The Role of Inflammation in The Cellular and Molecular Mechanisms of Cardiopulmonary Complications of Sickle Cell Disease
Author:
Affiliation:
1. Department of Neurology and Rehabilitation Medicine, University of Cincinnati, Cincinnati, OH 45267-0525, USA
2. Division of Hematology & Oncology, Department of Internal Medicine, 3125 Eden Avenue, ML 0562, Cincinnati, OH 45219-0562, USA
Abstract
Funder
American Society of Hematology Scholar Award
Parker B. Francis Fellowship in Pulmonary Research Award
National Institutes of Health
Publisher
MDPI AG
Subject
Molecular Biology,Biochemistry
Link
https://www.mdpi.com/2218-273X/13/2/381/pdf
Reference147 articles.
1. Piel, F., Hay, S., Gupta, S., Weatherall, D., and Williams, T. (2013). Global burden of sickle cell anaemia in children under five, 2010-2050: Modelling based on demographics, excess mortality, and interventions. PLoS Med., 10.
2. Global epidemiology of sickle haemoglobin in neonates: A contemporary geostatistical model-based map and population estimates;Piel;Lancet,2013
3. Cardiopulmonary complications leading to premature deaths in adult patients with sickle cell disease;Fitzhugh;Am. J. Hematol.,2010
4. Cardiovascular complications and risk of death in sickle-cell disease;Gladwin;Lancet,2016
5. Cardiovascular complications of sickle cell disease;Sachdev;Trends Cardiovasc. Med.,2020
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