Results 111 to 120 of about 32,142 (226)
Rapid turnover of T cells in acute infectious mononucleosis.
During acute infectious mononucleosis (AIM), large clones of Epstein-Barr virus-specific T lymphocytes are produced. To investigate the dynamics of clonal expansion, we measured cell proliferation during AIM using deuterated glucose to label DNA of ...
Asquith, Becca +9 more
core +1 more source
HbA1c levels in hemoglobin H disease
Background: Patients with beta-thalassemia have been shown to exhibit lower HbA1c levels, often correlating with reduced hemoglobin (Hb) concentrations.
Pasiri Kerdsinchai +14 more
doaj +1 more source
Effect of booklet and combined method on parents' awareness of children with β-thalassemia major disorder [PDF]
OBJECTIVE: To assess the effects of booklet and combining methods (lecture, video, etc.) on parents' awareness of children with beta-thalassemia major disorder.
Hasanpour-Dehkordi, A. +1 more
core
LABRAD : Vol 40, Issue 1 - April 2014 [PDF]
Provocative Testing for Growth Hormone Disorders Serum Procalcitonin for Early Sepsis Diagnosis Monoclonal Gammopathy of Undetermined Significance (MGUS) Understanding Six Sigma Methodology Blood Collection for Culture Molecular Analysis of Alpha ...
Aga Khan University Hospital, Karachi
core +1 more source
Glioma through the looking GLASS: molecular evolution of diffuse gliomas and the Glioma Longitudinal Analysis Consortium. [PDF]
Adult diffuse gliomas are a diverse group of brain neoplasms that inflict a high emotional toll on patients and their families. The Cancer Genome Atlas and similar projects have provided a comprehensive understanding of the somatic alterations and ...
GLASS Consortium
core
Prevalence of common point mutations of alpha globin gene in Babol, Iran (2005-09)
Background and Objective: Alpha thalassemia is one of the most common hemoglobin disorders. Some combination of alpha globin gene mutations may cause HbH disease with severe anemia or intermediate thalassemia.
Akhavan-Niaki H (PhD) +4 more
doaj
BACKGROUND: Thalassemia, a hereditary blood disorder, poses a significant health challenge globally. This study delves into the prevalence and characteristics of thalassemia, emphasizing the need for enhanced awareness and diagnostic measures ...
Hussein Fadi Ibrahim +4 more
doaj +1 more source
Comparison of the HbH inclusion test and a PCR test in routine screening for α thalassaemia in Hong Kong [PDF]
Aim - To compare the haemoglobin (Hb) H inclusion test with a polymerase chain reaction CPCR) test in routine screening for or thalassaemia. Methods - Ninety nine peripheral blood samples from Chinese patients with mean corpuscular volume below 80fl were
Chan, AYY, Chan, LC, So, CKC
core
Frequency of alpha-thalassemia in Greece.
Using hematological and gene mapping techniques, a cord blood survey was carried out to estimate the frequency of alpha-thalassemia in the Greek population. Out of 227 newborns studied, 16 (7.05%) were found by gene mapping to be alpha-thalassemia 2 heterozygotes (-alpha/alpha alpha), and of these only two had increased levels of hemoglobin Bart's in ...
KANAVAKIS, E +4 more
openaire +2 more sources

