Results 141 to 150 of about 36,976 (279)
Beta O-39 thalassemia gene: a premature termination codon causes beta- mRNA deficiency without affecting cytoplasmic beta-mRNA stability [PDF]
R. Keith Humphries+4 more
openalex +1 more source
Pre-Natal Diagnosis of beta – Thalassemia by Chorionic Villous Sampling
Background: To promote the utility of Chorionic Villous Sampling (CVS) for pre-natal diagnosis of beta thalassemia in at risk population and to highlight its demographic area distribution and effect of consanguinity.
Shazia Syed,
doaj
Arthritis in beta‐thalassemia minor [PDF]
Pedro Fernández Del Vallado+3 more
openaire +3 more sources
Assessment of Iron Overload in Homozygous and Heterozygous Beta Thalassemic Children below 5 Years of Age [PDF]
Background: Thalassemia is a genetic disease having 3-7% carrier rate in Indians. It is transfusion dependent anemia having high risk of iron overloading.
Aparna Sagare, Dhiraj J. Trivedi
core
Therapeutic Value of Silymarin as Iron Chelator in Children with Beta Thalassemia with Iron Overload
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
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]
CD Boehm+4 more
openalex +1 more source
Molecular analysis of beta zero-thalassemia intermedia in Sardinia [PDF]
R Galanello+9 more
openalex +1 more source
OBJECTIVE: To determine the frequency of beta thalassemia trait in pregnant anemic patients attending Khyber Teaching Hospital, Peshawar, Pakistan. METHODS: This descriptive cross sectional study was conducted in Gynecology and Obstetrics Department of ...
Maimoona Qadir, Sohail Amir
doaj