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Haematologica|July 1, 1989
The effect of the beta thalassemia mutation on the clinical severity of the sickle beta thalassemia syndromeL Perseu, M S Ristaldi, S P Dibenedetto, et al.Acta Haematologica|January 1, 1980
Hematological characteristics of sardinian alpha-thalassemia carriers detected in a population studyM A Melis, C Rosatelli, A M Falchi, et al.The New England Journal of Medicine|August 4, 1983
Prenatal diagnosis of beta-thalassemia. Detection of a single nucleotide mutation in DNAM Pirastu, Y W Kan, A Cao, et al.British Journal of Haematology|September 1, 1999
Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesisM Cazzola, Y Beguin, G Bergamaschi, et al.British Journal of Haematology|May 1, 1993
Normal individuals with high Hb A2 levelsD Gasperini, A Cao, L Paderi, et al.British Journal of Haematology|February 15, 2002
Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemiaR Galanello, S Piras, S Barella, et al.Cognition|July 22, 2022
Predicting visual memory across images and within individualsCheyenne D Wakeland-Hart, Steven A Cao, Megan T deBettencourt, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1981
Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levelsR Galanello, M A Melis, M Furbetta, et al.Pathologica|October 13, 2000
[Histological picture of liver disease in thalassemia intermedia]M G Mancosu, R Galanello, R Ambu, et al.Pageof 37