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Minerva Chirurgica|October 31, 1977
[Diagnostic laparotomy in Hodgkin's disease]F Rolfo, G Ardizzone, C Camaschella, et al.
British Journal of Haematology|February 1, 1994
Clinical and haematological improvement induced by etidronate in a patient with idiopathic myelofibrosis and osteosclerosisP Sivera, L Cesano, A Guerrasio, et al.
Haematologica|September 8, 1999
The influence of hemochromatosis mutations on iron overload of thalassemia majorF Longo, G Zecchina, L Sbaiz, et al.
Blood Cells, Molecules & Diseases|June 22, 2005
Juvenile hemochromatosis due to G320V/Q116X compound heterozygosity of hemojuvelin in an Irish patientF Daraio, E Ryan, F Gleeson, et al.
The Journal of Pediatrics|December 25, 2007
Natural history of recessive inheritance of DMT1 mutationsA Iolascon, C Camaschella, D Pospisilova, et al.
Human Genetics|November 1, 1994
A new complex polymorphic repeat close to the HLA-A and HLA-E lociA Totaro, A Grifa, A Roetto, et al.
Blood|November 1, 1975
The relationship between anemia, fecal stercobilinogen, erythrocyte survival, and globin synthesis in heterozygotes for beta-thalassemiaE Gallo, P Pich, G Ricco, et al.
The EMBO Journal|April 1, 1984
The beta-globin gene in Sardinian delta beta 0-thalassemia carries a C----T nonsense mutation at codon 39S Guida, B Giglioni, P Comi, et al.
Prenatal Diagnosis|October 1, 1988
Circulating 'trophoblast' cells in pregnancy have maternal genetic markersM T Bertero, C Camaschella, A Serra, et al.
Human Genetics|June 1, 1994
A unique origin for Sicilian (delta beta) (0)-thalassemia in 33 unrelated families and its rapid diagnostic characterization by PCR analysisG Esposito, M Grosso, E Gottardi, et al.
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