Shear dependent red blood cell adhesion in microscale flow
Non-adherence and deformability are the key intrinsic biomechanical features of the red
blood cell (RBC), which allow it to tightly squeeze and pass through even the narrowest of …
blood cell (RBC), which allow it to tightly squeeze and pass through even the narrowest of …
[HTML][HTML] Prevalence of anemia, iron-deficiency anemia, and associated factors among children aged 1–5 years in the rural, malaria-endemic setting of Popokabaka …
Iron deficiency (ID), the leading cause of anemia and the most common nutritional deficiency
globally, is not well reported among children in malaria-endemic settings, and little is known …
globally, is not well reported among children in malaria-endemic settings, and little is known …
Nutritional status of sickle cell patients: a literature review
M Hur, B Durojaye - 2023 - research-archive.org
Sickle cell disease (SCD) is a lethal, life-long condition characterized by a mutation in the
gene that codes for hemoglobin. To alleviate the pain experienced by sickle cell (SC) …
gene that codes for hemoglobin. To alleviate the pain experienced by sickle cell (SC) …
Double‐blind clinical trial of arginine supplementation in the treatment of adult patients with sickle cell anaemia
RMN Eleutério, FO Nascimento… - Advances in …, 2019 - Wiley Online Library
Background. Sickle cell anaemia (SCA) is the most prevalent monogenic disease in Brazil.
In SCA, haemoglobin S (HbS) is formed, which modifies red blood cell morphology …
In SCA, haemoglobin S (HbS) is formed, which modifies red blood cell morphology …
[HTML][HTML] Overview of the clinical manifestations of sickle cell disease
EP Vichinsky - UpToDate, Waltham, MA, 2014 - medilib.ir
INTRODUCTION—The sickle point mutation in the beta globin gene results in the production
of sickle hemoglobin, which is less soluble than normal fetal or adult hemoglobin. Sickle cell …
of sickle hemoglobin, which is less soluble than normal fetal or adult hemoglobin. Sickle cell …
Phytochemistry, Mineral Estimation, Nutritional, and the In Vitro Anti-Sickling Potentials of Oil Extracted from the Seeds of Mucuna Flagellipes
EU Ejiofor, AC Ako, MT Kube, EC Agwamba… - Journal of the Mexican …, 2024 - jmcs.org.mx
Sickle cell disease is an inherited blood disorder indicative of red blood cells becoming
sickle-shaped. The study investigated the in vitro anti-sickling potentials of the seed oil of M …
sickle-shaped. The study investigated the in vitro anti-sickling potentials of the seed oil of M …
[PDF][PDF] Haematological Profile of Children With Sickle Cell Anaemia in Steady State
Sickle cell anaemia (SCA) is an inherited, autosomal recessive condition that results from a
mutation in the β-globin gene. Vascular occlusion is the underlying mechanism behind a …
mutation in the β-globin gene. Vascular occlusion is the underlying mechanism behind a …
Micronutrient levels and haemato-biochemical status of patients with sickle cell anaemia at a tertiary hospital in Abakaliki, south-eastern Nigeria: a cross-sectional …
Introduction: nutritional status is an under-studied environmental factor that can impact the
phenotypic manifestations of patients with Sickle cell anaemia (SCA). This study aimed to …
phenotypic manifestations of patients with Sickle cell anaemia (SCA). This study aimed to …
[PDF][PDF] Sickle Cell Disease Complications and BMI Percentiles of Pediatric Patients
AA Alaka, AA Iyanda - Asian J. Med. Health, 2024 - researchgate.net
ABSTRACT BMI percentile is a good index of nutritional status among pediatric patients. Yet
there is a dearth of information about the relationship between this important anthropometric …
there is a dearth of information about the relationship between this important anthropometric …
The Roles of Acute and Chronic Marrow Dysfunctions in the Aetiology of Anaemia in Sickle Cell Disease: Pathogenesis and Management: Marrow dysfunction in SCD
S Ahmed, U Ibrahim - Orient Journal of Medicine, 2024 - orientjom.org.ng
Background: Majority of the literature regarding the pathophysiology of anaemia in sickle
cell disease (SCD) is focused on intravascular and extravascular red cell haemolysis with …
cell disease (SCD) is focused on intravascular and extravascular red cell haemolysis with …