[HTML][HTML] Erythrocyte sedimentation rate

K Tishkowski, V Gupta - 2020 - europepmc.org
The erythrocyte sedimentation rate (sedimentation rate, sed rate, and ESR for short) is a
common hematology test that may indicate and monitor an increase in inflammatory activity …

The clinical utility of standard and high-sensitivity C-Reactive protein: a narrative review

FZ Rahali, N Mimouni, A Boukhira… - SN comprehensive clinical …, 2024 - Springer
C-reactive protein (CRP) is an acute phase protein predominantly produced in the liver and
regulated by pro-inflammatory cytokines. CRP belongs to the pentraxin family and is …

Sickle cell disease: Hemostatic and inflammatory changes, and their interrelation

SLO Toledo, JVM Guedes, PN Alpoim, DRA Rios… - Clinica Chimica …, 2019 - Elsevier
Sickle cell disease, the most common genetic blood disorder in the world, has high clinical
variability, negatively impacts quality of life and contributes to early mortality. Sickled …

Red blood cell adhesion to heme‐activated endothelial cells reflects clinical phenotype in sickle cell disease

E Kucukal, A Ilich, NS Key, JA Little… - American journal of …, 2018 - Wiley Online Library
In sickle cell disease (SCD),'disease severity'associates with increased RBC adhesion to
quiescent endothelium, but the impact on activated endothelium is not known. Increased …

Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profiles

MM Aleluia, TCC Fonseca, RQ Souza, FI Neves… - BMC hematology, 2017 - Springer
Background In this study, we evaluate the association of different clinical profiles, laboratory
and genetic biomarkers in patients with sickle cell anemia (SCA) and hemoglobin SC …

Immunological hallmarks of inflammatory status in vaso-occlusive crisis of sickle cell anemia patients

AL Silva-Junior, NP Garcia, EC Cardoso… - Frontiers in …, 2021 - frontiersin.org
Sickle Cell Anemia (SCA) is the most common genetic disorder around the world. The
mutation in the β-globin gene is responsible for a higher hemolysis rate, with further …

[HTML][HTML] The Role of erythrocyte sedimentation rate (ESR) in myeloproliferative and lymphoproliferative diseases: comparison between diesse cube 30 touch and …

M Pelagalli, F Tomassetti, E Nicolai, A Giovannelli… - Diseases, 2023 - mdpi.com
(1) Background: The erythrocyte sedimentation rate (ESR) is widely diffused in hematology
laboratories to monitor inflammatory statuses, response to therapies (such as antibiotics) …

Estimation of malondialdehyde levels in serum and saliva of children affected with sickle cell anemia

S Baliga, M Chaudhary, S Bhat… - Journal of Indian …, 2018 - journals.lww.com
Background: Sickle cell anemia (SCA) is an inherited disorder of hemoglobin synthesis
characterized by deformed erythrocytes. Hemoglobin S present in sickle-shaped …

Predicting risk factors for thromboembolic complications in patients with sickle cell anaemia–lessons learned for prophylaxis

S Alkindi, AR Al-Ghadani… - Journal of …, 2021 - journals.sagepub.com
Objective To assess the clinical and laboratory predictors of venous thromboembolism (VTE)
in patients with sickle cell anaemia (SCA) and its relationship to morbidity and mortality …

Current perspectives of sickle cell disease in Nigeria: changing the narratives

OO Ojewunmi, TA Adeyemo, OC Ayinde… - Expert Review of …, 2019 - Taylor & Francis
Introduction: Sickle cell disease (SCD) is an inherited blood disorder characterized by
clinical heterogeneity that may be influenced by environmental factors, ethnicity, race, social …