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 …
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 …
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 …
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 …
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 …
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
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 …
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 …
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 …
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
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 …
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 …
sickle cell disease (SCD) patients. Blood was collected from haemoglobin (Hb) A volunteers …