C. Panarello

发表

Meiotic origin of trisomy in neoplasms: evidence in a case of erythroleukaemia

E. Lanino, C. Olivieri, C. Danesino, 2001, Leukemia.

Lipoblastoma: a case with t(7;8)(q31;q13).

N. Archidiacono, M. Rocchi, A. Ricco, 1998, Cancer genetics and cytogenetics.

t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia.

C. Micalizzi, C. Rosanda, E. Tassano, 2005, Leukemia research.

Evidence of involvement of the PLAG1 gene in lipoblastomas.

J. Mark, G. Stenman, L. Sainati, 2000, International journal of oncology.

Is t(10;11)(p11.2;q23) involving MLL and ABI-1 genes associated with congenital acute monocytic leukemia?

C. Micalizzi, C. Rosanda, C. Morerio, 2002, Cancer genetics and cytogenetics.

Short communication Is t(10;11)(p11.2;q23) involving MLL and ABI-1 genes associated with congenital acute monocytic leukemia?

C. Micalizzi, C. Rosanda, C. Morerio, 2002 .

Refractory cytopenia of childhood with monosomy 7 presenting as isolated neutropenia in a patient with fragile site at 16q22.

C. Micalizzi, E. Tassano, C. Morerio, 2010, Cancer genetics and cytogenetics.

XY female with a dysgerminoma and no mutation in the coding sequence of the SRY gene.

V. Calvari, C. Gambini, C. Rosanda, 2002, Cancer genetics and cytogenetics.

17q21-qter trisomy is an indicator of poor prognosis in acute myelogenous leukemia.

G. Basso, F. Pasquali, E. Maserati, 2001, Cancer genetics and cytogenetics.

MLLT10 (myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10)

C. Morerio, C. Panarello, 2011 .

Gain of 1q in pediatric myelodysplastic syndromes.

E. Lanino, C. Micalizzi, C. Rosanda, 2006, Leukemia research.

Early occurrence of a secondary thyroid carcinoma in a child treated for Hodgkin disease.

C. Gambini, A. Garaventa, C. Panarello, 2001, Medical and pediatric oncology.

Monitoring the Isochromosome i(7)(q10) in the Bone Marrow of Patients With Shwachman Syndrome by Real-time Quantitative PCR

F. Locatelli, R. Valli, B. Pressato, 2007, Journal of pediatric hematology/oncology.

Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies

C. Mecucci, G. Menna, C. Danesino, 2006, Genes, chromosomes & cancer.

Trisomy 17 in congenital plexiform (multinodular) cellular schwannoma.

A. Garaventa, A. Sementa, E. Tassano, 2010, Cancer genetics and cytogenetics.

Differential diagnosis of lipoma‐like lipoblastoma

C. Granata, M. Conte, C. Rosanda, 2009, Pediatric blood & cancer.

MLL-MLLT10 fusion gene in pediatric acute megakaryoblastic leukemia.

C. Rosanda, E. Tassano, C. Morerio, 2005, Leukemia research.

MLL-MLLT10 fusion in acute monoblastic leukemia: variant complex rearrangements and 11q proximal breakpoint heterogeneity.

E. Lanino, A. Di Cataldo, F. Pasquali, 2004, Cancer genetics and cytogenetics.

Inversion (11)(p15q22) with NUP98-DDX10 fusion gene in pediatric acute myeloid leukemia.

C. Rosanda, E. Tassano, C. Morerio, 2006, Cancer genetics and cytogenetics.

Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52.

G. Gimelli, D. Caprino, P. Mori, 1992, Cytogenetics and cell genetics.

A further case of chromosome 8q rearrangement in lipoblastoma.

C. Gambini, C. Rosanda, A. Rizzo, 2000, Journal of pediatric hematology/oncology.

PLAG1-HAS2 fusion in lipoblastoma with masked 8q intrachromosomal rearrangement.

C. Gambini, C. Rosanda, E. Tassano, 2005, Cancer genetics and cytogenetics.

Cytogenetic characterization of a fibrous hamartoma of infancy with complex translocations.

A. Garaventa, E. Tassano, C. Morerio, 2010, Cancer genetics and cytogenetics.

Soft tissue tumors: Lipoblastoma

C. Morerio, C. Panarello, 2011 .

Full cytogenetic characterization of a new neuroblastoma cell line with a complex 17q translocation.

A. Morando, F. Pasquali, M. Corrias, 2000, Cancer genetics and cytogenetics.

Variant Philadelphia translocations in CML: correlation with fragile sites.

P. Mandich, F. Frassoni, R. Defferrari, 1988, Cancer genetics and cytogenetics.

Cryptic translocation t(5;11)(q35;p15.5) with involvement of the NSD1 and NUP98 genes without 5q deletion in childhood acute myeloid leukemia

C. Rosanda, C. Morerio, C. Panarello, 2002, Genes, chromosomes & cancer.

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

P. Cornaglia-Ferraris, R. Sansone, M. Garrè, 1989, Acta haematologica.

Short communication Inversion (11)(p15q22) with NUP98eDDX10 fusion gene in pediatric acute myeloid leukemia

C. Rosanda, E. Tassano, C. Morerio, 2006 .

Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498)

F. Locatelli, R. Valli, B. Pressato, 2008, Haematologica.

Karyotype evolution in CML: high frequency of translocations other than the Ph.

D. Coviello, F. Ajmar, M. Sessarego, 1987, Cancer genetics and cytogenetics.

HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t(5;17)(q33;p11.2).

F. Locatelli, F. Pasquali, E. Maserati, 2004, Cancer research.

G-Bands without pretreatment of slides, in chemically defined conditions

G. Gimelli, F. Bignone, C. Panarello, 2004, Human Genetics.

Acute myelogenous leukemia with translocation t(8;21): a cytogenetic study of seven cases.

F. Frassoni, C. Mareni, F. Ajmar, 1986, Cancer genetics and cytogenetics.

The isochromosome (17q) in chronic myelocytic leukaemia: Mechanism of origin, centromeric function and clonal evolution

F. Pasquali, P. Bernasconi, R. Casalone, 2004, Human Genetics.

Prognostic impact of t(9;11) in childhood acute myeloid leukemia (AML)

G. Schilirò, L. L. Nigro, C. Morerio, 2003, Leukemia.

MicroRNA‐125b‐1 and BLID upregulation resulting from a novel IGH translocation in childhood B‐Cell precursor acute lymphoblastic leukemia

Concetta Micalizzi, C. Micalizzi, Elisa Tassano, 2010, Genes, chromosomes & cancer.

Differential diagnosis of congenital fibrosarcoma.

C. Gambini, M. Conte, C. Rosanda, 2004, Cancer genetics and cytogenetics.