Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian family [published erratum appears in Blood 1986 Jul;68(1):323] [PDF]
, 1986 CD Boehm +4 more
openalex +1 more source
eJHaem, Volume 6, Issue 4, August 2025.ABSTRACT Introduction Despite recent advances in sickle cell disease (SCD) research and management, there remains very limited information available on critically ill SCD patients requiring intensive care units (ICUs). Methods The National Inpatient Sample was queried using the International Classification of Diseases codes to identify critically ill ...
Tochukwu Nzeako +5 more
wiley +1 more source
Therapeutic Value of Silymarin as Iron Chelator in Children with Beta Thalassemia with Iron Overload
Mediterranean Journal of Hematology and Infectious Diseases, 2014 Beta thalassemia is an inherited hemoglobin disorder resulting in chronic hemolytic anemia. The most common treatment for thalassemia is blood transfusion which is necessary to provide the patients with healthy red blood cells containing normal ...
adel abd elhaleim hagag
doaj
The inactive beta globin gene on a gamma delta beta thalassemia chromosome has a normal structure and functions normally in vitro [PDF]
, 1988 PT Curtin, YW Kan
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Pediatric Blood &Cancer, Volume 72, Issue 8, August 2025.ABSTRACT Background Patients with sickle cell disease (SCD) experience painful vaso‐occlusive episodes that increase with age; a subset develops chronic pain (CP). CP is usually managed with acute pain management guidelines despite evidence of ineffectiveness.
Ashwin Patel +6 more
wiley +1 more source
Beta O-39 thalassemia gene: a premature termination codon causes beta- mRNA deficiency without affecting cytoplasmic beta-mRNA stability [PDF]
, 1984 R. Keith Humphries +4 more
openalex +1 more source
Hemoglobin F and Beta Thalassemia [PDF]
Science, 1967 Thomas G. Gabuzda +4 more
openaire +3 more sources
Clinical and Translational Science, Volume 18, Issue 8, August 2025.ABSTRACT Pharmacogenomics (PGx) can potentially tailor medication prescriptions to the genetic profiles of individuals, enhancing treatment outcomes and minimizing adverse drug reactions. This study assessed cardiovascular disease (CVD) patients' knowledge and views toward PGx testing in the United Arab Emirates (UAE).
Maram O. Abbas +11 more
wiley +1 more source
A novel beta-thalassemia frameshift mutation (codon 14/15), detectable by direct visualization of abnormal restriction fragment in amplified genomic DNA [PDF]
, 1988 Vivian Chan, TK Chan, YW Kan, D. Todd
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Economic burden of sickle cell disease in Australia
Internal Medicine Journal, Volume 55, Issue 8, Page 1251-1257, August 2025.Abstract Background Sickle cell disease (SCD) is an inherited condition that impairs red blood cell function, posing a substantial health burden on patients. As the prevalence of SCD in Australia rises due to migration, discussions surrounding treatment and management strategies are becoming more prominent. Aims Australia lacks a dedicated study on the
Steve Nwokeocha +32 more
wiley +1 more source