Literature DB >> 30076675

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

A Casini1, A Undas2, R Palla3, J Thachil4, P de Moerloose5.   

Abstract

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Year:  2018        PMID： 30076675     DOI： 10.1111/jth.14216

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN： 1538-7836            Impact factor:   5.824


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  22 in total

1.  Congenital dysfibrinogenaemia presented with preterm premature rupture of the membranes and vaginal bleeding.

Authors:  Zaker I Schwabkey; Farrell C Sheehan; Courtney Bellomo; Mihir Raval
Journal:  BMJ Case Rep       Date:  2020-09-18

Review 2.  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.

Authors:  Tomas Simurda; Monika Brunclikova; Rosanna Asselta; Sonia Caccia; Jana Zolkova; Zuzana Kolkova; Dusan Loderer; Ingrid Skornova; Jan Hudecek; Zora Lasabova; Jan Stasko; Peter Kubisz
Journal:  Int J Mol Sci       Date:  2020-06-29       Impact factor: 5.923

Review 3.  Fibrinogen and fibrin: An illustrated review.

Authors:  Marlien Pieters; Alisa S Wolberg
Journal:  Res Pract Thromb Haemost       Date:  2019-03-04

4.  Fibrinogen concentrate for bleeding in patients with congenital fibrinogen deficiency: Observational study of efficacy and safety for prophylaxis and treatment.

Authors:  Joseph Lasky; Jerome Teitel; Michael Wang; Danielle Dalton; Dirk Steffen Schmidt; Andres Brainsky
Journal:  Res Pract Thromb Haemost       Date:  2020-10-11

5.  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

6.  Whole Blood Thromboelastometry by ROTEM and Thrombin Generation by Genesia According to the Genotype and Clinical Phenotype in Congenital Fibrinogen Disorders.

Authors:  Timea Szanto; Riitta Lassila; Marja Lemponen; Elina Lehtinen; Marguerite Neerman-Arbez; Alessandro Casini
Journal:  Int J Mol Sci       Date:  2021-02-25       Impact factor: 5.923

7.  Efficacy and safety of fibrinogen concentrate for on-demand treatment of bleeding and surgical prophylaxis in paediatric patients with congenital fibrinogen deficiency.

Authors:  Claudia Djambas Khayat; Sunil Lohade; Fulton D'Souza; Latha Gowda Shamanur; Omid Reza Zekavat; Irina Kruzhkova; Bruce Schwartz; Cristina Solomon; Sigurd Knaub; Flora Peyvandi
Journal:  Haemophilia       Date:  2020-12-16       Impact factor: 4.287

8.  Hepatic fibrinogen storage disease and hypofibrinogenemia caused by fibrinogen Aguadilla mutation: a case report.

Authors:  Leilei Gu; Bin Wang; Lu Liu; Qiaorong Gan; Xiaolong Liu; Lihong Chen; Li Chen
Journal:  J Int Med Res       Date:  2020-01       Impact factor: 1.671

Review 9.  Fibrin(ogen) in human disease: both friend and foe.

Authors:  Rui Vilar; Richard J Fish; Alessandro Casini; Marguerite Neerman-Arbez
Journal:  Haematologica       Date:  2020-01-31       Impact factor: 9.941

10.  Pregnancy outcome in afibrinogenemia: Are we giving enough fibrinogen concentrate? A case series.

Authors:  Joline L Saes; Britta A P Laros-van Gorkom; Michiel Coppens; Saskia E M Schols
Journal:  Res Pract Thromb Haemost       Date:  2020-01-22
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