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1. A Case of a Pediatric Patient With Protein S Heerlen Polymorphism and Deep Venous Thrombosis.
2. Similar hypercoagulable state and thrombosis risk in type I and type III protein S-deficient individuals from mixed type I/III families.
3. [PROSI Mutation With Clinical Heterogeneity in Protein S Deficiency:Report of One Case].
4. First report of inherited protein S deficiency caused by paternal <i>PROS1</i> mosaicism.
5. Recommendations for clinical laboratory testing for protein S deficiency: Communication from the SSC committee plasma coagulation inhibitors of the ISTH.
6. Clinical characteristics, genes identification and follow-up study of a patient with central venous thrombosis from a protein S deficiency pedigree.
7. PROS1 variant c.1574C>T p.Ala525Val causes portal vein thrombosis with protein S deficiency.
8. Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiency.
9. Protein S levels and the risk of venous thrombosis: results from the MEGA case-control study.
10. Ischemic Stroke with Protein S Deficiency Treated by Apixaban.