Literature DB >> 26103879

Novel protein C gene mutation in a compound heterozygote resulting in catastrophic thrombosis in early adulthood: diagnosis and long-term treatment with subcutaneous protein C concentrate.

Jir P Boey1,2,3, Alexandra Jolley4, Catherine Nicholls4, Nancy Lerda4, Elizabeth Duncan5, Alexander Gallus6,7,5, David M Ross6,7,5, Magdalena Sobieraj-Teague6,5.   

Abstract

Entities:  

Keywords:  compound heterozygote; frameshift mutation; protein C deficiency; rivaroxaban; subcutaneous infusion

Mesh：

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Year:  2015        PMID： 26103879     DOI： 10.1111/bjh.13538

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  3 in total

1.  Simultaneous Left Ventricular and Deep Vein Thrombi Caused by Protein C Deficiency.

Authors:  Harufumi Maki; Motohiro Nishiyama; Motoaki Shirakawa
Journal:  Case Rep Med       Date:  2017-01-17

2.  Direct Oral Anticoagulants in Patients Affected by Major Congenital Thrombophilia.

Authors:  Alessandra Serrao; Benedetta Lucani; Davide Mansour; Antonietta Ferretti; Erminia Baldacci; Cristina Santoro; Robin Foà; Antonio Chistolini
Journal:  Mediterr J Hematol Infect Dis       Date:  2019-07-01       Impact factor: 2.576

3.  Direct Oral Anticoagulants in Patients With Inherited Thrombophilia and Venous Thromboembolism: A Prospective Cohort Study.

Authors:  Elena Campello; Luca Spiezia; Chiara Simion; Daniela Tormene; Giuseppe Camporese; Fabio Dalla Valle; Anna Poretto; Cristiana Bulato; Sabrina Gavasso; Claudia Maria Radu; Paolo Simioni
Journal:  J Am Heart Assoc       Date:  2020-11-23       Impact factor: 5.501
  3 in total

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