Valetto A - Search Results

1

Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis.

Lanciotti M, Perutelli P, Valetto A, Di Martino D, Mori PG. Lanciotti M, et al. Among authors: valetto a. Haematologica. 1997 Jul-Aug;82(4):460-2. Haematologica. 1997. PMID: 9299863 No abstract available.

2

Inversion mutation as a major cause of severe hemophilia A in Italian patients.

Mori PG, Caprino D, Bicocchi MP, Valetto A, Bottini F, Aquila M. Mori PG, et al. Among authors: valetto a. Haematologica. 1997 Jan-Feb;82(1):75-6. Haematologica. 1997. PMID: 9107090

3

Rapid detection of gammaT cell receptor gene rearrangements in acute lymphoblastic leukemia by electrophoresis and silver staining: implications for detection of minimal residual disease.

Valetto A, Lanciotti M, Di Martino D, Anselmi G, Bottini F, Mori P, Candiano G. Valetto A, et al. Electrophoresis. 1998 Jun;19(8-9):1385-7. doi: 10.1002/elps.1150190831. Electrophoresis. 1998. PMID: 9694286

4

Late Epstein-Barr virus infection of a hepatosplenic gamma delta T-cell lymphoma arising in a kidney transplant recipient.

Roncella S, Cutrona G, Truini M, Airoldi I, Pezzolo A, Valetto A, Di Martino D, Dadati P, De Rossi A, Ulivi M, Fontana I, Nocera A, Valente U, Ferrarini M, Pistoia V. Roncella S, et al. Among authors: valetto a. Haematologica. 2000 Mar;85(3):256-62. Haematologica. 2000. PMID: 10702813

5

A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy.

Acquila M, Bicocchi MP, Mori PG, Odino S, Valetto A, Bottini F. Acquila M, et al. Among authors: valetto a. Eur J Haematol. 2000 Jul;65(1):80-1. doi: 10.1034/j.1600-0609.2000.9l140.x. Eur J Haematol. 2000. PMID: 10914946 No abstract available.

6

Use of molecular techniques to confirm true re-emergence of the original clone and to track minimal residual disease in a case of late extramedullary relapse of childhood acute lymphoblastic leukemia.

Valetto A, Anselmi G, Scuderi F, Lanciotti M, Chiesa V, Dini G. Valetto A, et al. Haematologica. 2000 Oct;85(10):1102-3. Haematologica. 2000. PMID: 11025609 No abstract available.

7

Detection of T cell receptor delta gene rearrangements in childhood B and T lineage acute lymphoblastic leukaemia by southern blot and PCR: technical comparison of two methods of analysis.

Valetto A, Di Martino D, Scuderi F, Lanza T, Lanciotti M, Bottini F, Dini G. Valetto A, et al. Clin Lab Haematol. 2000 Oct;22(5):263-9. doi: 10.1046/j.1365-2257.2000.00317.x. Clin Lab Haematol. 2000. PMID: 11122266

8

A new strategy for prenatal diagnosis in a sporadic haemophilia B family.

Acquila M, Bottini F, Valetto A, Caprino D, Mori PG, Bicocchi MP. Acquila M, et al. Among authors: valetto a. Haemophilia. 2001 Jul;7(4):416-8. doi: 10.1046/j.1365-2516.2001.00514.x. Haemophilia. 2001. PMID: 11442646

9

Non-identical twin sisters concordant for Langerhans cell histiocytosis and discordant for secondary acute promyelocytic leukemia.

Dufour C, Lanciotti M, Micalizzi C, Valetto A, Haupt R. Dufour C, et al. Among authors: valetto a. Med Pediatr Oncol. 2001 Jul;37(1):70-2. doi: 10.1002/mpo.1169. Med Pediatr Oncol. 2001. PMID: 11466730 No abstract available.

10

B-cell repertoire reconstitution after hematopoietic stem cell transplantation in children evaluated by immunoglobulin heavy chain third complementarity determining region fingerprinting.

Di Martino D, Dallorso S, Terranova P, Scarso L, Morreale G, Valetto A. Di Martino D, et al. Among authors: valetto a. Haematologica. 2004 Apr;89(4):506-8. Haematologica. 2004. PMID: 15075092

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