Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH-Reference-Cited by-同舟云学术

Diagnosis and management of severe congenital protein C deficiency (SCPCD): Communication from the SSC of the ISTH

Published:2022-07 Issue:7 Volume:20 Page:1735-1743
ISSN:1538-7836
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:Journal of Thrombosis and Haemostasis

Author:

Minford Adrian^ORCID,Brandão Leonardo R.^ORCID,Othman Maha^ORCID,Male Christoph^ORCID,Abdul‐Kadir Rezan,Monagle Paul,Mumford Andrew D.^ORCID,Adcock Dorothy,Dahlbäck Björn^ORCID,Miljic Predrag,DeSancho Maria T.^ORCID,Teruya Jun^ORCID

Publisher

Elsevier BV

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jth.15732

Reference37 articles.

1. Protein C deficiency;Goldenberg;Haemophilia,2008

2. Laboratory testing issues for protein C, protein S, and antithrombin;Marlar;Int J Lab Hematol,2014

3. American society of hematology 2018 guidelines for management of venous thromboembolism: treatment of pediatric venous thromboembolism;Monagle;Blood Adv,2018

4. Efficacy and safety of protein C concentrate to treat purpura fulminans and thromboembolic events in severe congenital protein C deficiency;Manco‐Johnson;Thromb Haemost,2016

5. Treatment of inherited protein C deficiency by replacement therapy with the French purified plasma‐derived protein C concentrate (PROTEXEL);Dreyfus;Vox Sang,2007

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Real-world treatment of patients with severe congenital protein C deficiency with protein C concentrate: A physician survey;Thrombosis Update;2024-01

2. The clinical and genetic landscape of early‐onset thrombophilia in Japan;Pediatric Blood & Cancer;2023-12-28

3. Molecular basis of inherited protein C deficiency results from genetic variations in the signal peptide and propeptide regions;Journal of Thrombosis and Haemostasis;2023-11

4. Evaluation of living donors for hereditary liver disease (siblings, heterozygotes);Journal of Hepatology;2023-06

5. Cure of congenital purpura fulminans via expression of engineered protein C through neonatal genome editing in mice;2023-02-26