Homozygous protein S deficiency in an infant with purpura fulminans
- 1 November 1990
- journal article
- case report
- Published by Elsevier 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 14 references indexed in Scilit:
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- Diagnosis and treatment of homozygous protein C deficiencyThe Journal of Pediatrics, 1989
- Severe protein C deficiency in newborn infantsThe Journal of Pediatrics, 1988
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- 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.Journal of Clinical Investigation, 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.Journal of Clinical Investigation, 1981