Results 271 to 280 of about 181,456 (327)

Bone Marrow Transplantation in Thalassemia (Part 1)

, 2009
Maryam Zakerinia
openalex   +1 more source

Prevalence of Alloantibodies in Transfusion-dependent Thalassemia Patients

Neha Parashar, Divya Gupta, Tanvi Bhardwaj, Sunil Kumar, Rashmi Jain Gupta, Sapna Erat Sreedharan   +5 more
openalex   +1 more source

Investigation on the Anxiety and Depression Status of Thalassemia Carriers After Genetic Counseling. [PDF]

Neuropsychiatr Dis Treat
Pan J, Xu A, Tung TH, Shen B.
europepmc   +1 more source

Accurate diagnosis of hemoglobinopathies with machine learning based on high-throughput proteomics. [PDF]

Hemasphere
Wei S, Nielsen AB, Helby J, Drici L, Rasmussen C, Wang J, Mann M, Petersen J, Wewer Albrechtsen NJ, Glenthøj A.   +9 more
europepmc   +1 more source

Frequency of Zinc Deficiency Among Thalassemia Major Patients: A Comparative Cross-Sectional Study. [PDF]

Cureus
Hayat U, Zaidi U, Munzir S, Dildar S, Sharif Z, Farzana T, Nizamuddin M, Shamsi T.   +7 more
europepmc   +1 more source

Assessment of β-Thalassemia Trait Occurrence in an Outpatient Sample from Southern Chile: A Retrospective Study. [PDF]

Diagnostics (Basel)
Balcázar-Villarroel M, Mancilla-Uribe A, Navia-León S, Carrasco-Fajardin L, Bohle-Matamala J, Calbucura-Ovalle C, Torrens F, Carmine-Peña E, Sandoval C, Peña F.   +9 more
europepmc   +1 more source

Epidemiological study of thalassemia in the Buyi population of Qiannan Prefecture, Guizhou Province, China based on third-generation sequencing. [PDF]

Ann Hematol
Wu J, Wang L, Jin Z, Ren L, Shi Y, Zhou Y, Meng G, Mao A, Cui D, An B, Huang S.   +10 more
europepmc   +1 more source

Beta-thalassemia [PDF]

Genetics in Medicine, 2010
Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis of the beta chains of hemoglobin resulting in variable phenotypes ranging from severe anemia to clinically asymptomatic individuals. The total annual incidence of symptomatic individuals is estimated at 1 in 100,000 throughout the world and 1 in 10 ...
Galanello R, ORIGA, RAFFAELLA
exaly   +8 more sources

β-Thalassemia [PDF]

Genetics in Medicine, 2017
β-Thalassemia is caused by reduced (β+) or absent (β0) 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 thalassemia major, a severe transfusion-dependent anemia.
Raffaella Origa
exaly   +4 more sources

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Thalassemia

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, Renzo, Galanello, Dudley J, Pennell, Melody J, Cunningham, Elliott, Vichinsky   +4 more
openaire   +2 more sources