Haupt R - Search Results

1

Karyotype evolution in a patient with biphenotypic neonatal leukemia.

Fugazza G, Basso G, Sessarego M, Haupt R, Comelli A, Roncella S, Negri D, Sansone R. Fugazza G, et al. Among authors: haupt r. Cancer Genet Cytogenet. 1992 Sep;62(2):124-9. doi: 10.1016/0165-4608(92)90249-8. Cancer Genet Cytogenet. 1992. PMID: 1394096

2

Pentasomy 21 in leukemia complicating Diamond-Blackfan anemia.

Mori PG, Haupt R, Fugazza G, Sessarego M, Corcione A, Strigini P, Sansone R. Mori PG, et al. Among authors: haupt r. Cancer Genet Cytogenet. 1992 Oct 1;63(1):70-2. doi: 10.1016/0165-4608(92)90067-i. Cancer Genet Cytogenet. 1992. PMID: 1423230

3

Secondary acute promyelocytic leukemia with t(8;21) and t(9;22) at onset and loss of the Philadelphia chromosome at relapse.

Dallorso S, Sessarego M, Garré ML, Haupt R, Pasino M, Sansone R. Dallorso S, et al. Among authors: haupt r. Cancer Genet Cytogenet. 1990 Jul 1;47(1):41-6. doi: 10.1016/0165-4608(90)90260-h. Cancer Genet Cytogenet. 1990. PMID: 2357686

4

ins(6;1) in a patient with congenital leukemia.

Sansone R, Sessarego M, Haupt R, Garré ML, Strigini P. Sansone R, et al. Among authors: haupt r. Cancer Genet Cytogenet. 1989 Jan;37(1):19-22. doi: 10.1016/0165-4608(89)90069-1. Cancer Genet Cytogenet. 1989. PMID: 2917330

5

Cytogenetics of infantile leukemias and its correlations with bio-clinical features. The "G. Gaslini" Children's Hospital experience over a 9-year period.

Haupt R, Comelli A, Garré ML, Defferrari R, Fugazza G, Basso G, Rosanda C, Sessarego M, Sansone R. Haupt R, et al. Haematologica. 1991 Mar-Apr;76(2):109-12. Haematologica. 1991. PMID: 1937167

6

Congenital leukemia: persistent spontaneous regression in a patient with an acquired abnormal karyotype.

Sansone R, Haupt R, Strigini P, Garrè ML, Panarello C, Cornaglia-Ferraris P. Sansone R, et al. Among authors: haupt r. Acta Haematol. 1989;81(1):48-50. doi: 10.1159/000205400. Acta Haematol. 1989. PMID: 2494835 Review.

7

Infantile leukemia with a new chromosomal rearrangement involving 11q.

Sansone R, Strigini P, Sessarego M, Haupt R, Cornaglia-Ferraris P. Sansone R, et al. Among authors: haupt r. Cancer Genet Cytogenet. 1988 Jun;32(2):293-4. doi: 10.1016/0165-4608(88)90294-4. Cancer Genet Cytogenet. 1988. PMID: 3163268 No abstract available.

8

Acute myeloid leukemia after single-agent treatment with etoposide for Langerhans' cell histiocytosis of bone.

Haupt R, Comelli A, Rosanda C, Sessarego M, De Bernardi B. Haupt R, et al. Am J Pediatr Hematol Oncol. 1993 May;15(2):255-7. doi: 10.1097/00043426-199305000-00015. Am J Pediatr Hematol Oncol. 1993. PMID: 8498650

9

Genetic polymorphism of NAD(P)H:quinone oxidoreductase is associated with an increased risk of infant acute lymphoblastic leukemia without MLL gene rearrangements.

Lanciotti M, Dufour C, Corral L, Di Michele P, Pigullo S, De Rossi G, Basso G, Leszl A, Luciani M, Lo Nigro L, Micalizzi C, Valsecchi MG, Biondi A, Haupt R. Lanciotti M, et al. Among authors: haupt r. Leukemia. 2005 Feb;19(2):214-6. doi: 10.1038/sj.leu.2403613. Leukemia. 2005. PMID: 15618957

10

[Wilms' tumor, polycythemia, ichthyosis and ear malformations: a new syndrome?].

Haupt R, Sansone R, Dallorso S, Garrè ML, Corciulo P. Haupt R, et al. Pediatr Med Chir. 1992 Mar-Apr;14(2):215-7. Pediatr Med Chir. 1992. PMID: 1324484 Review. Italian.

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