Vasculopathy in Sickle Cell Disease: From Red Blood Cell Sickling to Vascular Dysfunction
Author:
Publisher
Wiley
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cphy.c200024
Reference185 articles.
1. Prevention of a First Stroke by Transfusions in Children with Sickle Cell Anemia and Abnormal Results on Transcranial Doppler Ultrasonography
2. Sickle cell vaso-occlusive crisis induces the release of circulating serum heat shock protein-70
3. Association between plasma free haem and incidence of vaso-occlusive episodes and acute chest syndrome in children with sickle cell disease
4. Automated RBC Exchange has a greater effect on whole blood viscosity than manual whole blood exchange in adult patients with sickle cell disease
5. Endothelial function and arterial stiffness in sickle-thalassemia patients
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1. Plasma monomeric ApoA1 and high‐density lipoprotein bound ApoA1 are markedly decreased and associated with low levels of lipophilic antioxidants in sickle cell disease: A potential new pathway for therapy;European Journal of Haematology;2024-08-20
2. Exercise and training in sickle cell disease: Safety, potential benefits, and recommendations;American Journal of Hematology;2024-08-12
3. Sickle Cell Disease Related Vasculopathies and Early Evaluation in a Pediatric Population;In Vivo;2024
4. Sickle Cell Disease and Other Risk Factors for Pediatric Arterial Ischemic Stroke: A Systematic Review and Meta-Analysis;Annals of Child Neurology;2024-01-01
5. Pain Control for Sickle Cell Crisis, a Novel Approach? A Retrospective Study;Medicina;2023-12-18
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