Saglio G - Search Results

1

Persistence of E2A/PBX1 transcripts in t(1;19) childhood acute lymphoblastic leukemia: correlation with chemotherapy intensity and clinical outcome.

Lanza C, Gottardi E, Gaidano G, Vivenza C, Parziale A, Perfetto F, Fornaci M, Barisone E, Madon E, Basso G, Saglio G. Lanza C, et al. Among authors: saglio g. Leuk Res. 1996 May;20(5):441-3. doi: 10.1016/0145-2126(95)00115-8. Leuk Res. 1996. PMID: 8683984

2

A new TaqI polymorphism in the p53 gene.

Serra A, Gaidano GL, Revello D, Guerrasio A, Ballerini P, Dalla Favera R, Saglio G. Serra A, et al. Among authors: saglio g. Nucleic Acids Res. 1992 Feb 25;20(4):928. doi: 10.1093/nar/20.4.928. Nucleic Acids Res. 1992. PMID: 1347421 Free PMC article.

3

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

4

Minimal residual disease status in transplanted chronic myelogenous leukemia patients: low incidence of polymerase chain reaction positive cases among 48 long disease-free subjects who received unmanipulated allogeneic bone marrow transplants.

Guerrasio A, Martinelli G, Saglio G, Rosso C, Zaccaria A, Rosti G, Testoni N, Ambrosetti A, Izzi T, Sessarego M, et al. Guerrasio A, et al. Among authors: saglio g. Leukemia. 1992 Jun;6(6):507-12. Leukemia. 1992. PMID: 1602789

5

Transient cytogenetic relapse in a Ph1-positive chronic myelogenous leukemia patient previously treated with alpha-interferon.

Rege-Cambrin G, Guerrasio A, Scaravaglio P, Rosso C, Carozzi F, Kerim S, Saglio G. Rege-Cambrin G, et al. Among authors: saglio g. Leukemia. 1992 Jul;6(7):738-41. Leukemia. 1992. PMID: 1625497

6

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.

7

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

8

Prenatal diagnosis of fetal hemoglobin Lepore-Boston disease on maternal peripheral blood.

Camaschella C, Alfarano A, Gottardi E, Travi M, Primignani P, Caligaris Cappio F, Saglio G. Camaschella C, et al. Among authors: saglio g. Blood. 1990 Jun 1;75(11):2102-6. Blood. 1990. PMID: 1693293 Free article.

9

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.

10

Extra translocation +der(1q9p) is a prognostic indicator in myeloproliferative disorders.

Rege-Cambrin G, Speleman F, Kerim S, Scaravaglio P, Carozzi F, Dal Cin P, Michaux JL, Offner F, Saglio G, Van den Berghe H. Rege-Cambrin G, et al. Among authors: saglio g. Leukemia. 1991 Dec;5(12):1059-63. Leukemia. 1991. PMID: 1774954 Review.

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