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Journal Articles

Safety and Efficacy of Fibrinogen Concentrate in Congenital Fibrinogen Deficiency: A Post-Marketing Observational Study

Bruce A. Schwartz, PhD, Flora Peyvandi, MD PhD, Cristina Solomon, Sigurd Knaub, Balazs Toth

Blood (2019) 134 (Supplement_1): 4971.

https://doi.org/10.1182/blood-2019-129891

Published: 2019

Journal Articles

Efficacy and Pharmacokinetics of a New Fibrinogen Concentrate in Treating Acute Bleeding in Adolescent Patients with Congenital Fibrinogen Deficiency

Flora Peyvandi, MD PhD, Bruce A. Schwartz, Sigurd Knaub

Blood (2018) 132 (Supplement 1): 2501.

https://doi.org/10.1182/blood-2018-99-116572

Published: 2018

Journal Articles

Efficacy and Safety of Fibrinogen Concentrate for on-Demand Treatment of Acute Bleeding and for Surgical Prophylaxis in Subjects with Congenital Fibrinogen Deficiency — a Phase 3 Study

Flora Peyvandi, MD PhD, Bruce A. Schwartz, Sigurd Knaub

Blood (2018) 132 (Supplement 1): 2502.

https://doi.org/10.1182/blood-2018-99-116440

Published: 2018

Journal Articles

Efficacy of Human Fibrinogen Concentrate for on-Demand Treatment of Acute Bleeding and to Prevent Bleeding during and after Surgery in Subjects with Congenital Fibrinogen Deficiency

Bruce A. Schwartz, PhD, Cecil Ross, MD, Bella Madan, MD, Toshko Jelev Lissitchkov, MD, Mehran Karimi, MD, Sigurd Knaub, Flora Peyvandi, MD PhD

Blood (2016) 128 (22): 1404.

https://doi.org/10.1182/blood.V128.22.1404.1404

Published: 2016

Journal Articles

Screening Method for Hepatic Fibrinogen Storage Disease Associated with Congenital Hypofibrinogenemia

Shinpei Arai, MS, Saki Mukai, BA, Yuka Takezawa, PhD, Mitsutoshi Sugano, PhD, Takayuki Honda, MD PhD, Fumihiro Ishida, MD PhD, Nobuo Okumura, PhD

Blood (2015) 126 (23): 3504.

https://doi.org/10.1182/blood.V126.23.3504.3504

Published: 2015

Journal Articles

Pharmacokinetic (PK) Comparison of Two Fibrinogen Concentrates in Patients with Congenital Fibrinogen Deficiency: Final Analysis

Cecil Ross, MD, Savita Rangarajan, Mehran Karimi, MD, Bruce A. Schwartz, PhD, Sigurd Knaub, PhD, Flora Peyvandi, MD PhD

Blood (2015) 126 (23): 4680.

https://doi.org/10.1182/blood.V126.23.4680.4680

Published: 2015

Journal Articles

Identification of Novel Mutations with Molecular Modelling of Missense Mutations of Congenital Afibrinogenemia Patients in Pakistan

Tehmina nafees sonia Khan, M.B;B.S ,PhD, Arshi Naz, MSc.PhD, Arjit Biswas, Anne Goodeve, PhD, Nisar Ahmed, FCPS haematology, Shariq Ahmed, B.S, Tahir Shamsi, MBBS, MRCPath,FRCPath, Johannes Oldenburg

Blood (2015) 126 (23): 4664.

https://doi.org/10.1182/blood.V126.23.4664.4664

Published: 2015

Journal Articles

Characterization of Phenotypic Expression of Inherited Fibrinogen Coagulopathy in Pakistani Index Patients

Arshi Naz, MSc.PhD, Tehmina nafees sonia Khan, M.B;B.S ,PhD, Noman A Malik, M.B.B.S. (Pb) , M. Phil., Shahla Tariq, M.B;B.S, Nazish Saqlain, FCPS haematology, Tahir Shamsi, MBBS, MRCPath,FRCPath

Blood (2015) 126 (23): 4667.

https://doi.org/10.1182/blood.V126.23.4667.4667

Published: 2015

Journal Articles

Pharmacokinetic (PK) Comparison of Two Fibrinogen Concentrates for the Treatment of Congenital Fibrinogen Deficiency

Bruce A. Schwartz, PhD, Savita Rangarajan, MBBS, FRCP, FRCPath, Flora Peyvandi, Mehran Karimi, MD, Sigurd Knaub, PhD

Blood (2014) 124 (21): 2817.

https://doi.org/10.1182/blood.V124.21.2817.2817

Published: 2014

Journal Articles

Severe Spontaneous Intracranial Bleeding in 11 Months Old Boy with Congenital Afibrinogenemia with Novel Mutation - Deletion aα 6477A in Fibrinogen Gene

Ondrej Zapletal, MD PhD, Jan Blatny, MD PhD, Roman Kotlin, Jan E Dyr

Blood (2014) 124 (21): 5070.

https://doi.org/10.1182/blood.V124.21.5070.5070

Published: 2014

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

Treatment of Congenital Fibrinogen Deficiency; Global Development Plan for a Double Virus Inactivated Fibrinogen Concentrate

Bruce A. Schwartz, PhD, Sigurd Knaub, PhD

Blood (2012) 120 (21): 4636.

https://doi.org/10.1182/blood.V120.21.4636.4636

Published: 2012

Journal Articles

Afibrinogenemia: a Disorder of Paradoxical Bleeding and Clotting.

Mindy L. Grunzke, MD, Chris Bombardier, BS, Linda J. Jacobson, MT, Neil A. Goldenberg, MD, PhD, Marilyn J. Manco-Johnson, MD

Blood (2009) 114 (22): 3477.

https://doi.org/10.1182/blood.V114.22.3477.3477

Published: 2009

Journal Articles

Intracranial Haemorrhage in Patients with An Inherited Bleeding Disorder: A Review of 10 Years Experience in a UK Haemophilia Comprehensive Centre.

Siamak Arami, Tina T. Biss, Kate Talks

Blood (2009) 114 (22): 3489.

https://doi.org/10.1182/blood.V114.22.3489.3489

Published: 2009

Journal Articles

The Evaluation of a Prothrombotic Risk in a Human Fibrinogen Concentrate

Gerhard Dickneite, Christine Joch, Garrett E. Bergman, MD, MBA

Blood (2008) 112 (11): 4064.

https://doi.org/10.1182/blood.V112.11.4064.4064

Published: 2008

Journal Articles

Afibrinogenaemia Resulting from a Novel Putative Splicing Mutation, and Evidence for Tissue Specific Expression of FGAα RNA.

Jacky Cutler, Louise Bourdon, Geoffrey F. Savidge

Blood (2005) 106 (11): 2137.

https://doi.org/10.1182/blood.V106.11.2137.2137

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

NARROW

Safety and Efficacy of Fibrinogen Concentrate in Congenital Fibrinogen Deficiency: A Post-Marketing Observational Study

Efficacy and Pharmacokinetics of a New Fibrinogen Concentrate in Treating Acute Bleeding in Adolescent Patients with Congenital Fibrinogen Deficiency

Efficacy and Safety of Fibrinogen Concentrate for on-Demand Treatment of Acute Bleeding and for Surgical Prophylaxis in Subjects with Congenital Fibrinogen Deficiency — a Phase 3 Study

Efficacy of Human Fibrinogen Concentrate for on-Demand Treatment of Acute Bleeding and to Prevent Bleeding during and after Surgery in Subjects with Congenital Fibrinogen Deficiency

Screening Method for Hepatic Fibrinogen Storage Disease Associated with Congenital Hypofibrinogenemia

Pharmacokinetic (PK) Comparison of Two Fibrinogen Concentrates in Patients with Congenital Fibrinogen Deficiency: Final Analysis

Identification of Novel Mutations with Molecular Modelling of Missense Mutations of Congenital Afibrinogenemia Patients in Pakistan

Characterization of Phenotypic Expression of Inherited Fibrinogen Coagulopathy in Pakistani Index Patients

Pharmacokinetic (PK) Comparison of Two Fibrinogen Concentrates for the Treatment of Congenital Fibrinogen Deficiency

Severe Spontaneous Intracranial Bleeding in 11 Months Old Boy with Congenital Afibrinogenemia with Novel Mutation - Deletion aα 6477A in Fibrinogen Gene

Targeted mutation of zebrafish fga models human congenital afibrinogenemia

Treatment of Congenital Fibrinogen Deficiency; Global Development Plan for a Double Virus Inactivated Fibrinogen Concentrate

Afibrinogenemia: a Disorder of Paradoxical Bleeding and Clotting.

Intracranial Haemorrhage in Patients with An Inherited Bleeding Disorder: A Review of 10 Years Experience in a UK Haemophilia Comprehensive Centre.

The Evaluation of a Prothrombotic Risk in a Human Fibrinogen Concentrate

Afibrinogenaemia Resulting from a Novel Putative Splicing Mutation, and Evidence for Tissue Specific Expression of FGAα RNA.

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)

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American Society of Hematology

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American Society of Hematology

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