Diagnosis and classification of congenital fibrinogen disorders: communication from the SSC of the ISTH-Reference-Cited by-同舟云学术

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

Published:2018-08-03 Issue:9 Volume:16 Page:1887-1890
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Casini A.¹,Undas A.²,Palla R.³,Thachil J.⁴,de Moerloose P.⁵,

Affiliation:

1. Division of Angiology and Haemostasis; Faculty of Medicine; University Hospitals of Geneva; Geneva Switzerland

2. Institute of Cardiology; Jagiellonian University Medical College; John Paul II Hospital; Cracow Poland

3. Department of Medicine and Medical Specialities; Angelo Bianchi Bonomi Hemophilia and Thrombosis Center; University of Milan; IRCCS Maggiore Hospital; Milan Italy

4. Department of Haematology; Central Manchester University Hospitals NHS Foundation Trust; Manchester UK

5. Faculty of Medicine; University Hospitals of Geneva; Geneva Switzerland

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.14216/fullpdf

Reference25 articles.

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2. Fibrinogen as a pleiotropic protein causing human diseases: the mutational burden of aalpha, bbeta, and gamma chains;Paraboschi;Int J Mol Sci,2017

3. Laboratory and genetic investigation of mutations accounting for congenital fibrinogen disorders;Neerman-Arbez;Semin Thromb Hemost,2016

4. Hereditary renal amyloidosis associated with a mutant fibrinogen alpha-chain;Benson;Nat Genet,1993

5. Recommendations for nomenclature on fibrinogen and fibrin;Medved;J Thromb Haemost,2009

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