Results 211 to 220 of about 3,873 (265)
Iron Overload, Clonal Hematopoiesis, and Cancer Risk in Aging and Transfusion-Dependent Populations: A Literature Review. [PDF]
CureusLa QD +11 more
europepmc +1 more source
High prevalence of Hb Q-Thailand not in cis with the -α<sup>4.2</sup> deletion: genotypes, phenotypes, and implications in the cenxi population of southern China. [PDF]
Front GenetLi Y, Wu M, Zheng L, Liang L, Li Y.
europepmc +1 more source
New England Journal of Medicine, 2014 More than 100 varieties of α-thalassemia have been identified. Their geographic distribution and the challenges associated with screening, diagnosis, and management suggest that α-thalassemias should have a higher priority on global public health ...
Frédéric B Piel, David J Weatherall
exaly +2 more sources
Progress Toward the Control and Management of the Thalassemias [PDF]
Hematology/Oncology Clinics of North America, 2016 Because of the particular high frequency of different severe forms of both and thalassemia in Asia the development of approaches for their prevention and management is particularly challenging.
Suthat Fucharoen, David J Weatherall
exaly +2 more sources
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Hemoglobin, 2022
Management and control of hemoglobinopathies are a challenge in India where 67.0% of people reside in rural regions. The GDP spent on health is one of the lowest (1.3%) resulting in high out-of-pocket expenses. The β-thalassemias are prevalent with an estimated 7500-12000 new births each year. Hb S (HBB: c.20A>T) and Hb E (HBB: c.79G>A) are also common
Roshan B, Colah, Tulika, Seth
openaire +2 more sources
Management and control of hemoglobinopathies are a challenge in India where 67.0% of people reside in rural regions. The GDP spent on health is one of the lowest (1.3%) resulting in high out-of-pocket expenses. The β-thalassemias are prevalent with an estimated 7500-12000 new births each year. Hb S (HBB: c.20A>T) and Hb E (HBB: c.79G>A) are also common
Roshan B, Colah, Tulika, Seth
openaire +2 more sources
Hematology, 2004
Abstract New developments in the epidemiology, treatment and prognosis of thalassemia have dramatically altered the approach to the care of affected patients, and these developments are likely to have an even greater impact in the next few years.
Alan R, Cohen +4 more
openaire +2 more sources
Abstract New developments in the epidemiology, treatment and prognosis of thalassemia have dramatically altered the approach to the care of affected patients, and these developments are likely to have an even greater impact in the next few years.
Alan R, Cohen +4 more
openaire +2 more sources