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Respiration; International Review of Thoracic Diseases|January 1, 1980
Relationship between chronic PaCO2 and total body buffering capacity in patients with chronic obstructive lung diseaseG Rizzato, A Ferrara, L Bertoli, et al.
Haematologica|May 1, 1992
Molecular characterization and functional studies on Hb Kempsey, beta 99 (G-1) Asp----Asn, a high-oxygen affinity variantG Ricco, F Scaroina, M C Amprimo, et al.
Cardiologia (Rome, Italy)|December 1, 1995
[Hypertrophic obstructive cardiomyopathy in a patient with Turner syndrome]M R Conte, G Bonfiglio, F Orzan, et al.
Blood|June 1, 1990
Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral bloodC Camaschella, A Alfarano, E Gottardi, et al.
Blood|February 1, 1978
Interaction between Hb Hasharon and alpha-thalassemia: an approach to the problem of the number of human alpha lociP Pich, G Saglio, C Camaschella, et al.
Blood|April 1, 1987
Sardinian delta beta zero-thalassemia: a further example of a C to T substitution at position -196 of the A gamma globin gene promoterS Ottolenghi, B Giglioni, A Pulazzini, et al.
Blood Cells, Molecules & Diseases|August 22, 2000
Exclusion of ZIRTL as candidate gene of juvenile hemochromatosis and refinement of the critical interval on 1q21A Roetto, F Alberti, F Daraio, et al.
Hepatology (Baltimore, Md.)|April 27, 1999
Inherited HFE-unrelated hemochromatosis in Italian familiesC Camaschella, S Fargion, M Sampietro, et al.
Acta Haematologica|January 1, 1979
Biosynthetic studies and gamma-chain composition in the Greek type of hereditary persistence of fetal hemoglobin and in its association with beta-thalassemiaC Camaschella, M A Ciocca-Vasino, A Guerrasio, et al.
Journal of Medical Genetics|March 1, 1993
Molecular analysis of contiguous exons of the phenylalanine hydroxylase gene: identification of a new PKU mutationI Dianzani, C Camaschella, G Saglio, et al.
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