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

Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia

(2017) A. Casini et al.   HAEMOPHILIA

Thrombosis in Inherited Fibrinogen Disorders

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

Diagnosis and Treatment of von Willebrand Disease and Rare Bleeding Disorders

(2017) Giancarlo Castaman et al.   Journal of Clinical Medicine

Management of congenital quantitative fibrinogen disorders: a Delphi consensus

(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

Rare bleeding disorders: diagnosis and treatment

(2015) R. Palla et al.   BLOOD

Yes or no for secondary prophylaxis in afibrinogenemia?

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

Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families

(2015) A. Mukaddam et al.   HAEMOPHILIA

Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management

(2015) A. Casini 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

Comparison of predicted and actual consequences of missense mutations

(2015) Lisa A. Miosge et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

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

(2015) Rosanna Asselta et al.   THROMBOSIS AND HAEMOSTASIS

Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutations

(2015) Giancarlo Castaman et al.   THROMBOSIS RESEARCH

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

Novel homozygous fibrinogen Aα chain truncation causes severe afibrinogenemia with life threatening complications in a two-year-old boy

(2013) Jana Štikarová et al.   THROMBOSIS RESEARCH

A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia

(2012) Rita Marchi et al.   BLOOD CELLS MOLECULES AND DISEASES

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

(2011) E. GRANDONE et al.   HAEMOPHILIA

Regulation of fibrinogen production by microRNAs

(2010) A. Fort et al.   BLOOD

Congenital Fibrinogen Disorders

(2009) Philippe de Moerloose et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Congenital hypofibrinogenemia: Characterization of two missense mutations affecting fibrinogen assembly and secretion

(2008) Manuela Platè et al.   BLOOD CELLS MOLECULES AND DISEASES

Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bβ and γ chain mutations

(2008) G. CASTAMAN et al.   HAEMOPHILIA

Recommendations for nomenclature on fibrinogen and fibrin

(2008) L. MEDVED et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS