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Annals of the New York Academy of Sciences|January 1, 1990
Antenatal diagnosis of beta-thalassemia in SardiniaA Cao, M C Rosatelli, G B Leoni, et al.American Journal of Hematology|December 5, 1998
Alpha-thalassemia carrier identification by DNA analysis in the screening for thalassemiaR Galanello, C Sollaino, E Paglietti, et al.Blood|January 15, 1994
Serum erythropoietin and erythropoiesis in high- and low-fetal hemoglobin beta-thalassemia intermedia patientsR Galanello, S Barella, M P Turco, et al.Annals of the New York Academy of Sciences|December 13, 2005
Osteoporosis in beta-thalassemia: Clinical and genetic aspectsR Origa, E Fiumana, M R Gamberini, et al.British Journal of Haematology|December 31, 1997
Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndromeR Galanello, L Perseu, M A Melis, et al.Human Genetics|May 1, 1992
Human alpha-globin gene expression is silenced by terminal truncation of chromosome 16p beginning immediately 3' of the zeta-globin geneL Romao, F Cash, I Weiss, et al.American Journal of Hematology|June 1, 1994
Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screeningR Galanello, S Barella, A Ideo, et al.The Journal of Automatic Chemistry|January 1, 1995
Evaluation of an automatic HPLC analyser for thalassemia and haemoglobin variants screeningR Galanello, S Barella, D Gasperini, et al.Acta Haematologica|January 1, 1992
HbH disease in Sardinia: molecular, hematological and clinical aspectsR Galanello, B Aru, C Dessì, et al.Human Genetics|March 1, 1995
Variability of the immunoglobulin heavy chain constant region locus: a population studyA Brusco, U Cariota, A Bottaro, et al.Pageof 12