The association of sickle cell disorder with adverse outcomes in COVID‐19 patients: A meta‐analysis

T Liang, K Guo, P Ni, G Duan… - Journal of Medical …, 2023 - Wiley Online Library
The aim is to elucidate the relationship between sickle cell disorder and severe COVID‐19.
We systematically searched the required articles in three electronic databases, extracting …

The properties of red blood cells from patients heterozygous for HbS and HbC (HbSC genotype)

A Hannemann, E Weiss, DC Rees, S Dalibalta… - Anemia, 2011 - Wiley Online Library
Sickle cell disease (SCD) is one of the commonest severe inherited disorders, but specific
treatments are lacking and the pathophysiology remains unclear. Affected individuals …

Sickle cell dehydration: Pathophysiology and therapeutic applications

C Brugnara - Clinical hemorheology and microcirculation, 2018 - content.iospress.com
Cell dehydration is a distinguishing characteristic of sickle cell disease and an important
contributor to disease pathophysiology. Due to the unique dependence of Hb S …

Cohort study of adult patients with haemoglobin SC disease: clinical characteristics and predictors of mortality

SFM Gualandro, GHH Fonseca… - British journal of …, 2015 - Wiley Online Library
Haemoglobin (Hb) SC disease is the second most common subtype of sickle cell disease
and is potentially fatal. This study aimed to determine the clinical characteristics, outcome …

Dengue in hospitalized children with sickle cell disease: a retrospective cohort study in the French departments of America

N Elenga, D Celicourt, B Muanza, G Elana… - Journal of Infection and …, 2020 - Elsevier
Background To describe the characteristics of dengue in sickle cell children and try to
identify risk factors of severity. Methods In this retrospective study, we describe the evolution …

The conductance of red blood cells from sickle cell patients: ion selectivity and inhibitors

YL Ma, DC Rees, JS Gibson… - The Journal of …, 2012 - Wiley Online Library
Key points• The high cation permeability in red blood cells (RBCs) from patients with sickle
cell disease (SCD) is central to pathogenesis and includes a deoxygenation‐induced …

Clinical and hematological profile in a newborn cohort with hemoglobin SC

PV Rezende, MV Santos, GF Campos, LLM Vieira… - Jornal de …, 2018 - SciELO Brasil
Objectives: Hemoglobin SC is the second most common variant of sickle-cell disease
worldwide, after hemoglobin SS. The objectives of the study were to describe the clinical …

Identification of the Ca2+ entry pathway involved in deoxygenation-induced phosphatidylserine exposure in red blood cells from patients with sickle cell disease

UM Cytlak, A Hannemann, DC Rees… - Pflügers Archiv-European …, 2013 - Springer
Phosphatidylserine (PS) exposure in red blood cells (RBCs) from sickle cell disease (SCD)
patients is increased compared to levels in normal individuals and may participate in the …

[HTML][HTML] The clinical significance of K-Cl cotransport activity in red cells of patients with HbSC disease

DC Rees, SL Thein, A Osei, E Drasar, S Tewari… - …, 2015 - ncbi.nlm.nih.gov
HbSC disease is the second commonest form of sickle cell disease, with poorly understood
pathophysiology and few treatments. We studied the role of K-Cl cotransport activity in …

The effect of hemolysis on plasma oxidation and nitration in patients with sickle cell disease

A Kupesiz, G Celmeli, S Dogan, B Antmen… - Free Radical …, 2012 - Taylor & Francis
This study aimed to determine the effect of haemolysis on plasma oxidation and nitration in
sickle cell disease (SCD) patients. Blood was collected from haemoglobin (Hb) A volunteers …