Diagnosis and management of neonatal purpura fulminans
- 31 December 2011
- journal article
- review article
- Published by Elsevier BV in Seminars in Fetal and Neonatal Medicine
- Vol. 16 (6), 318-322
- https://doi.org/10.1016/j.siny.2011.07.009
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- Human protein C concentrate in the treatment of purpura fulminans: a retrospective analysis of safety and outcome in 94 pediatric patientsCritical Care, 2010
- Purpura fulminans in a newborn infant with galactosemiaEuropean Journal of Pediatrics, 2009
- ProCMD: a database and 3D web resource for protein C mutantsBMC Bioinformatics, 2007
- Developmental haemostasisThrombosis and Haemostasis, 2006
- Severe Protein S Deficiency Associated with Heterozygous Factor V Leiden Mutation in a Child with Purpura FulminansPediatric Hematology and Oncology, 2003
- Severe neonatal protein C deficiency: Prevalence and thrombotic riskThe Journal of Pediatrics, 1991
- Homozygous protein S deficiency in an infant with purpura fulminansThe Journal of Pediatrics, 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
- Prenatal Diagnosis of Hereditary Protein C DeficiencyNew England Journal of Medicine, 1985
- Homozygous Protein C Deficiency Manifested by Massive Venous Thrombosis in the NewbornNew England Journal of Medicine, 1984