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British Journal of Haematology|November 13, 2001
Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndromeD Girelli, C Bozzini, G Zecchina, et al.
American Journal of Human Genetics|April 1, 1997
Mutation analysis of the HLA-H gene in Italian hemochromatosis patientsM Carella, L D'Ambrosio, A Totaro, et al.
Genomics|February 1, 1996
Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I regionA Totaro, J M Rommens, A Grifa, et al.
Blood|March 15, 1991
Molecular characterization of beta-thalassemia intermedia in patients of Italian descent and identification of three novel beta-thalassemia mutationsS Murru, G Loudianos, M Deiana, et al.
The Italian Journal of Gastroenterology|April 1, 1996
Prolonged treatment of chronic C hepatitis by means of medium-high doses of recombinant alpha-2b interferon: an open study to evaluate response and long-term relapseG P Benetti, G Ramella, A Corbellini, et al.
Genetic Testing|August 23, 2000
A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technologyG Restagno, A M Gomez, L Sbaiz, et al.
American Journal of Hematology|June 1, 1997
Different hematological phenotypes caused by the interaction of triplicated alpha-globin genes and heterozygous beta-thalassemiaC Camaschella, A C Kattamis, D Petroni, et al.
British Journal of Haematology|December 21, 2000
Haemochromatosis in patients with beta-thalassaemia traitA Piperno, R Mariani, C Arosio, et al.
European Journal of Human Genetics : EJHG|February 5, 1998
Juvenile and adult hemochromatosis are distinct genetic disordersC Camaschella, A Roetto, M Cicilano, et al.
American Journal of Human Genetics|April 17, 1999
Juvenile hemochromatosis locus maps to chromosome 1qA Roetto, A Totaro, M Cazzola, et al.
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