IRIS

Sfoglia per Autore  CAMASCHELLA, CLARA

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The relationship between anemia, fecal stercobilinogen erythrocyte survival, and globin synthesis in heterozygotes for beta-thalassemia 1-gen-1975 Gallo, E; Pich, P; Ricco, G; Saglio, G; Camaschella, Clara; Mazza, U.
Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine replaced by threonine at position 75 )E 19) of the gamma chain 1-gen-1976 Ricco, G; Mazza, U; Turi, Rm; Pich, Pg; Camaschella, Clara; Saglio, G; Bernini, Lf
Interaction between Hb Hasharon and alpha-thalassemia: an approach to the problem of the number of human alpha loci 1-gen-1978 Pich, P; Saglio, G; Camaschella, Clara; David, O; Vasino, Ma; Ricco, G; Mazza, U.
G gamma and A gamma globin chains separation and quantitation by isoelectric focusing 1-gen-1979 Comi, P; Giglioni, B; Ottolenghi, S; Gianni, Am; Ricco, G; Mazza, U; Saglio, G; Camaschella, Clara; Pich, Pg; Gianazza, E; Righetti, Pg
Human T gamma globin chain is a variant of A gamma chain (A gamma Sardinia) 1-gen-1979 Saglio, G; Ricco, G; Mazza, U; Camaschella, Clara; Pich, Pg; Gianni, Am; Gianazza, E; Righetti, Pg; Giglioni, B; Comi, P; Gusmeroli, M; Ottolenghi, S.
gamma chain composition in five Italian newborns heterozygous for Hb F Malta G gamma-117 His leads to Arg. 1-gen-1980 Mazza, U; Meloni, T; David, O; Pich, Pg; Camaschella, Clara; Saglio, G; Ciocca Vasino, Ma; Guerrasio, A; Ricco, G.
Thoracic extramedullary hematopoiesis in thalassemia intermedia during adult life: a report of 9 cases. 1-gen-1981 Camaschella, Clara; Saglio, G; Pich, Pg; Canavoso, P; Ferraris, R; Bianco, G; Mazza, U.
G gamma and a gamma globin chain synthesis in bone marrow and peripheral blood of beta-thalassaemia homozygotes. 1-gen-1982 Saglio, G; Camaschella, Clara; Guerrasio, A; Cambrin, Gr; Capaldi, A; Pich, Pg; Trento, M; Mazza, U.
Molecular comparison of delta beta-thalassemia and hereditary persistence of fetal hemoglobin DNAs: evidence of a regulatory area? 1-gen-1982 Ottolenghi, S; Giglioni, B; Taramelli, R; Comi, P; Mazza, U; Saglio, G; Camaschella, Clara; Izzo, P; Cao, A; Galanello, R; Gimferrer, E; Baiget, M; Gianni, Am
A molecular study of a family with Greek hereditary persistence of fetal hemoglobin and beta-thalassemia. 1-gen-1984 Giglioni, B; Casini, C; Mantovani, R; Merli, S; Comi, P; Ottolenghi, S; Saglio, G; Camaschella, Clara; Mazza, U.
The beta-globin gene in Sardinian delta beta 0-thalassemia carries a C----T nonsense mutation at codon 39. 1-gen-1984 Guida, S; Giglioni, B; Comi, P; Ottolenghi, S; Camaschella, Clara; Saglio, G.
Fetal diagnosis of beta-thalassaemia by DNA analysis in Italy 1-gen-1986 Camaschella, Clara; Saglio, G; Serra, A; Cremonesi, L; Travi, M; Ferrari, Maurizio
Molecular characterization and hematological phenotype of Sicilian delta beta-thalassemia 1-gen-1986 Camaschella, Clara; Serra, A; Bertero, Mt; Trento, M; Dall'Acqua, M; Gottardi, E; Izzo, P; Brancati, C; Mazza, U.
Italian type of deletional hereditary persistence of fetal hemoglobin. 1-gen-1986 Saglio, G; Camaschella, Clara; Serra, A; Bertero, T; Rege Cambrin, G; Guerrasio, A; Mazza, U; Izzo, P; Terragni, F; Giglioni, B.
Sardinian delta beta zero-thalassemia: a further example of a C to T substitution at position -196 of the A gamma globin gene promoter. 1-gen-1987 Ottolenghi, S; Giglioni, B; Pulazzini, A; Comi, P; Camaschella, Clara; Serra, A; Guerrasio, A; Saglio, G.
A benign form of thalassaemia intermedia may be determined by the interaction of triplicated alpha locus and heterozygous beta-thalassaemia 1-gen-1987 Camaschella, Clara; Bertero, Mt; Serra, A; Dall'Acqua, M; Gasparini, P; Trento, M; Vettore, L; Perona, G; Saglio, G; Mazza, U.
Meiotic recombination in the beta globin gene cluster causing an error in prenatal diagnosis of beta thalassaemia 1-gen-1988 Camaschella, Clara; Serra, A; Saglio, G; Bertero, Mt; Mazza, U; Terzoli, S; Brambati, B; Cremonesi, L; Travi, M; Ferrari, Maurizio
Delineation of specific beta-thalassemia mutations in high-risk areas of Italy: a prerequisite for prenatal diagnosis. 1-gen-1988 Pirastu, M; Saglio, G; Camaschella, Clara; Loi, A; Serra, A; Bertero, T; Gabutti, W; Cao, A.
A frequent A gamma-hereditary persistence of fetal hemoglobin in northern Sardinia: its molecular basis and hematologic phenotype in heterozygotes and compound heterozygotes with beta-thalassemia 1-gen-1988 Ottolenghi, S; Camaschella, Clara; Comi, P; Giglioni, B; Longinotti, M; Oggiano, L; Dore, F; Sciarratta, G; Ivaldi, G; Saglio, G.
Circulating 'trophoblast' cells in pregnancy have maternal genetic markers 1-gen-1989 Bertero, Mt; Camaschella, Clara; Serra, A; Bergui, L; Caligaris Cappio, F.
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