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Papers of the Week

Home / Publications / Pain Research Forum / Papers of the Week / Clinical characteristics, genes identification and follow-up study of a patient with central venous thrombosis from a protein S deficiency pedigree.

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2021 Jan


Eur Rev Med Pharmacol Sci


http://www.ncbi.nlm.nih.gov/pubmed/33506924?dopt=Abstract


25


1

Clinical characteristics, genes identification and follow-up study of a patient with central venous thrombosis from a protein S deficiency pedigree.

Authors

Clinical characteristics, genes identification and follow-up study of a patient with central venous thrombosis from a protein S deficiency pedigree.
Wang T, Zhao X-J, Zhu H-D, Lu M, Wen B, Ma L
Eur Rev Med Pharmacol Sci. 2021 Jan; 25(1):353-361.
PMID: 33506924.

Abstract

To explore the clinical and prognostic features of CVT caused by PROS1 gene mutations and to provide clinical experience for new oral anticoagulants, such as rivaroxaban, in the treatment of CVT with a high risk of thrombosis.
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