Marguerite Neerman-Arbez

Papers authored by Marguerite Neerman-Arbez

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2006 M. Neerman-Arbez

Molecular Basis of Fibrinogen Deficiency

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Roula A. Farah, Philippe de Moerloose, Isabelle Bouchardy, Michael A. Morris, Wadad Barakat, Alain E. Sayad, Marguerite Neerman-Arbez

Combined factor V – factor VIII deficiency (F5F8D): Compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patient

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2005 Corinne Di Sanza, Dung Vu, Dorothée Caille, Philippe de Moerloose, Holger Scheib, Paolo Meda, Marguerite Neerman-Arbez

Quality control of fibrinogen secretion in the molecular pathogenesis of congenital afibrinogenemia

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Myrna Germanos-Haddad, Philippe de Moerloose, Françoise Boehlen, Flora Peyvandi, Marguerite Neerman-Arbez

Homozygosity for a Thr575Met missense mutation in the catalytic domain associated with factor XI deficiency

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2004 Myrna Germanos-Haddad, Marguerite Neerman-Arbez

, Konstantinos Tzanidakis, Dung Vu, Samuel Deutsch, Armelle David, Philippe de Moerloose, Michael A. Morris

Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: Escape from RNA surveillance mechanisms in transfected cells

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Philippe de Moerloose, Myrna Germanos-Haddad, Françoise Boehlen, Marguerite Neerman-Arbez

Severe factor XI deficiency in a Lebanese family

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2003 Paula H. B. Bolton Maggs, Dung Vu, Jeremy R. Parr, Michael A. Morris, Philippe de Moerloose, Marguerite Neerman-Arbez

Congenital afibrinogenemia: Identification and expression of a missense mutation in FGB impairing fibrinogen secretion

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Marc Friedli, Michel Guipponi, Sonia Bertrand, Daniel Bertrand, Marguerite Neerman-Arbez

, Hamish S. Scott

, Stylianos E. Antonarakis, Alexandre Reymond

Identification of a novel member of the CLIC family, CLIC6, mapping to 21q22.12

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Marguerite Neerman-Arbez

, Dung Vu, Bassam Abu-Libdeh, Isabelle Bouchardy, Michael A. Morris

Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family

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2002 Catia Attanasio, Armelle David, Marguerite Neerman-Arbez

Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA)

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2001 Marguerite Neerman-Arbez

Fibrinogen Gene Mutations Accounting for Congenital Afibrinogenemia

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M. Neerman-Arbez

, P. de Moerloose, A. Honsberger, G. Parlier, B. Arnuti, C. Biron, J.-Y. Borg, S. Eber, E. Meili, K. Peter-Salonen, L. Ripoll, C. Vervel, R. d' Oiron, P. Staeger, S. Antonarakis and 1 other authors

Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes

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Catia Attanasio, Philippe de Moerloose, Stylianos E. Antonarakis, Michael A. Morris, Marguerite Neerman-Arbez

Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4 + 1 G→T

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Marguerite Neerman-Arbez

The Molecular Basis of Inherited Afibrinogenaemia

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2000 M. Neerman Arbez

, P. de Moerloose, C. Bridel, A. Honsberger, A. Schönbörner, C. Rossier, K. Peerlinck, S. Claeyssens, D. Di Michele, R. d'Oiron, M. Dreyfus, Morris Ma

Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.

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1999 Marguerite Neerman-Arbez

, Stylianos E. Antonarakis, Ariane Honsberger, Michael A. Morris

The 11 kb FGA deletion responsible for congenital afibrinogenaemia is mediated by a short direct repeat in the fibrinogen gene cluster

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M. Neerman-Arbez

, Nichols Wc, K. M. Johnson, Johnson Km, Morris Ma, M. A. Morris, McVey Jh, J. H. McVey, F. Peyvandi, W. C. Nichols, D. Ginsburg, C. Rossier, S. E. Antonarakis, Antonarakis Se, Tuddenham Eg and 1 other authors

Molecular Analysis of the ERGIC-53 Gene in 35 Families With Combined Factor V-Factor VIII Deficiency

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M. Neerman Arbez

, A. Honsberger, Antonarakis Se, Morris Ma

Deletion of the fibrinogen alpha-chain gene () causes congenital afibrogenemia.

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Marguerite Neerman-Arbez

, Ariane Honsberger, Stylianos E. Antonarakis, Michael A. Morris

Deletion of the fibrogen alpha-chain gene (FGA) causes congenital afibrogenemia

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1997 M. Neerman-Arbez

, S. E. Antonarakis, J.-L. Blouin, S. Zeinali, M. Akhtari, Y. Afshar, E. G. D. Tuddenham