A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α 2 -antiplasmin) deficiency in an Italian patient-Reference-Cited by-同舟云学术

A novel allele variant of the SERPINF2 gene responsible for severe plasmin inhibitor (α 2 -antiplasmin) deficiency in an Italian patient

Published:2018-06 Issue: Volume:166 Page:60-62
ISSN:0049-3848
Container-title:Thrombosis Research
language:en
Short-container-title:Thrombosis Research

Author:

Viganò Silvana,D'Andrea Giovanna,Valle Patrizia Della,Santacroce Rosa,Margaglione Maurizio,D'Angelo Armando

Publisher

Elsevier BV

Subject

Hematology

Reference19 articles.

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3. α2-Antiplasmin and its deficiency: fibrinolysis out of balance;Carpenter;Haemophilia,2008

4. Meijer P, Hanss M, Christensen U, Wilman B, Kluft K. Criteria for the specific measurement of Plasmin Inhibitor activity using an enzymatic procedure. eJIFCC 13 2: http://www.ifcc.org/ejifcc/vol13no2/1301200107.htm

5. Mutation analysis in hyperphenylalaninemia patients from South Italy;Trunzo;Clin. Biochem.,2013

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1. Alpha2-Antiplasmin: The Devil You Don't Know in Cerebrovascular and Cardiovascular Disease;Frontiers in Cardiovascular Medicine;2020-12-23

2. Plasmin inhibitor deficiency: A case report;Clinical Case Reports;2020-01-07

3. Congenital Alpha-2 Antiplasmin Deficiency: a Literature Survey and Analysis of 123 Cases;Clinical Laboratory;2020

4. Hereditary angioedema: Looking for bradykinin production and triggers of vascular permeability;Clinical & Experimental Allergy;2019-10-21

5. A rare cause of bleeding in two Indian families with congenital alpha‐2‐antiplasmin deficiency;Haemophilia;2019-10-02