Sickle Cell Disease: Current Understanding and Future Options-Reference-Cited by-同舟云学术

Sickle Cell Disease: Current Understanding and Future Options

Published:2023-09-13 Issue:18 Volume:12 Page:5943
ISSN:2077-0383
Container-title:Journal of Clinical Medicine
language:en
Short-container-title:JCM

Author:

Varelas Christos¹^ORCID,Gavriilaki Eleni²^ORCID

Affiliation:

1. Hematology Department—BMT Unit, G .Papanicolaou Hospital, 57010 Thessaloniki, Greece

2. 2nd Propedeutic Department of Internal Medicine, Aristotle University of Thessaloniki, 54644 Thessaloniki, Greece

Abstract

Sickle cell disease (SCD) is a prevalent inherited hemoglobin disorder encompassing a cluster of congenital hemolytic anemias, each distinguished by the prevalence of sickle hemoglobin (HbS) [...]

Publisher

MDPI AG

Subject

General Medicine

Link

https://www.mdpi.com/2077-0383/12/18/5943/pdf

Reference9 articles.

1. Complement in Sickle Cell Disease: Are We Ready for Prime Time?;Varelas;J. Blood Med.,2021

2. Successful Outcome of Hyperhemolysis in Sickle Cell Disease following Multiple Lines of Treatment: The Role of Complement Inhibition;Vlachaki;Hemoglobin,2018

3. Successful Outcome of Chronic Intrahepatic Cholestasis in an Adult Patient with Sickle Cell/ beta+ Thalassemia;Vlachaki;Case Rep. Hematol.,2014

4. Complement in sickle cell disease and targeted therapy: I know one thing, that I know nothing;Tampaki;Blood Rev.,2021

5. Castonguay, M., Dakhallah, N., Desroches, J., Colaiacovo, M.L., Jimenez-Cortes, C., Claveau, A.M., Berube, S., Hafsaoui, A.Y., Souza, A., and Tibout, P. (2022). COVID-19 and Sickle Cell Disease in the Province of Quebec, Canada: Outcomes after Two Years of the Pandemic. J. Clin. Med., 11.

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