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

Human Fibrinogen: Molecular and Genetic Aspects of Congenital Disorders

(2018) Giovanni Tiscia 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

Severe Wound Healing Impairment in a Patient with Dysfibrinogenaemia

(2018) Lize van Vulpen et al.   THROMBOSIS AND HAEMOSTASIS

Mutational Epidemiology of Congenital Fibrinogen Disorders

(2018) Marc Blondon et al.   THROMBOSIS AND HAEMOSTASIS

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

A novel mutation in the fibrinogen Aα chain (Gly13Arg, fibrinogen Nanning) causes congenital dysfibrinogenemia associated with defective peptide A release

(2016) Jie Yan et al.   INTERNATIONAL JOURNAL OF HEMATOLOGY

Three cases of congenital dysfibrinogenemia in unrelated Chinese families

(2016) Meiling Luo et al.   MEDICINE

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

Dysfibrinogenemia: from molecular anomalies to clinical manifestations and management

(2015) A. Casini et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

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

Natural history of patients with congenital dysfibrinogenemia

(2014) A. Casini et al.   BLOOD

Mechanisms of fibrin polymerization and clinical implications

(2013) J. W. Weisel et al.   BLOOD

Fibrinogen Hangzhou: Congenital dysfibrinogenemia caused by the novel missense mutation in FGG (γ308Asn→Thr)

(2013) Zhaoping Liao et al.   CLINICA CHIMICA ACTA

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

Clinical phenotype, laboratory features and genotype of 35 patients with heritable dysfibrinogenaemia

(2012) Susan E. Shapiro et al.   BRITISH JOURNAL OF HAEMATOLOGY

ISTH/SSC bleeding assessment tool: a standardized questionnaire and a proposal for a new bleeding score for inherited bleeding disorders

(2010) F. RODEGHIERO et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Fibrinogen and the Risk of Thrombosis

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

Comparison of the fibrinogen Clauss assay and the fibrinogen PT derived method in patients with dysfibrinogenemia

(2010) W. Miesbach et al.   THROMBOSIS RESEARCH

Congenital dysfibrinogenemia Aα Gly13Glu associated with bleeding during pregnancy

(2010) Roman Kotlín et al.   THROMBOSIS RESEARCH

Treatment of patients with dysfibrinogenemia and a history of abortions during pregnancy

(2009) Wolfgang Miesbach et al.   BLOOD COAGULATION & FIBRINOLYSIS

Inherited dysfibrinogenemia: clinical phenotypes associated with five different fibrinogen structure defects

(2009) Wolfgang Miesbach et al.   BLOOD COAGULATION & FIBRINOLYSIS

Pregnancy and rare bleeding disorders

(2009) R. KADIR et al.   HAEMOPHILIA