Saglio G - Search Results

1

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.

Ottolenghi S, Camaschella C, Comi P, Giglioni B, Longinotti M, Oggiano L, Dore F, Sciarratta G, Ivaldi G, Saglio G, et al. Ottolenghi S, et al. Among authors: saglio g. Hum Genet. 1988 May;79(1):13-7. doi: 10.1007/BF00291702. Hum Genet. 1988. PMID: 2452784

2

Molecular diagnosis of A gamma hereditary persistence of fetal hemoglobin using polymerase chain reaction and oligonucleotide analysis.

Gottardi E, Alfarano A, Serra A, Sciarratta G, Bertero MT, Saglio G, Camaschella C. Gottardi E, et al. Among authors: saglio g. Haematologica. 1990 Jan-Feb;75(1):17-20. Haematologica. 1990. PMID: 1692560

3

Deletion and non deletion hereditary persistence of fetal hemoglobin in Italy.

Camaschella C, Serra A, Alfarano A, Gottardi E, Revello D, Bertero MT, Oggiano L, Longinotti M, Saglio G. Camaschella C, et al. Among authors: saglio g. Haematologica. 1990 Sep-Oct;75 Suppl 5:26-30. Haematologica. 1990. PMID: 1707848 No abstract available.

4

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.

Ricco G, Mazza U, Turi RM, Pich PG, Camaschella C, Saglio G, Bernini LF. Ricco G, et al. Among authors: saglio g. Hum Genet. 1976 Jun 29;32(3):305-13. doi: 10.1007/BF00295821. Hum Genet. 1976. PMID: 939551

5

Rapid identification by denaturing gradient gel electrophoresis of mutations in the gamma-globin gene promoters in non-deletion type HPFH.

Gottardi E, Losekoot M, Fodde R, Saglio G, Camaschella C, Bernini LF. Gottardi E, et al. Among authors: saglio g. Br J Haematol. 1992 Apr;80(4):533-8. doi: 10.1111/j.1365-2141.1992.tb04569.x. Br J Haematol. 1992. PMID: 1374633

6

Screening for mutations in the phenylalanine hydroxylase gene from Italian patients with phenylketonuria by using the chemical cleavage method: a new splice mutation.

Dianzani I, Forrest SM, Camaschella C, Saglio G, Ponzone A, Cotton RG. Dianzani I, et al. Among authors: saglio g. Am J Hum Genet. 1991 Mar;48(3):631-5. Am J Hum Genet. 1991. PMID: 1671810 Free PMC article.

7

A new hereditary persistence of fetal hemoglobin deletion has the breakpoint within the 3' beta-globin gene enhancer.

Camaschella C, Serra A, Gottardi E, Alfarano A, Revello D, Mazza U, Saglio G. Camaschella C, et al. Among authors: saglio g. Blood. 1990 Feb 15;75(4):1000-5. Blood. 1990. PMID: 1689188 Free article.

8

Haplotype distribution and molecular defects at the phenylalanine hydroxylase locus in Italy.

Dianzani I, Devoto M, Camaschella C, Saglio G, Ferrero GB, Cerone R, Romano C, Romeo G, Giovannini M, Riva E, et al. Dianzani I, et al. Among authors: saglio g. Hum Genet. 1990 Nov;86(1):69-72. doi: 10.1007/BF00205176. Hum Genet. 1990. PMID: 1979309

9

Heterogeneity of molecular defects underlying hereditary persistence of fetal hemoglobin in Mediterranean area.

Ottolenghi S, Giglioni B, Casini C, Merli S, Mantovani R, Comi P, Serra A, Guerrasio A, Camaschella C, Saglio G. Ottolenghi S, et al. Among authors: saglio g. Prog Clin Biol Res. 1985;191:151-61. Prog Clin Biol Res. 1985. PMID: 2413471 Review. No abstract available.

10

Italian type of deletional hereditary persistence of fetal hemoglobin.

Saglio G, Camaschella C, Serra A, Bertero T, Rege Cambrin G, Guerrasio A, Mazza U, Izzo P, Terragni F, Giglioni B, et al. Saglio G, et al. Blood. 1986 Sep;68(3):646-51. Blood. 1986. PMID: 2427137 Free article.

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