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Indian Journal of Pediatrics|November 1, 1989
Prenatal diagnosis of inherited hemoglobinopathiesA Cao, C Rosatelli, R Galanello, et al.
Hemoglobin|January 1, 1984
Hemoglobin constitution of double heterozygotes for alpha or beta-thalassemia and Hb J SardegnaL Maccioni, R Galanello, M A Melis, et al.
Science (New York, N.Y.)|March 2, 1984
Multiple mutations produce delta beta 0 thalassemia in SardiniaM Pirastu, Y W Kan, R Galanello, et al.
British Journal of Haematology|July 1, 1986
Molecular pathology of haemoglobin H disease in SardiniansE Paglietti, R Galanello, P Moi, et al.
Annals of the New York Academy of Sciences|July 21, 1998
A multi-center safety trial of the oral iron chelator deferiproneA Cohen, R Galanello, A Piga, et al.
Hemoglobin|March 18, 2000
Hb Sallanches [alpha104(G11)Cys-->Tyr]: a rare alpha2-globin chain variant found in the homozygous state in three members of a Pakistani familyS N Khan, F I Butt, S Riazuddin, et al.
British Journal of Haematology|October 1, 1984
Alpha thalassaemia in Sardinian newbornsR Galanello, L Maccioni, R Ruggeri, et al.
Archives of Internal Medicine|August 1, 1975
Heart block and hyperthyroidism. Report of two casesS Campus, A Rappelli, A Malavasi, et al.
Dermatologica|January 1, 1978
Scintigraphic evaluation of Kaposi's sarcomaG Madeddu, G Borroni, G Rabbiosi, et al.
Pediatric Research|February 1, 1984
Longitudinal study of a newborn with a combination of deletion and nondeletion alpha-thalassemia-2R Galanello, M A Melis, L Maccioni, et al.
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