Results 81 to 90 of about 8,109 (242)
Anaemia Among Mother–Child Dyads in India: Trends, Drivers, and Future Projections
ABSTRACT Anaemia among mothers and their children is a widespread public health challenge with profound consequences for individuals and societies. While anaemia has been studied separately in women and children, there remains a literature gap examining anaemia in mother‐child dyads, limiting insights on interventions that may simultaneously address ...
Sarang Pedgaonker +8 more
wiley +1 more source
Abstract Background Acute pain transfusion reaction (APTR) is a rare, under‐recognized condition of unknown etiology. It can cause significant distress in recipients, necessitating symptomatic management and, occasionally, hospitalization. Study Design and Methods Here, we present an APTR event in an adult subject with transfusion‐dependent thalassemia
Georgia Tzafa +20 more
wiley +1 more source
Markers of coagulation activation in patients with hemoglobinopathy in Western Saudi Arabia
Objective: This study aims to examine markers of coagulation activation and their possible clinical associations in sickle cell disease (SCD) and thalassemia.
Soheir Adam, Galila Zaher
core +1 more source
Background: Nearly 226 million carriers of thalassemias and abnormal hemoglobin are present worldwide according to the World Health Organization (WHO). The laboratory plays an important role in the investigation of the thalassemias and hemoglobinopathies.
R Jha
doaj +1 more source
Codocytosis in the Dog: 345 Cases (2020–2022)
ABSTRACT Introduction Codocytes, or target cells, are a morphologic variation of erythrocytes characterized by increased membrane surface area relative to volume. In dogs, codocytosis is frequently noted on blood smear evaluation, but its clinical significance remains poorly understood. Objectives To characterize the clinical conditions associated with
Sarena M. Krojanker +5 more
wiley +1 more source
Background and aims: Hemoglobinopathy associated with the HBB gene, with its two general subtypes as thalassemia and abnormal hemoglobin (Hb) variants, is one of the most prevalent hereditary Hb disorders worldwide.
Huizhen Yuan (5216810) +12 more
core +1 more source
BACKGROUND: Thalassemia is a hereditary hemoglobinopathy characterized by inadequate or absent globin synthesis. This study aims to assess the prevalence and incidence of chronic pain in individuals with thalassemia within our population and further ...
Adel F. Al-Marzouki +12 more
doaj +1 more source
Abstract Background and Objectives Bedside transfusion errors, especially positive patient identification (PPID), are a risk to patient safety. Bedside electronic transfusion checks (BETC), using barcode‐enabled personal digital assistants (PDAs), are recommended to improve safety and efficiency.
Florence Oyekan +14 more
wiley +1 more source
Seroprevalence of Hepatitis B, Hepatitis C and HIV in patients with hemoglobinopathy hatients [PDF]
Amaç: Talasemi ve orak hücreli anemi hastaları sık transfüzyon almaktadır. Hepatit B (HBV), hepatit C (HCV) ve insan immün yetmezlik virüsü (HIV) kanla geçmektedir.
Acıpayam, Can +3 more
core
Evaluation of four different HPLC devices for hemoglobinopathy screening
Objective: Hemoglobinopathies are a common public health problem in Turkey. In the screening of these disorders in population, cation-exchange high performance liquid chromatography (HPLC) is accepted as the gold standard method.
Kader, Saadet +7 more
core +1 more source

