Sickle cell disease (SCD) is a group of inherited autosomal recessive disorders, including
sickle cell anemia, sickle beta-thalassemia, and other hemoglobinopathies, which are …

Objectives: Identify the epidemiology of macrocytic anemia. Summarize the evaluation of a
patient with macrocytic anemia. Outline the treatment and management options available for …

In this accessible analysis, a philosopher and a science educator look at biological theory
and society through a synthesis of mechanistic and organicist points of view to best …

Background Coexistence of polymorphisms of methylenetetrahydrofolate reductase
(MTHFR) with sickle cell gene exerts synergistic effect on complications associated with …

Background: Sickle cell disease (SCD), sickle cell anemia (SCA), and sickle beta-
thalassemia (SBT) are due to a mutated gene of hemoglobin (Hb), which makes the red …

Background Sickle cell disease (SCD) refers to a group of genetic disorders characterized
by the presence of an abnormal haemoglobin molecule called haemoglobin S (HbS). When …

Objective: This study was designed to assess the clinical features and survival outcomes of
pediatric Germ cell tumors (GCTs) in our center. Materials and Methods: All newly …

Objective: To investigate the potential benefits of using supplements, such as folic acid,
vitamin E, and calcium, to improve certain hematological parameters and overall well-being …

Introdução: A anemia falciforme (AF) é uma doença autossômica recessiva causada por
uma mutação no gene da globina β, originando a hemoglobina S, que possui o formato de …

Aim: The present study observed the relationship between the methylenetetrahydrofolate
reductase genotypes and clinical outcome in children with sickle cell disorder. Methodology …