Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype

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

(2020) Rui Vilar et al.   HAEMATOLOGICA

Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia

(2020) Tomas Simurda et al.   INTERNATIONAL JOURNAL OF HEMATOLOGY

Perioperative management of a severe congenital hypofibrinogenemia with thrombotic phenotype

(2020) Tomas Simurda et al.   THROMBOSIS RESEARCH

Congenital hypofibrinogenemia associated with a novel heterozygous nonsense mutation in the globular C-terminal domain of the γ-chain (p.Glu275Stop)

(2019) Tomas Simurda et al.   JOURNAL OF THROMBOSIS AND THROMBOLYSIS

Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders

(2018) Giovanni Tiscia et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Clinical Consequences and Molecular Bases of Low Fibrinogen Levels

(2018) Marguerite Neerman-Arbez et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH

(2018) A Casini et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Mutational Epidemiology of Congenital Fibrinogen Disorders

(2018) Marc Blondon et al.   THROMBOSIS AND HAEMOSTASIS

Thromboelastography and Thromboelastometry in Assessment of Fibrinogen Deficiency and Prediction for Transfusion Requirement: A Descriptive Review

(2018) Henry T. Peng et al.   Biomed Research International

Fibrinogen as a Pleiotropic Protein Causing Human Diseases: The Mutational Burden of Aα, Bβ, and γ Chains

(2017) Elvezia Paraboschi et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders

(2017) Tomas Simurda et al.   INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES

Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation

(2017) A. Casini et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Thrombosis in Inherited Fibrinogen Disorders

(2017) Wolfgang Korte et al.   TRANSFUSION MEDICINE AND HEMOTHERAPY

Can the phenotype of inherited fibrinogen disorders be predicted?

(2016) A. Casini et al.   HAEMOPHILIA

Perioperative Coagulation Management in a Patient with Congenital Afibrinogenemia during Revision Total Hip Arthroplasty

(2016) Peter Kubisz et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia

(2016) Zuzana Snahnicanova et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders

(2016) Philippe de Moerloose et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Clinical Features and Management of Congenital Fibrinogen Deficiencies

(2016) Philippe de Moerloose et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Congenital afibrinogenemia: from etiopathogenesis to challenging clinical management

(2016) Lucia Stanciakova et al.   Expert Review of Hematology

Paradoxical Bleeding and Thrombosis in a Patient With Afibrinogenemia and Fibrinogen Mumbai Mutation

(2015) Alfiya Mukaddam et al.   AMERICAN JOURNAL OF CLINICAL PATHOLOGY

Not fibrin(ogen), but fibrinogen or fibrin

(2015) R. I. Litvinov et al.   BLOOD

Rare bleeding disorders: diagnosis and treatment

(2015) R. Palla et al.   BLOOD

Umbilical bleeding

(2015) Hassan Abolghasemi et al.   BLOOD COAGULATION & FIBRINOLYSIS

A case of congenital afibrinogenemia complicated with thromboembolic events that required repeated amputations

(2015) Mehmet A. Ozdemir et al.   BLOOD COAGULATION & FIBRINOLYSIS

Yes or no for secondary prophylaxis in afibrinogenemia?

(2015) Tomas Simurda et al.   BLOOD COAGULATION & FIBRINOLYSIS

Fibrinogen, red blood cells, and factor XIII in venous thrombosis

(2015) B. L. Walton et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module

(2015) R. Asselta et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Thromboembolic events in patients with severe inherited fibrinogen deficiency

(2015) Amihai Rottenstreich et al.   JOURNAL OF THROMBOSIS AND THROMBOLYSIS

Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency

(2015) Rosanna Asselta et al.   THROMBOSIS AND HAEMOSTASIS

Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylation

(2015) Rosanna Asselta et al.   THROMBOSIS RESEARCH

Fibrinogen-Related Proteins in Tissue Repair: How a Unique Domain with a Common Structure Controls Diverse Aspects of Wound Healing

(2015) Lorena Zuliani-Alvarez et al.   Advances in Wound Care

Natural history of patients with congenital dysfibrinogenemia

(2014) A. Casini et al.   BLOOD

Spontaneous epidural and subdural hematoma in a child with afibrinogenemia and postoperative management

(2014) Asiyan Kilit Y. et al.   BLOOD COAGULATION & FIBRINOLYSIS

Guideline for the diagnosis and management of the rare coagulation disorders

(2014) Andrew D. Mumford et al.   BRITISH JOURNAL OF HAEMATOLOGY

FGB mutations leading to congenital quantitative fibrinogen deficiencies: An update and report of four novel mutations

(2014) A. Casini et al.   THROMBOSIS RESEARCH

Fibrin(ogen) and thrombotic disease

(2013) R. A. S. Ariëns   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Mechanisms of Fibrinogen Adsorption at Solid Substrates at Lower pH

(2013) Michał Cieśla et al.   LANGMUIR

Congenital Fibrinogen Disorders: An Update

(2013) Alessandro Casini et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Occurrence of Thrombosis in Rare Bleeding Disorders

(2013) Arlette Ruiz-Saez   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders

(2012) F. PEYVANDI et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Mechanisms of Platelet Activation and Integrin αIIβ3

(2012) Seung-Jae Joo   Korean Circulation Journal

A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family

(2011) Emmanuel Levrat et al.   BLOOD COAGULATION & FIBRINOLYSIS

Clinical histories and molecular characterization of two afibrinogenemic patients: insights into clinical management

(2011) E. GRANDONE et al.   HAEMOPHILIA

Fibrinogen replacement therapy for congenital fibrinogen deficiency

(2011) L. BORNIKOVA et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Fibrinopeptides A and B release in the process of surface fibrin formation

(2010) T. Riedel et al.   BLOOD

Rare inherited disorders of fibrinogen

(2010) S. S. ACHARYA et al.   HAEMOPHILIA

Fibrinogen and the Risk of Thrombosis

(2010) Philippe de Moerloose et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Crystal Structure of Human Fibrinogen

(2009) Justin M. Kollman et al.   BIOCHEMISTRY

Rotational thromboelastography for monitoring of fibrinogen concentrate therapy in fibrinogen deficiency

(2008) Uwe Kalina et al.   BLOOD COAGULATION & FIBRINOLYSIS