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Physiological correction of hereditary mild hypofibrinogenemia during pregnancy

Haemophilia : the official journal of the World Federation of Hemophilia, 2023-05, Vol.29 (3), p.836-843

2023

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Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: A systematic literature review

Haemophilia : the official journal of the World Federation of Hemophilia, 2019-09, Vol.25 (5), p.747-754

2019

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A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec

Haemophilia : the official journal of the World Federation of Hemophilia, 2024-05, Vol.30 (3), p.858-861

2024

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Hemizygous FGG p.Ala108Gly in a hypofibrinogenemic patient with a heterozygous 14.8 Mb deletion encompassing the entire fibrinogen gene cluster

Haemophilia : the official journal of the World Federation of Hemophilia, 2022-09, Vol.28 (5), p.e132-e135

2022

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Clinical Consequences and Molecular Bases of Low Fibrinogen Levels

International journal of molecular sciences, 2018-01, Vol.19 (1), p.192

2018

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Fibrin(ogen) in human disease: both friend and foe

Haematologica (Roma), 2020-02, Vol.105 (2), p.284

2020

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Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations

Human mutation, 2007-06, Vol.28 (6), p.540-553

2007

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Clinical Features and Management of Congenital Fibrinogen Deficiencies

Seminars in thrombosis and hemostasis, 2016-06, Vol.42 (4), p.366

2016

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Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders

Seminars in thrombosis and hemostasis, 2016-06, Vol.42 (4), p.356

2016

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Fibrinogen gene regulation

Thrombosis and haemostasis, 2012-09, Vol.108 (3), p.419

2012

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Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-01, Vol.27 (1), p.26-32

2021

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Cryptic splice site usage leading to truncated TMPRSS6 is responsible for iron refractory iron deficiency anaemia in an Italian Family

European journal of haematology, 2011-02, Vol.86 (2), p.178-179

2011

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Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders

International journal of molecular sciences, 2021-02, Vol.22 (5), p.2286

2021

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Venous Thrombosis and Thrombocyte Activity in Zebrafish Models of Quantitative and Qualitative Fibrinogen Disorders

International journal of molecular sciences, 2021-01, Vol.22 (2), p.655

2021

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Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations

Thrombosis research, 2019-10, Vol.182, p.133-140

2019

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Targeted mutation of zebrafish fga models human congenital afibrinogenemia

Blood, 2014-04, Vol.123 (14), p.2278-2281

2014

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MicroRNA-126 is a regulator of platelet-supported thrombin generation

Platelets (Edinburgh), 2020-08, Vol.31 (6), p.746-755

2020

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Fibrinogen Łódź: a new cause of dysfibrinogenemia associated with recurrent thromboembolic arterial events

Polskie archiwum medycyny wewne̦trznej, 2019-12, Vol.129 (12), p.934-935

2019

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A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype

Biomedicines, 2020-12, Vol.8 (12), p.605

2020

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Loss of Dicer in Sertoli Cells Has a Major Impact on the Testicular Proteome of Mice

Molecular & cellular proteomics, 2011-04, Vol.10 (4), p.M900587MCP200, Article M900587-MCP200

2011

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C2orf62 and TTC17 are involved in actin organization and ciliogenesis in zebrafish and human

PloS one, 2014-01, Vol.9 (1), p.e86476-e86476

2014

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Haematologic data, iron parameters and molecular findings in two new cases of iron-refractory iron deficiency anaemia

European journal of haematology, 2009-12, Vol.83 (6), p.595-602

2009

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DNA methylation profiling of the fibrinogen gene landscape in human cells and during mouse and zebrafish development

PloS one, 2013-08, Vol.8 (8), p.e73089

2013

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A liver enhancer in the fibrinogen gene cluster

Blood, 2011-01, Vol.117 (1), p.276-282

2011

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Physiological correction of hereditary mild hypofibrinogenemia during pregnancy

Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: A systematic literature review

A novel FGG missense variant associated with fibrinogen storage disease in a large family from Quebec

Hemizygous FGG p.Ala108Gly in a hypofibrinogenemic patient with a heterozygous 14.8 Mb deletion encompassing the entire fibrinogen gene cluster

Clinical Consequences and Molecular Bases of Low Fibrinogen Levels

Fibrin(ogen) in human disease: both friend and foe

Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations

Clinical Features and Management of Congenital Fibrinogen Deficiencies

Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders

Fibrinogen gene regulation

Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: case report and review of literature

Cryptic splice site usage leading to truncated TMPRSS6 is responsible for iron refractory iron deficiency anaemia in an Italian Family

Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders

Venous Thrombosis and Thrombocyte Activity in Zebrafish Models of Quantitative and Qualitative Fibrinogen Disorders

Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations

Targeted mutation of zebrafish fga models human congenital afibrinogenemia

MicroRNA-126 is a regulator of platelet-supported thrombin generation

Fibrinogen Łódź: a new cause of dysfibrinogenemia associated with recurrent thromboembolic arterial events

A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype

Loss of Dicer in Sertoli Cells Has a Major Impact on the Testicular Proteome of Mice

Inactivation of AMMECR1 is associated with growth, bone, and heart alterations

C2orf62 and TTC17 are involved in actin organization and ciliogenesis in zebrafish and human

Haematologic data, iron parameters and molecular findings in two new cases of iron-refractory iron deficiency anaemia

DNA methylation profiling of the fibrinogen gene landscape in human cells and during mouse and zebrafish development

A liver enhancer in the fibrinogen gene cluster

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