Filters

Yana N Kotova, Nadezhda A Podoplelova, Sergey I Obydennyy, Elizaveta A Kostanova, Alexander A Ryabykh, Aleksandra S Demyanova, Maria I Biriukova, Mark A Rosenfeld, Alexey V Sokolov, Herve Chambost, Maria A Kumskova, Fazoil I Ataullakhanov, Marie-Christine Alessi, Mikhail A Panteleev

Thrombosis and haemostasis 2019;119(6):906-915

Full Text

Abstract

A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream.

H Robert-Ebadi, P de Moerloose, M El Khorassani, M El Khattab, M Neerman-Arbez

Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2009;20(5):385-7

Full Text

Abstract

Rare coagulation disorders: fibrinogen, factor VII and factor XIII.

P de Moerloose, J-F Schved, D Nugent

Haemophilia : the official journal of the World Federation of Hemophilia 2017;22 Suppl 5():61-5

Full Text

Abstract

The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation.

P H B Bolton-Maggs, D J Perry, E A Chalmers, L A Parapia, J T Wilde, M D Williams, P W Collins, S Kitchen, G Dolan, A D Mumford

Haemophilia : the official journal of the World Federation of Hemophilia 2005;10(5):593-628

Full Text

Abstract

The molecular mechanisms of congenital hypofibrinogenaemia.

G J Maghzal, S O Brennan, V M Homer, P M George

Cellular and molecular life sciences : CMLS 2004;61(12):1427-38

Free Full Text

Abstract

Acute obstetric coagulopathy during postpartum hemorrhage is caused by hyperfibrinolysis and dysfibrinogenemia: an observational cohort study.

Lucy de Lloyd, Peter V Jenkins, Sarah F Bell, Nicola J Mutch, Julia Freyer Martins Pereira, Pilar M Badenes, Donna James, Anouk Ridgeway, Leon Cohen, Thomas Roberts, Victoria Field, Rachel E Collis, Peter W Collins

Journal of thrombosis and haemostasis : JTH 2023;21(4):862-879

Free Full Text

Abstract

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

A Casini, T Brungs, C Lavenu-Bombled, R Vilar, M Neerman-Arbez, P de Moerloose

Journal of thrombosis and haemostasis : JTH 2018;15(5):876-888

Free Full Text

Abstract

Successful intravenous thrombolysis for acute ischemic stroke caused by aortic dissection with severe hypofibrinogenemia: a case report and literature review.

Liming Cao, Xuming Huang, Fei-Qi Zui

The International journal of neuroscience 2022;132(9):939-944

Free Full Text

Abstract

Genetic and environmental determinants of fibrin structure and function: relevance to clinical disease.

Eleanor M Scott, Robert A S Ariëns, Peter J Grant

Arteriosclerosis, thrombosis, and vascular biology 2005;24(9):1558-66

Full Text

Abstract

Results: 1 – 15 / 16

Filters

Expert Opinion

Text Availability

Publication Types

Publication Year

Results for ""Afibrinogenemia""[mesh_terms]

Molecular mechanisms of hypo- and afibrinogenemia.

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

The amplitude of coagulation curves from thrombin time tests allows dysfibrinogenemia caused by the common mutation FGG-Arg301 to be distinguished from hypofibrinogenemia.

Abnormal fibrinogen with an Aα 16Arg → Cys substitution is associated with multiple cerebral infarctions.

Structural alterations in hereditary dysfibrinogens.

A novel fibrinogen γ chain frameshift deletion (c.637delT) in a patient with hypodysfibrinogenemia associated with thrombosis.

Binding of Coagulation Factor XIII Zymogen to Activated Platelet Subpopulations: Roles of Integrin αIIbβ3 and Fibrinogen.

A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream.

Rare coagulation disorders: fibrinogen, factor VII and factor XIII.

The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation.

The molecular mechanisms of congenital hypofibrinogenaemia.

Acute obstetric coagulopathy during postpartum hemorrhage is caused by hyperfibrinolysis and dysfibrinogenemia: an observational cohort study.

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

Successful intravenous thrombolysis for acute ischemic stroke caused by aortic dissection with severe hypofibrinogenemia: a case report and literature review.

Genetic and environmental determinants of fibrin structure and function: relevance to clinical disease.

Results for
""Afibrinogenemia""[mesh_terms]