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Nouvelle Revue Francaise D'Hematologie|January 1, 1981
Globin chain synthesis analysis in obligate beta 0-thalassemia heterozygotes with isolated increase of hemoglobin A2 levelsR Galanello, M A Melis, M Furbetta, et al.
British Journal of Haematology|September 1, 1999
Soluble transferrin receptor as a potential determinant of iron loading in congenital anaemias due to ineffective erythropoiesisM Cazzola, Y Beguin, G Bergamaschi, et al.
British Journal of Haematology|May 1, 1993
Normal individuals with high Hb A2 levelsD Gasperini, A Cao, L Paderi, et al.
British Journal of Haematology|February 15, 2002
Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemiaR Galanello, S Piras, S Barella, et al.
American Journal of Hematology|October 1, 1988
Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin geneR Galanello, E Paglietti, M A Melis, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|July 1, 1987
The euglycemic clamp in patients with thalassaemia intermediaS Brianda, M Maioli, T Frulio, et al.
Acta Endocrinologica|December 1, 1980
Alteration of thyroid function in the early stage of subacute thyroiditisG Madeddu, M Langer, C Costanza, et al.
British Journal of Haematology|June 1, 1995
A promoter mutation, C-->T at position -92, leading to silent beta-thalassaemiaM C Rosatelli, V Faà, A Meloni, et al.
British Journal of Haematology|August 1, 1989
Erythropoiesis following bone marrow transplantation from donors heterozygous for beta-thalassaemiaR Galanello, S Barella, L Maccioni, et al.
Haematologica|November 1, 1994
Interferon-alpha 2a therapy in CML: disappearance of BCR/ABL transcript in a case of long-lasting continuous cytogenetic conversionS Pardini, M Addis, F Dore, et al.
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