Literature DB >> 18393984

Congenital hypofibrinogenemia associated with novel heterozygous fibrinogen Bbeta and gamma chain mutations.

G Castaman, S H Giacomelli, S Duga, F Rodeghiero.   

Abstract

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Year:  2008        PMID： 18393984     DOI： 10.1111/j.1365-2516.2008.01692.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN： 1351-8216            Impact factor:   4.287


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  4 in total

1.  Two novel fibrinogen variants in the C-terminus of the Bβ-chain: fibrinogen Rokycany and fibrinogen Znojmo.

Authors:  Roman Kotlín; Zuzana Reicheltová; Jirí Suttnar; Peter Salaj; Ingrid Hrachovinová; Tomás Riedel; Martin Malý; Milan Oravec; Jan Kvasnicka; Jan Evangelista Dyr
Journal:  J Thromb Thrombolysis       Date:  2010-10       Impact factor: 2.300

2.  Congenital fibrinogen disorders with repeated thrombosis.

Authors:  Xiuli Zhang; Chuang Zhang; Baoheng Wang; Ningheng Chen; Gaihe Sun; Xueli Guo
Journal:  J Thromb Thrombolysis       Date:  2020-02       Impact factor: 2.300

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

Authors:  Tomas Simurda; Jana Zolkova; Zuzana Snahnicanova; Dusan Loderer; Ingrid Skornova; Juraj Sokol; Jan Hudecek; Jan Stasko; Zora Lasabova; Peter Kubisz
Journal:  Int J Mol Sci       Date:  2017-12-29       Impact factor: 5.923

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

Authors:  Tomas Simurda; Rui Vilar; Jana Zolkova; Eliska Ceznerova; Zuzana Kolkova; Dusan Loderer; Marguerite Neerman-Arbez; Alessandro Casini; Monika Brunclikova; Ingrid Skornova; Miroslava Dobrotova; Marian Grendar; Jan Stasko; Peter Kubisz
Journal:  Biomedicines       Date:  2020-12-13
  4 in total

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