Diagnosis and treatment of a newborn with homozygous protein C deficiency
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.2004.tb00688.x/fullpdf
Reference14 articles.
1. Prevalence of protein C deficiency in the healthy population;Tait;Thromb Haemost,1995
2. Increased risk of venous thrombosis in carriers of hereditary protein C deficiency defect;Allaart;Lancet,1993
3. The human gene mutation database;Krawczak;Trends Genet,1997
4. Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies;Marlar;Semin Thromb Hemost,1990
5. Antepartum findings in fetal protein C deficiency;Kirkinen;Prenat Diagn,2000
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1. Case Report: Successful Long-Term Management of a Low-Birth Weight Preterm Infant With Compound Heterozygous Protein C Deficiency With Subcutaneous Protein C Concentrate Up to Adolescence;Frontiers in Pediatrics;2021-09-28
2. Use of hyperbaric oxygen therapy of purpura fulminans in an extremely low birth weight preterm: A case report;Journal of Neonatal-Perinatal Medicine;2020-07-29
3. The Newborn with Hematologic Abnormalities;Neonatology;2020-01-24
4. Early antithrombotic treatment with warfarin oral suspension in severe neonatal protein C deficiency;Archives de Pédiatrie;2017-04
5. Efficacy and safety of protein C concentrate to treat purpura fulminans and thromboembolic events in severe congenital protein C deficiency;Thrombosis and Haemostasis;2016-01
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