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Acta Haematologica|November 13, 2009
Deferiprone chelation therapy for thalassemia majorR Galanello, S CampusBritish Journal of Haematology|November 30, 2006
Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypesR Origa, M C Sollaino, N Giagu, et al.Annals of the New York Academy of Sciences|July 21, 1998
Relationship between genotype and phenotype. Thalassemia intermediaR Galanello, A CaoThe Journal of Clinical Investigation|April 1, 1988
Mechanism of Hb F stimulation by S-stage compounds. In vitro studies with bone marrow cells exposed to 5-azacytidine, Ara-C, or hydroxyureaR Galanello, G Stamatoyannopoulos, T PapayannopoulouBailliere'S Clinical Haematology|June 29, 2000
Prenatal diagnosis and screening of the haemoglobinopathiesA Cao, R Galanello, M C RosatelliCiba Foundation Symposium|January 1, 1996
Control of beta-thalassaemia by carrier screening, genetic counselling and prenatal diagnosis: the Sardinian experienceA Cao, M C Rosatelli, R GalanelloHemoglobin|March 18, 2000
Identification of three rare beta-thalassemia mutations in the Pakistani populationS N Khan, S Riazuddin, R GalanelloBritish Journal of Haematology|April 1, 1983
Alpha globin gene analysis in a Sardinian family with interacting alpha and beta thalassaemia genesM A Melis, R Galanello, A CaoBlood Reviews|March 1, 1994
Genotype-phenotype correlations in beta-thalassemiasA Cao, R Galanello, M C RosatelliPageof 12