Homozygous protein S deficiency in an infant with purpura fulminans
- 30 November 1990
- journal article
- case report
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 117 (5), 750-753
- https://doi.org/10.1016/s0022-3476(05)83335-9
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Neonatal purpura fulminans associated with homozygous protein S deficiencyThe Lancet, 1990
- Diagnosis and treatment of homozygous protein C deficiency: Report of the working party on homozygous protein C deficiency of the subcommittee on protein C and protein S, international committee on thrombosis and haemostasisThe Journal of Pediatrics, 1989
- Severe protein C deficiency in newborn infantsThe Journal of Pediatrics, 1988
- An abnormal plasma distribution of protein S occurs in functional protein S deficiencyBlood, 1986
- Biosynthesis and secretion of factor VII, protein C, protein S, and the Protein C inhibitor from a human hepatoma cell lineBlood, 1986
- Serial studies of protein C and its plasma inhibitor in patients with disseminated intravascular coagulationBlood, 1985
- Familial protein S deficiency is associated with recurrent thrombosis.JCI Insight, 1984
- Homozygous Protein C Deficiency Manifested by Massive Venous Thrombosis in the NewbornNew England Journal of Medicine, 1984
- INHERITED PROTEIN C DEFICIENCY AND COUMARIN-RESPONSIVE CHRONIC RELAPSING PURPURA FULMINANS IN A NEWBORN INFANTThe Lancet, 1983
- Deficiency of protein C in congenital thrombotic disease.JCI Insight, 1981