S. W., Lurz, E., Rieubland, C., de Moerloose, P., Neerman-Arbez, M.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.11.2015)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.11.2015)
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Journal Article
Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia
Casini, A., Vilar, R., Beauverd, Y., Aslan, D., Devreese, K., Mondelaers, V., Alberio, L., Gubert, C., Moerloose, P., Neerman‐Arbez, M.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2017)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.07.2017)
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Journal Article
Successful pregnancy under fibrinogen substitution in a woman with congenital afibrinogenaemia complicated by a postpartum venous thrombosis
Lebreton, A., Casini, A., Alhayek, R., Kouteich, K. L., Neerman-Arbez, M., de Moerloose, P.
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.01.2015)
Published in Haemophilia : the official journal of the World Federation of Hemophilia (01.01.2015)
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Journal Article
FGB mutations leading to congenital quantitative fibrinogen deficiencies: An update and report of four novel mutations
Casini, A, Lukowski, S, Quintard, V. Louvain, Crutu, A, Zak, M, Regazzoni, S, de Moerloose, P, Neerman-Arbez, M
Published in Thrombosis research (01.05.2014)
Published in Thrombosis research (01.05.2014)
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Journal Article
In vitro rescue of FGA deletion by lentiviral transduction of an afibrinogenemic patient's hepatocytes
Stroka, D., Keogh, A., Vu, D., Fort, A., Stoffel, M. H., Kühni‐Boghenbor, K., Furer, C., Banz, V., Demarmels Biasiutti, F., Lämmle, B., Candinas, D., Neerman‐Arbez, M.
Published in Journal of thrombosis and haemostasis (01.11.2014)
Published in Journal of thrombosis and haemostasis (01.11.2014)
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Journal Article
Coexisting dysfibrinogenemia (γArg275His) and FV Leiden associated with thrombosis (Fibrinogen Crete)
Travlou, A, Gialeraki, A, Merkouri, E, Politou, M, Sfyridaki, A, Neerman-Arbez, M
Published in Thrombosis research (01.08.2010)
Published in Thrombosis research (01.08.2010)
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Journal Article
Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia : novel truncating mutations in the FGA and FGG genes
NEERMAN-ARBEZ, M, DE MOERLOOSE, P, RIPOLL, L, VERVEL, C, D'OIRON, R, STAEGER, P, ANTONARAKIS, S. E, MORRIS, M. A, HONSBERGER, A, PARLIER, G, ARNUTI, B, BIRON, C, BORG, J.-Y, EBER, S, MEILI, E, PETER-SALONEN, K
Published in Human genetics (01.03.2001)
Published in Human genetics (01.03.2001)
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Journal Article
A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream
Robert-Ebadi, H, de Moerloose, P, El Khorassani, M, El Khattab, M, Neerman-Arbez, M
Published in Blood coagulation & fibrinolysis (01.07.2009)
Published in Blood coagulation & fibrinolysis (01.07.2009)
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Journal Article
Molecular Analysis of the ERGIC-53 Gene in 35 Families With Combined Factor V-Factor VIII Deficiency
Neerman-Arbez, M., Johnson, K.M., Morris, M.A., McVey, J.H., Peyvandi, F., Nichols, W.C., Ginsburg, D., Rossier, C., Antonarakis, S.E., Tuddenham, E.G.D.
Published in Blood (01.04.1999)
Published in Blood (01.04.1999)
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Journal Article
PB1205 In Vitro Analysis of Plasma Clots with 0.7 to 10.4 g/L Fibrinogen Concentration by Turbidity, Permeation and Laser Scanning Electron Microscopy
Marchi, R., Liaudet, N., Neerman-Arbez, M.
Published in Research and practice in thrombosis and haemostasis (01.10.2023)
Published in Research and practice in thrombosis and haemostasis (01.10.2023)
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