Absence of beta mRNA in beta0-thalassemia in Kurdish Jews [PDF]
, 1978 Francesco Ramirez +5 more
openalex +1 more source
Hereditary persistence of fetal hemoglobin or (delta beta)o- thalassemia: three types observed in South-Chinese families [PDF]
, 1985 Y T Zeng +6 more
openalex +1 more source
beta zero thalassemia in Sardinia is caused by a nonsense mutation. [PDF]
, 1981 Richard F. Trecartin +7 more
openalex +1 more source
Third-degree heart block in thalassemia major: A case report [PDF]
, 2012 Background: First and second-degree heart blocks are partly common rhythm disorders in thalassemic patients but complete heart block is a very rare complication of iron overload cardiomyopathy.
Hosseini, S.M., Maleki, A.R., Nikyar, B.
core +1 more source
A Search for Beta Thalassemia Trait in India
Turkish Journal of Hematology, 2012 To the Editor, The beta-thalassemia trait (BTT)—or beta-thalassemia minor—is a heterozygous condition in which only a single beta-globin gene is affected. The estimated prevalence of BTT in different regions of India is reported to vary between 2.7% and 14.9% (mean: 4.5%) [1,2].
openaire +4 more sources
Hemoglobin Mississippi (beta 44ser----cys). Studies of the thalassemic phenotype in a mixed heterozygote with beta +-thalassemia. [PDF]
, 1987 Martin H. Steinberg +6 more
openalex +1 more source
An approximately 300 bp deletion involving part of the 5' beta-globin gene region is observed in members of a Turkish family with beta- thalassemia [PDF]
, 1987 JC Diaz-Chico +5 more
openalex +3 more sources
Health Care Challenges of Hereditary Common Hematological Disorders in Odisha, India [PDF]
, 2012 Medical Genetics over the past few decades have emerged as an important and powerful medical specialty with increasing appreciation of its role and function in the biomedical sciences.
Balgir, RS
core +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
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