Results 201 to 210 of about 920,848 (226)

Overcoming transfusion-refractory anemia: partial splenic embolization to facilitate orthopedic surgery in β-thalassemia. [PDF]

Ann Hematol
Ye QQ, Zhou XG, Yang G, Xie WT, Yu AY, Duan HZ.   +5 more
europepmc   +1 more source

Clinical and Hematological Characteristics of Vietnamese Heterozygous Hb Tak/β-Thalassemia Patients: A Four-Case Series. [PDF]

Mediterr J Hematol Infect Dis
Nguyen TC, Nguyen TTH, Phi TNA, Le XH, Vu DL, Nguyen ND.   +5 more
europepmc   +1 more source

Metabolomic Investigation of Myelodysplastic Syndromes, Multiple Myeloma, and Homozygous β-Thalassemia. [PDF]

Cells
Chatzikalil E, Bistas K, Kymioni V, Diamantopoulos PT, Solomou EE.   +4 more
europepmc   +1 more source

Clinical integration of red cell genotyping in children with β-thalassemia major: a prospective observational study. [PDF]

Blood Glob Hematol
Gokcebay DG, Flegel WA.
europepmc   +1 more source

Red blood cell alloimmunization in transfusion-dependent β-thalassemia major patients in Eastern Iran. [PDF]

Ann Hematol
Shamahmood MN, Meghdadi MR, Nasiri M, Yousefi MJ, Mezginejad F.   +4 more
europepmc   +1 more source

β-Thalassemia

Genetics in Medicine, 2017
β-Thalassemia is caused by reduced (β +) or absent (β 0) synthesis of the β-globin chains of hemoglobin. Three clinical and hematological conditions of increasing severity are recognized: the β-thalassemia carrier state, thalassemia intermedia, and ...
Raffaella Origa
exaly   +2 more sources

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Rapid and simultaneous detection of β- thalassemia point mutations by reverse hybridization strip assay among Egyptian patients

Journal of Biochemistry, Microbiology and Biotechnology, 2016
Thalassemia is a wide range hereditary disease with high incidence in Egypt along with the high frequency of consanguineous marriages. Investigation the heterogeneity, molecular basis, and natural history are the most effective methods to deal with the thalassemia to develop effective method for management and prevention including the prenatal ...
Osama Shalaan, Moustafa Sakr, Ahmed Daif, Khalil Elhalfawy   +3 more
openaire   +1 more source

Clinical Classification, Screening and Diagnosis for Thalassemia

Hematology/Oncology Clinics of North America, 2018
Chayamon Takpradit, Supachai Ekwattanakit   +1 more
exaly  

Concomitant inheritance of α-thalassemia in β°-thalassemia/hb e disease

American Journal of Hematology, 1985
Suthat Fucharoen, P Winichagoon, P Wasi   +2 more
exaly  

Iron-Chelating Therapy and the Treatment of Thalassemia

Blood, 1997
Nancy Olivieri
exaly