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American Journal of Hematology|January 1, 1992
Heterozygous beta-thalassemia: relationship between the hematological phenotype and the type of beta-thalassemia mutationC Rosatelli, G B Leoni, T Tuveri, et al.Hemoglobin|January 1, 1997
Hb Puttelange [beta 140(H19)Ala-->Val] in an Italian man with polycythemiaR Galanello, R Paleari, L Perseu, et al.Clinical Genetics|November 1, 1990
Fetal hydrops in Sardinia: implications for genetic counsellingR Galanello, M A Sanna, L Maccioni, et al.American Journal of Hematology|January 10, 1998
Heterozygous beta-thalassemia with thalassemia intermedia phenotypeD Gasperini, L Perseu, M A Melis, et al.Pediatric Research|November 1, 1986
Alpha-thalassemia in premature newbornsL Maccioni, R Galanello, R Ruggeri, et al.Molecular Biology & Medicine|July 1, 1983
Globin gene mapping studies in Sardinian patients homozygous for beta zero ThalassaemiaJ S Wainscoat, J I Bell, J M Old, et al.British Journal of Haematology|March 1, 1995
Relationship between transfusion regimen and suppression of erythropoiesis in beta-thalassaemia majorM Cazzola, P De Stefano, L Ponchio, et al.Community Genetics|April 1, 2008
Thalassaemia and glucose-6-phosphate dehydrogenase screening in 13- to 14-year-old students of the Sardinian population: preliminary findingsA Cao, R Congiu, M C Sollaino, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 22, 2000
Elevation of serum creatine kinase as the only manifestation of an intragenic deletion of the dystrophin gene in three unrelated familiesM A Melis, M Cau, F Muntoni, et al.European Heart Journal|February 1, 1987
Massive haemorrhagic pericardial effusion in beta-thalassaemia majorL Cassisa, G DiGirolamo, G Pupita, et al.Pageof 12