Complications associated with sickle cell trait: a brief narrative review

G Tsaras, A Owusu-Ansah, FO Boateng… - The American journal of …, 2009 - Elsevier
Sickle cell trait occurs in approximately 300 million people worldwide, with the highest
prevalence of approximately 30% to 40% in sub-Saharan Africa. Long considered a benign …

Donor‐variation effect on red blood cell storage lesion: A close relationship emerges

VL Tzounakas, AG Kriebardis… - PROTEOMICS …, 2016 - Wiley Online Library
Although the molecular pathways leading to the progressive deterioration of stored red
blood cells (RBC storage lesion) and the clinical relevance of storage‐induced changes …

Etavopivat, a pyruvate kinase activator in red blood cells, for the treatment of sickle cell disease

P Schroeder, K Fulzele, S Forsyth… - … of Pharmacology and …, 2022 - ASPET
Etavopivat is an investigational, oral, small molecule activator of erythrocyte pyruvate kinase
(PKR) in development for the treatment of sickle cell disease (SCD) and other …

Compositions for activating pyruvate kinase

X Zheng, N Green, G Gustafson, DR Lancia Jr… - US Patent …, 2019 - Google Patents
2008/0184495 Al 8/2008 Brun et al. 2010/0120863 AL 5/2010 Biftu et al. 2010/0144594 A1
6/2010 Zoller et al. 2010/0216774 Al 8/2010 Bender et al. 2010/0324030 A1 12/2010 Dale …

Blood donors with thalassemic trait, glucose-6-phosphate dehydrogenase deficiency trait, and sickle cell trait and their blood products: current status and future …

E Noulsri, S Lerdwana - Laboratory Medicine, 2023 - academic.oup.com
The use of blood products for different medical purposes has increased in recent years. To
meet increasing demand, some blood centers allow volunteer donors with thalassemic trait …

Red blood cells from donors with sickle cell trait: a safety issue for transfusion?

AK Ould Amar - Transfusion Medicine, 2006 - Wiley Online Library
summary Sickle cell trait (SCT) affects approximately 8% of the population in Martinique
(FWI) and about the same rate is found among the African Americans. In several regions of …

Use of cell salvage in patients with sickle cell trait

A Okunuga, VA Skelton - International journal of obstetric …, 2009 - obstetanesthesia.com
1. Tsen L C. The more the merrier: should anesthesiologists be present for multiple births?
Int J Obstet Anesth 2008; 17: 205–7. 2. Carvalho B, Saxena A, Butwick A, Macario A. Vaginal …

[HTML][HTML] Comparação de metodologia utilizada para a detecção de hemoglobina S (Hb S) em doadores de sangue

BCAB Prudêncio, DT Covas… - Revista Brasileira de …, 2000 - SciELO Brasil
O Brasil apresenta alta prevalência de hemoglobina S, com nítidas diferenças regionais
marcadas pelos processos de miscigenação da população. A presença desta hemoglobina …

[HTML][HTML] Assessment of leucoreduction of sickle cell trait blood: quality of the filtered product

KO Amar, O Bourdonné, S Bruneau, F Sellami… - Blood …, 2014 - ncbi.nlm.nih.gov
Background With the implementation of universal leucoreduction of blood components in
several industrialised countries, the problems associated with leucocyte filtration of sickle …

Elastic properties of stored red blood cells from sickle trait donor units

MM Brandão, STO Saad, CL Cezar, A Fontes… - Vox …, 2003 - Wiley Online Library
Background and Objectives Red blood cells (RBCs) from patients with sickle cell disease
present reduced deformability. The aim of this study was to analyse the elasticity of stored …