Hypoglycosylation is a common finding in antithrombin deficiency in the absence of aSERPINC1gene defect-Reference-Cited by-同舟云学术

Hypoglycosylation is a common finding in antithrombin deficiency in the absence of aSERPINC1gene defect

Published:2016-06-29 Issue:8 Volume:14 Page:1549-1560
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

de la Morena-Barrio M. E.¹²,Martínez-Martínez I.¹²,de Cos C.³,Wypasek E.⁴⁵,Roldán V.¹,Undas A.⁴⁵,van Scherpenzeel M.⁶,Lefeber D. J.⁶,Toderici M.¹,Sevivas T.⁷,España F.⁸,Jaeken J.⁹,Corral J.¹²,Vicente V.¹²

Affiliation:

1. Servicio de Hematología y Oncología Médica; Hospital Universitario Morales Meseguer; Centro Regional de Hemodonación; Universidad de Murcia; IMIB-Arrixaca; Murcia Spain

2. Grupo de investigación CB15/00055 del Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER); Instituto de Salud Carlos III (ISCIII); Madrid Spain

3. Hospital Puerta del Mar; Cádiz Spain

4. The John Paul II Hospital; Kraków Poland

5. Institute of Cardiology; Jagiellonian University Medical College; Kraków Poland

6. Department of Neurology; Laboratory for Genetic, Endocrine and Metabolic Diseases; Radboud University Medical Center; Nijmegen the Netherlands

7. Serviço de Hematologia do Centro Hospitalar e Universitário de Coimbra; Coimbra Portugal

8. Grupo de Hemostasiam Trombosis, Arteriosclerosis y Biología Vascular; Centro de Investigación; Hospital Universitario y Politécnico La Fe; Valencia Spain

9. Center for Metabolic Diseases; Universitair Ziekenhuis Gasthuisberg; Leuven Belgium

Funder

Instituto de Salud Carlos III

Fundación Española de Trombosis y Hemostasia

GATRA Grifols Award

Ministerio de Economia y Competitividad

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.13372/fullpdf

Reference45 articles.

1. Inherited antithrombin deficiency causing thrombophilia;Egeberg;Thromb Diath Haemorrh,1965

2. Inherited risk factors for venous thromboembolism;Martinelli;Nat Rev Cardiol,2014

3. Selective testing for thrombophilia in patients with first venous thrombosis: results from a retrospective family cohort study on absolute thrombotic risk for currently known thrombophilic defects in 2479 relatives;Lijfering;Blood,2009

4. A prospective cohort study on the absolute risks of venous thromboembolism and predictive value of screening asymptomatic relatives of patients with hereditary deficiencies of protein S, protein C or antithrombin;Mahmoodi;J Thromb Haemost,2010

5. Age- and gender-specific familial risks for venous thromboembolism: a nationwide epidemiological study based on hospitalizations in Sweden;Zoller;Circulation,2011

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