R. Bigoni

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Richter's syndrome in a case of atypical chronic lymphocytic leukaemia with the t(11;14)(q13;q32): role for a p53 exon 7 gene mutation

C. de Angeli, A. Cuneo, N. Piva, 1996, British journal of haematology.

Cytogenetic and molecular cytogenetic characterization of 6 new cases of idiopathic hypereosinophilic syndrome.

A. Cuneo, M. Roberti, G. Castoldi, 2000, Haematologica.

Cytogenetic and interphase cytogenetic characterization of atypical chronic lymphocytic leukemia carrying BCL1 translocation.

M. Negrini, F. Bullrich, A. Cuneo, 1997, Cancer research.

Trisomy 12 in chronic lymphocytic leukemia and hairy cell leukemia: a cytogenetic and interphase cytogenetic study.

A. Cuneo, N. Piva, G. Castoldi, 1994, Leukemia & lymphoma.

Clinical importance of interphase cytogenetics detecting occult chromosome lesions in myelodysplastic syndromes with normal karyotype

A. Cuneo, M. Roberti, N. Piva, 2001, Leukemia.

Molecular cytogenetic characterization of marginal zone B-cell lymphoma: correlation with clinicopathologic findings in 14 cases.

M. Negrini, A. Cuneo, M. Roberti, 2001, Haematologica.

Cutaneous vasculitis in non Hodgkin's lymphoma

M. Negrini, F. Bullrich, A. Cuneo, 1994 .

Late appearance of the 11q22.3-23.1 deletion involving the ATM locus in B-cell chronic lymphocytic leukemia and related disorders. Clinico-biological significance.

M. Negrini, A. Cuneo, R. Bigoni, 2002, Haematologica.

Acquired chromosome 11q deletion involving the ataxia teleangiectasia locus in B-cell non-Hodgkin's lymphoma: correlation with clinicobiologic features.

G. Russo, S. Sabbioni, M. Negrini, 2000, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

BCL-1 rearrangements and p53 mutations in atypical chronic lymphocytic leukemia with t(11;14)(q13;q32).

C. de Angeli, A. Cuneo, S. Moretti, 2000, Haematologica.

Differentiation of follicular dendritic sarcoma cells into functional myeloid‐dendritic cell‐like elements

A. Cuneo, R. Bigoni, M. Porta, 2003, European journal of haematology.

Chronic lymphocytic leukemia with 6q− shows distinct hematological features and intermediate prognosis

A. Veronese, M. Negrini, A. Cuneo, 2004, Leukemia.

Characterization of t(11;14) translocation in mantle cell lymphoma by fluorescent in situ hybridization.

C. Croce, M. Negrini, A. Cuneo, 1996, Oncogene.

Exposure to myelotoxic agents and myelodysplasia: case–control study and correlation with clinicobiological findings

C. de Angeli, A. Cuneo, N. Piva, 1998, British journal of haematology.

Interleukin-3 plus interleukin-6 may improve chromosomal analysis of multiple myeloma: cytologic and cytogenetic evidence in thirty-four patients.

A. Cuneo, M. Roberti, N. Piva, 1996, Cancer genetics and cytogenetics.

Chromosome aberrations in atypical chronic lymphocytic leukemia: a cytogenetic and interphase cytogenetic study

M. Negrini, F. Bullrich, A. Cuneo, 1997, Leukemia.

Atypical chronic lymphocytic leukaemia witht(ll;14)(ql3;q32): karyotype evolution and prolymphocytic transformation

N. Piva, S. Moretti, P. Cavazzini, 1995, British journal of haematology.

Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study.

M. Mancini, C. Mecucci, A. Cuneo, 1998, Haematologica.

Malignant Lymphomas BCL-1 rearrangements and p 53 mutations in atypical chronic lymphocytic leukemia with t ( 11 ; 14 ) ( q 13 ; q 32 )

A. Cuneo, S. Moretti, R. Bigoni, 2000 .

Acquired C hromosome 1 1q D eletion I nvolving t he A taxia Teleangiectasia L ocus i n B -Cell N on-Hodgkin's L ymphoma: Correlation W ith C linicobiologic F eatures

G. Russo, S. Sabbioni, M. Negrini, 2000 .

Heterogeneity of lineage involvement by trisomy 8 in myelodysplastic syndrome. A multiparameter analysis combining conventional cytogenetics, DNA in situ hybridization, and bone marrow culture studies.

A. Cuneo, R. Bigoni, F. Fagioli, 1995, Cancer genetics and cytogenetics.

Involvement of erythrocytic and granulomonocytic lineages by trisomy 11 in two cases of acute myelomonocytic leukemia with trilineage myelodysplasia. An interphase cytogenetic study.

A. Cuneo, G. Castoldi, R. Bigoni, 1994, Cancer genetics and cytogenetics.

rHuEpo administration in patients with low‐risk myelodysplastic syndromes: evaluation of erythroid precursors' response by fluorescence in situ hybridization on May–Grunwald–Giemsa‐stained bone marrow samples

A. Cuneo, R. Bigoni, M. Porta, 2002, British journal of haematology.

Dendritic cells in acute promyelocytic leukaemia

A. Cuneo, R. Bigoni, M. Porta, 2001, British journal of haematology.

A. Cuneo, M. Roberti, S. Moretti, 1999, Leukemia.

An unusual case of untreated chronic lymphocytic leukemia patient presenting with Rhodococcus equi bacteriemia

R. Bigoni, M. Rossi, G. Castoldi, 1996, American journal of hematology.

Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype

M. Mancini, C. Mecucci, A. Cuneo, 2002, Leukemia.

Multilineage involvement in the 5q- syndrome: a fluorescent in situ hybridization study on bone marrow smears.

A. Cuneo, M. Roberti, G. Castoldi, 2001, Haematologica.

Fluorescence in situ hybridization for the detection and monitoring of the Ph-positive clone in chronic myelogenous leukemia: comparison with metaphase banding analysis

A. Hagemeijer, A. Cuneo, M. Roberti, 1998, Leukemia.

Four novel non‐random chromosome rearrangements in B‐cell chronic lymphocytic leukaemia: 6p24–25 and 12p12–13 translocations, 4q21 anomalies and monosomy 21

M. Negrini, C. de Angeli, A. Cuneo, 2000, British journal of haematology.

Towards a clinically relevant cytogenetic classification of chronic lymphocytic leukemia and related disorders.

A. Cuneo, G. Castoldi, R. Bigoni, 1998, Haematologica.

Secondary Chromosome Changes in Mantle Cell Lymphoma: Cytogenetic and Fluorescence in situ Hybridization Studies

A. Cuneo, R. Bigoni, R. Milani, 2001, Leukemia & lymphoma.

Cytogenetic profile of lymphoma of follicle mantle lineage: correlation with clinicobiologic features.

F. Birg, H. Döhner, A. Hagemeijer, 1999, Blood.

A novel recurrent translocation t(11;14)(p11;q32) in splenic marginal zone B cell lymphoma

A. Hagemeijer, A. Cuneo, M. Roberti, 2001, Leukemia.

Secondary Chromosome Changes in Mantle Cell Lymphoma: Cytogenetic and Fluorescence In Situ Hybridization Studies

R. Bigoni, 2007 .

BCL-1 rearrangements and p53 mutations in atypical chronic lymphocytic leukemia with t(11;14)(q13;q32).

C. de Angeli, A. Cuneo, S. Moretti, 2000, Haematologica.

Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study.

M. Roberti, N. Piva, R. Bigoni, 1998, Haematologica.