Page 1 | Search Results | Blood | American Society of Hematology

1-15 of 15

Sort by

Sort Order Select

Journal Articles

When fibrin(ogen) is too loud, silence it!

Marguerite Neerman-Arbez

Blood (2022) 139 (9): 1261–1262.

https://doi.org/10.1182/blood.2021015215

Published: 2022

Journal Articles

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

Ilenia Simeoni, Jonathan C. Stephens, Fengyuan Hu, Sri V. V. Deevi, Karyn Megy, Tadbir K. Bariana, Claire Lentaigne, Sol Schulman, Suthesh Sivapalaratnam, Minka J. A. Vries, Sarah K. Westbury, Daniel Greene, Sofia Papadia, Marie-Christine Alessi, Antony P. Attwood, Matthias Ballmaier, Gareth Baynam, Emilse Bermejo, Marta Bertoli, Paul F. Bray, Loredana Bury, Marco Cattaneo, Peter Collins, Louise C. Daugherty, Rémi Favier, Deborah L. French, Bruce Furie, Michael Gattens, Manuela Germeshausen, Cedric Ghevaert, Anne C. Goodeve, Jose A. Guerrero, Daniel J. Hampshire, Daniel P. Hart, Johan W. M. Heemskerk, Yvonne M. C. Henskens, Marian Hill, Nancy Hogg, Jennifer D. Jolley, Walter H. Kahr, Anne M. Kelly, Ron Kerr, Myrto Kostadima, Shinji Kunishima, Michele P. Lambert, Ri Liesner, José A. López, Rutendo P. Mapeta, Mary Mathias, Carolyn M. Millar, Amit Nathwani, Marguerite Neerman-Arbez, Alan T. Nurden, Paquita Nurden, Maha Othman, Kathelijne Peerlinck, David J. Perry, Pawan Poudel, Pieter Reitsma, Matthew T. Rondina, Peter A. Smethurst, William Stevenson, Artur Szkotak, Salih Tuna, Christel van Geet, Deborah Whitehorn, David A. Wilcox, Bin Zhang, Shoshana Revel-Vilk, Paolo Gresele, Daniel B. Bellissimo, Christopher J. Penkett, Michael A. Laffan, Andrew D. Mumford, Augusto Rendon, Keith Gomez, Kathleen Freson, Willem H. Ouwehand, Ernest Turro

Blood (2016) 127 (23): 2791–2803.

https://doi.org/10.1182/blood-2015-12-688267

Published: 2016

Includes: Supplemental data

Journal Articles

Natural history of patients with congenital dysfibrinogenemia

Alessandro Casini, Marc Blondon, Aurélien Lebreton, Jérémie Koegel, Véronique Tintillier, Emmanuel de Maistre, Philippe Gautier, Christine Biron, Marguerite Neerman-Arbez, Philippe de Moerloose

Blood (2015) 125 (3): 553–561.

https://doi.org/10.1182/blood-2014-06-582866

Published: 2015

Includes: Supplemental data

Journal Articles

Targeted mutation of zebrafish fga models human congenital afibrinogenemia

Richard J. Fish, Corinne Di Sanza, Marguerite Neerman-Arbez

Blood (2014) 123 (14): 2278–2281.

https://doi.org/10.1182/blood-2013-12-547182

Published: 2014

Includes: Supplemental data

Journal Articles

A liver enhancer in the fibrinogen gene cluster

Alexandre Fort, Richard J. Fish, Catia Attanasio, Roland Dosch, Axel Visel, Marguerite Neerman-Arbez

Blood (2011) 117 (1): 276–282.

https://doi.org/10.1182/blood-2010-07-295410

Published: 2011

Includes: Supplemental data

Journal Articles

Regulation of fibrinogen production by microRNAs

Alexandre Fort, Christelle Borel, Eugenia Migliavacca, Stylianos E. Antonarakis, Richard J. Fish, Marguerite Neerman-Arbez

Blood (2010) 116 (14): 2608–2615.

https://doi.org/10.1182/blood-2010-02-268011

Published: 2010

Includes: Supplemental data

Journal Articles

Enhanced Fibrinolysis of Coarse Fibrin Networks Reflects Cleavage of a B Knob Containing Fragment(s)

Dennis K. Galanakis, MD, Marguerite Neerman-Arbez, Ph.D, Agnes Henschen, Bodan Kudryk, Ph.D

Blood (2008) 112 (11): 1019.

https://doi.org/10.1182/blood.V112.11.1019.1019

Published: 2008

Journal Articles

Deletion of 3 residues from the C-terminus of MCFD2 affects binding to ERGIC-53 and causes combined factor V and factor VIII deficiency

Beat Nyfeler, Yukiko Kamiya, Françoise Boehlen, Kazuo Yamamoto, Koichi Kato, Philippe de Moerloose, Hans-Peter Hauri, Marguerite Neerman-Arbez

Blood (2008) 111 (3): 1299–1301.

https://doi.org/10.1182/blood-2007-09-112854

Published: 2008

Journal Articles

Genetic and Phenotypic Analysis of Families with Inherited Hypo- and Dys-Fibrinogenemia. Fibrinogen Bratislava.

Angelika Batorova, MD, PhD, Daniela Horvathova, MD, Martin Mistrik, MD, PhD, Philippe de Moerloose, MD, PhD, Marguerite Neerman-Arbez, MD, PhD

Blood (2005) 106 (11): 1794.

https://doi.org/10.1182/blood.V106.11.1794.1794

Published: 2005

Journal Articles

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

Marguerite Neerman-Arbez, Myrna Germanos-Haddad, Konstantinos Tzanidakis, Dung Vu, Samuel Deutsch, Armelle David, Michael A. Morris, Philippe de Moerloose

Blood (2004) 104 (12): 3618–3623.

https://doi.org/10.1182/blood-2004-06-2312

Published: 2004

Journal Articles

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

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

Blood (2003) 102 (13): 4413–4415.

https://doi.org/10.1182/blood-2003-06-2141

Published: 2003

Journal Articles

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

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

Blood (2003) 101 (9): 3492–3494.

https://doi.org/10.1182/blood-2002-10-3116

Published: 2003

Journal Articles

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

Catia Attanasio, Armelle David, Marguerite Neerman-Arbez

Blood (2003) 101 (5): 1851–1856.

https://doi.org/10.1182/blood-2002-03-0853

Published: 2003

Journal Articles

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

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

Blood (2001) 97 (6): 1879–1881.

https://doi.org/10.1182/blood.V97.6.1879

Published: 2001

Journal Articles

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

Marguerite Neerman-Arbez, Philippe de Moerloose, Claire Bridel, Ariane Honsberger, Anni Schönbörner, Colette Rossier, Kathelijne Peerlinck, Ségolène Claeyssens, Donna Di Michele, Roseline d'Oiron, Marie Dreyfus, Monique Laubriat-Bianchin, Jacelyne Dieval, Stylianos E. Antonarakis, Michael A. Morris

Blood (2000) 96 (1): 149–152.

https://doi.org/10.1182/blood.V96.1.149

Published: 2000

NARROW

When fibrin(ogen) is too loud, silence it!

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

Natural history of patients with congenital dysfibrinogenemia

Targeted mutation of zebrafish fga models human congenital afibrinogenemia

A liver enhancer in the fibrinogen gene cluster

Regulation of fibrinogen production by microRNAs

Enhanced Fibrinolysis of Coarse Fibrin Networks Reflects Cleavage of a B Knob Containing Fragment(s)

Deletion of 3 residues from the C-terminus of MCFD2 affects binding to ERGIC-53 and causes combined factor V and factor VIII deficiency

Genetic and Phenotypic Analysis of Families with Inherited Hypo- and Dys-Fibrinogenemia. Fibrinogen Bratislava.

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

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

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

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

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

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

Email alerts

ASH Publications

American Society of Hematology

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only