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Hemoglobin|December 22, 1998
Globin chain synthesis analysis by high performance liquid chromatography in the screening of thalassemia syndromesR Galanello, S Satta, M G Pirroni, et al.Journal of Clinical Pathology|December 24, 2008
The role of haemoglobin A(2) testing in the diagnosis of thalassaemias and related haemoglobinopathiesA Mosca, R Paleari, G Ivaldi, et al.Progress in Clinical and Biological Research|January 1, 1989
Interaction between deletion delta-thalassemia and beta zero-thalassemia (codon 39 nonsense mutation) in a Sardinian familyR Galanello, A Podda, M A Melis, et al.Acta Haematologica|January 1, 1984
Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotypeR Galanello, E Paglietti, M A Melis, et al.Haematologica|July 1, 1990
Preliminary experience with the differential pH technique for glucose-6-phosphate dehydrogenase (G6PD) measurement in whole blood: application to an area with high prevalence of thalassaemia and G6PD deficiencyA Mosca, M Paderi, A Sanna, et al.Hemoglobin|January 1, 1992
Normal delta-globin gene sequences in Sardinian nondeletional delta beta-thalassemiaG Loudianos, P Moi, J Lavinha, et al.Journal of Medical Genetics|December 1, 1983
Phenotype-genotype correlation in haemoglobin H disease in childhoodR Galanello, M Pirastu, M A Melis, et al.British Journal of Haematology|February 26, 2000
Safety profile of the oral iron chelator deferiprone: a multicentre studyA R Cohen, R Galanello, A Piga, et al.Haematologica|March 26, 1999
Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemiaR Galanello, M D Cipollina, C Dessì, et al.Blood|July 1, 1983
Phenotypic effect of heterozygous alpha and beta 0-thalassemia interactionM A Melis, M Pirastu, R Galanello, et al.Pageof 12