Cristina Mecucci

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Cavazzini Francesco; Bardi Antonella; Ciccone Maria; Rigolin Gian Matteo; Gorello Paolo; La Starza Roberta; Mecucci Cristina; Cuneo Antonio
Trisomy 8 in PDGFRB-negative cells in a patient with imatinib-sensitive chronic myelomonocytic leukemia and t(5;16)(q33;p13), PDGFRB-NDE1 fusion.
Haferlach Claudia; Mecucci Cristina; Schnittger Susanne; Kohlmann Alexander; Mancini Marco; Cuneo Antonio; Testoni Nicoletta; Rege-Cambrin Giovanna; Santucci Antonella; Vignetti Marco; Fazi Paola; Martelli Maria Paola; Haferlach Torsten; Falini Brunangelo
AML with mutated NPM1 carrying a normal or aberrant karyotype show overlapping biologic, pathologic, immunophenotypic, and prognostic features.
La Starza Roberta; Brandimarte Lucia; Pierini Valentina; Nofrini Valeria; Gorello Paolo; Crescenzi Barbara; Berchicci Laura; Matteucci Caterina; Romoli Silvia; Beacci Donatella; Rosati Roberto; Martelli Massimo F; Mecucci Cristina
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement.

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2009: Cavazzini Francesco; Bardi Antonella; Ciccone Maria; Rigolin Gian Matteo; Gorello Paolo; La Starza Roberta; Mecucci Cristina; Cuneo Antonio
Trisomy 8 in PDGFRB-negative cells in a patient with imatinib-sensitive chronic myelomonocytic leukemia and t(5;16)(q33;p13), PDGFRB-NDE1 fusion.
Cancer genetics and cytogenetics 2009;194(1):67-9.
2009: Haferlach Claudia; Mecucci Cristina; Schnittger Susanne; Kohlmann Alexander; Mancini Marco; Cuneo Antonio; Testoni Nicoletta; Rege-Cambrin Giovanna; Santucci Antonella; Vignetti Marco; Fazi Paola; Martelli Maria Paola; Haferlach Torsten; Falini Brunangelo
AML with mutated NPM1 carrying a normal or aberrant karyotype show overlapping biologic, pathologic, immunophenotypic, and prognostic features.
Blood 2009;114(14):3024-32.
2009: La Starza Roberta; Brandimarte Lucia; Pierini Valentina; Nofrini Valeria; Gorello Paolo; Crescenzi Barbara; Berchicci Laura; Matteucci Caterina; Romoli Silvia; Beacci Donatella; Rosati Roberto; Martelli Massimo F; Mecucci Cristina
A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement.
Cancer genetics and cytogenetics 2009;193(2):109-11.
2009: Roberti Maria Cristina; La Starza Roberta; Surace Cecilia; Sirleto Pietro; Pinto Rita Maria; Pierini Valentina; Crescenzi Barbara; Mecucci Cristina; Angioni Adriano
RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome.
Virchows Archiv : an international journal of pathology 2009;454(3):311-6.
2009: Morra Enrica; Barosi Giovanni; Bosi Alberto; Ferrara Felicetto; Locatelli Franco; Marchetti Monia; Martinelli Giovanni; Mecucci Cristina; Vignetti Marco; Tura Sante
Clinical management of primary non-acute promyelocytic leukemia acute myeloid leukemia: Practice Guidelines by the Italian Society of Hematology, the Italian Society of Experimental Hematology, and the Italian Group for Bone Marrow Transplantation.
Haematologica 2009;94(1):102-12.
2008: Bousquet Marina; Quelen Cathy; Rosati Roberto; Mansat-De Mas Véronique; La Starza Roberta; Bastard Christian; Lippert Eric; Talmant Pascaline; Lafage-Pochitaloff Marina; Leroux Dominique; Gervais Carine; Viguié Franck; Lai Jean-Luc; Terre Christine; Beverlo Berna; Sambani Costantina; Hagemeijer Anne; Marynen Peter; Delsol Georges; Dastugue Nicole; Mecucci Cristina; Brousset Pierre
Myeloid cell differentiation arrest by miR-125b-1 in myelodysplastic syndrome and acute myeloid leukemia with the t(2;11)(p21;q23) translocation.
The Journal of experimental medicine 2008;205(11):2499-506.
2008: Gorello Paolo; Brandimarte Lucia; La Starza Roberta; Pierini Valentina; Bury Loredana; Rosati Roberto; Martelli Massimo F; Vandenberghe Peter; Wlodarska Iwona; Mecucci Cristina
t(3;11)(q12;p15)/NUP98-LOC348801 fusion transcript in acute myeloid leukemia.
Haematologica 2008;93(9):1398-401.
2008: Aventín Anna; Sánchez Jana; Nomdedéu Josep F; Estany Cristina; Forcada Pilar; La Starza Roberta; Mecucci Cristina
Novel IGHalpha translocations, t(2;14)(q14.3;q32) and t(14;17)(q32;q21), in B-cell precursor acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 2008;185(1):57-9.
2008: Barba Gianluca; Matteucci Caterina; Girolomoni Giampiero; Brandimarte Lucia; Varasano Emanuela; Martelli Massimo Fabrizio; Mecucci Cristina
Comparative genomic hybridization identifies 17q11.2 approximately q12 duplication as an early event in cutaneous T-cell lymphomas.
Cancer genetics and cytogenetics 2008;184(1):48-51.
2008: Lo-Coco Francesco; Cuneo Antonio; Pane Fabrizio; Cilloni Daniela; Diverio Daniela; Mancini Marco; Testoni Nicoletta; Bardi Antonella; Izzo Barbara; Bolli Niccolò; La Starza Roberta; Fazi Paola; Iacobelli Simona; Piciocchi Alfonso; Vignetti Marco; Amadori Sergio; Mandelli Franco; Pelicci Pier Giuseppe; Mecucci Cristina; Falini Brunangelo; Saglio Giuseppe;
Prognostic impact of genetic characterization in the GIMEMA LAM99P multicenter study for newly diagnosed acute myeloid leukemia.
Haematologica 2008;93(7):1017-24.
2008: Falini Brunangelo; Martelli Maria Paola; Mecucci Cristina; Liso Arcangelo; Bolli Niccolò; Bigerna Barbara; Pucciarini Alessandra; Pileri Stefano; Meloni Giovanna; Martelli Massimo F; Haferlach Torsten; Schnittger Susanne
Cytoplasmic mutated nucleophosmin is stable in primary leukemic cells and in a xenotransplant model of NPMc+ acute myeloid leukemia in SCID mice.
Haematologica 2008;93(5):775-9.
2008: Garzon Ramiro; Garofalo Michela; Martelli Maria Paola; Briesewitz Roger; Wang Lisheng; Fernandez-Cymering Cecilia; Volinia Stefano; Liu Chang-Gong; Schnittger Susanne; Haferlach Torsten; Liso Arcangelo; Diverio Daniela; Mancini Marco; Meloni Giovanna; Foa Robin; Martelli Massimo F; Mecucci Cristina; Croce Carlo M; Falini Brunangelo
Distinctive microRNA signature of acute myeloid leukemia bearing cytoplasmic mutated nucleophosmin.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(10):3945-50.
2008: Falini Brunangelo; Mecucci Cristina; Saglio Giuseppe; Lo Coco Francesco; Diverio Daniela; Brown Patrick; Pane Fabrizio; Mancini Marco; Martelli Maria Paola; Pileri Stefano; Haferlach Torsten; Haferlach Claudia; Schnittger Susanne
NPM1 mutations and cytoplasmic nucleophosmin are mutually exclusive of recurrent genetic abnormalities: a comparative analysis of 2562 patients with acute myeloid leukemia.
Haematologica 2008;93(3):439-42.
2008: Matteucci C; Bracci M; Barba G; Carbonari M; Casato M; Visentini M; Pulsoni A; Varasano E; Roti G; La Starza R; Crescenzi B; Martelli M F; Fiorilli M; Mecucci C
Different genomic imbalances in low- and high-grade HCV-related lymphomas.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2008;22(1):219-22.
2008: Gorello P; La Starza R; Brandimarte L; Trisolini S M; Pierini V; Crescenzi B; Limongi M Z; Nanni M; Belloni E; Tapinassi C; Gerbino E; Martelli M F; Foà R; Meloni G; Pelicci P G; Mecucci C
A PDGFRB-positive acute myeloid malignancy with a new t(5;12)(q33;p13.3) involving the ERC1 gene.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2008;22(1):216-8.
2007: Shing Danielle C; Trubia Maurizio; Marchesi Francesco; Radaelli Enrico; Belloni Elena; Tapinassi Cinzia; Scanziani Eugenio; Mecucci Cristina; Crescenzi Barbara; Lahortiga Idoya; Odero Maria D; Zardo Giuseppe; Gruszka Alicja; Minucci Saverio; Di Fiore Pier Paolo; Pelicci Pier Giuseppe
Overexpression of sPRDM16 coupled with loss of p53 induces myeloid leukemias in mice.
The Journal of clinical investigation 2007;117(12):3696-707.
2007: Zhang Ling; Alsabeh Randa; Mecucci Cristina; La Starza Roberta; Gorello Paolo; Lee Stephen; Lill Michael; Schreck Rhona
Rare t(1;11)(q23;p15) in therapy-related myelodysplastic syndrome evolving into acute myelomonocytic leukemia: a case report and review of the literature.
Cancer genetics and cytogenetics 2007;178(1):42-8.
2007: Bolli Niccolò; Nicoletti Ildo; De Marco M Felicetta; Bigerna Barbara; Pucciarini Alessandra; Mannucci Roberta; Martelli Maria Paola; Liso Arcangelo; Mecucci Cristina; Fabbiano Francesco; Martelli Massimo F; Henderson Beric R; Falini Brunangelo
Born to be exported: COOH-terminal nuclear export signals of different strength ensure cytoplasmic accumulation of nucleophosmin leukemic mutants.
Cancer research 2007;67(13):6230-7.
2007: Crescenzi Barbara; La Starza Roberta; Nozzoli Chiara; Ciolli Stefania; Matteucci Caterina; Romoli Silvia; Rigacci Luigi; Gorello Paolo; Bosi Alberto; Martelli Massimo F; Marynen Peter; Mecucci Cristina
Molecular cytogenetic findings in a four-way t(1;12;5;12)(p36;p13;q33;q24) underlying the ETV6-PDGFRB fusion gene in chronic myelomonocytic leukemia.
Cancer genetics and cytogenetics 2007;176(1):67-71.
2007: La Starza Roberta; Crescenzi Barbara; Pierini Valentina; Romoli Silvia; Gorello Paolo; Brandimarte Lucia; Matteucci Caterina; Kropp Maria Grazia; Barba Gianluca; Martelli Massimo Fabrizio; Mecucci Cristina
A common 93-kb duplicated DNA sequence at 1q21.2 in acute lymphoblastic leukemia and Burkitt lymphoma.
Cancer genetics and cytogenetics 2007;175(1):73-6.
2007: Chiaretti Sabina; Tavolaro Simona; Ghia Emanuela Maria; Ariola Cristina; Matteucci Caterina; Elia Loredana; Maggio Roberta; Messina Monica; Ricciardi Maria Rosaria; Vitale Antonella; Ritz Jerome; Mecucci Cristina; Guarini Anna; Foà Robin
Characterization of ABL1 expression in adult T-cell acute lymphoblastic leukemia by oligonucleotide array analysis.
Haematologica 2007;92(5):619-26.
2007: Falini Brunangelo; Nicoletti Ildo; Bolli Niccolò; Martelli Maria Paola; Liso Arcangelo; Gorello Paolo; Mandelli Franco; Mecucci Cristina; Martelli Massimo Fabrizio
Translocations and mutations involving the nucleophosmin (NPM1) gene in lymphomas and leukemias.
Haematologica 2007;92(4):519-32.
2007: La Starza R; Rosati R; Roti G; Gorello P; Bardi A; Crescenzi B; Pierini V; Calabrese O; Baens M; Folens C; Cools J; Marynen P; Martelli M F; Mecucci C; Cuneo A
A new NDE1/PDGFRB fusion transcript underlying chronic myelomonocytic leukaemia in Noonan Syndrome.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2007;21(4):830-3.
2007: Etienne Anne; Gelsi-Boyer Véronique; Carbuccia Nadine; Adélaïde José; Barba Gianluca; La Starza Roberta; Murati Anne; Eclache Virginie; Birg Françoise; Birnbaum Daniel; Mozziconacci Marie-Joëlle; Mecucci Christina; Chaffanet Max
Combined translocation with ZNF198-FGFR1 gene fusion and deletion of potential tumor suppressors in a myeloproliferative disorder.
Cancer genetics and cytogenetics 2007;173(2):154-8.
2007: Crescenzi B; Chase A; Starza R La; Beacci D; Rosti V; Gallì A; Specchia G; Martelli M F; Vandenberghe P; Cools J; Jones A V; Cross N C P; Marynen P; Mecucci C
FIP1L1-PDGFRA in chronic eosinophilic leukemia and BCR-ABL1 in chronic myeloid leukemia affect different leukemic cells.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2007;21(3):397-402.
2007: Rosati Roberto; La Starza Roberta; Barba Gianluca; Gorello Paolo; Pierini Valentina; Matteucci Caterina; Roti Giovanni; Crescenzi Barbara; Aloisi Teresa; Aversa Franco; Martelli Massimo Fabrizio; Mecucci Cristina
Cryptic chromosome 9q34 deletion generates TAF-Ialpha/CAN and TAF-Ibeta/CAN fusion transcripts in acute myeloid leukemia.
Haematologica 2007;92(2):232-5.
2007: Falini Brunangelo; Nicoletti Ildo; Martelli Massimo F; Mecucci Cristina
Acute myeloid leukemia carrying cytoplasmic/mutated nucleophosmin (NPMc+ AML): biologic and clinical features.
Blood 2007;109(3):874-85.
2006: Pasqualucci Laura; Liso Arcangelo; Martelli Maria Paola; Bolli Niccolò; Pacini Roberta; Tabarrini Alessia; Carini Manola; Bigerna Barbara; Pucciarini Alessandra; Mannucci Roberta; Nicoletti Ildo; Tiacci Enrico; Meloni Giovanna; Specchia Giorgina; Cantore Nicola; Di Raimondo Francesco; Pileri Stefano; Mecucci Cristina; Mandelli Franco; Martelli Massimo Fabrizio; Falini Brunangelo
Mutated nucleophosmin detects clonal multilineage involvement in acute myeloid leukemia: Impact on WHO classification.
Blood 2006;108(13):4146-55.
2006: La Starza Roberta; Barba Gianluca; Matteucci Caterina; Crescenzi Barbara; Romoli Silvia; Pierini Valentina; Beacci Donatella; Cantaffa Renato; Martelli Massimo F; Mecucci Cristina
Chronic lymphocytic leukaemia Is terminal del(14)(q24) a new marker for prognostic stratification?
Leukemia research 2006;30(12):1569-72.
2006: Deshpande Aniruddha J; Cusan Monica; Rawat Vijay P S; Reuter Hendrik; Krause Alexandre; Pott Christiane; Quintanilla-Martinez Leticia; Kakadia Purvi; Kuchenbauer Florian; Ahmed Farid; Delabesse Eric; Hahn Meinhard; Lichter Peter; Kneba Michael; Hiddemann Wolfgang; Macintyre Elizabeth; Mecucci Cristina; Ludwig Wolf-Dieter; Humphries R Keith; Bohlander Stefan K; Feuring-Buske Michaela; Buske Christian
Acute myeloid leukemia is propagated by a leukemic stem cell with lymphoid characteristics in a mouse model of CALM/AF10-positive leukemia.
Cancer cell 2006;10(5):363-74.
2006: La Starza Roberta; Crescenzi Barbara; Krause Alexandre; Pierini Valentina; Specchia Giorgina; Bardi Antonella; Nieddu Rosa; Ariola Cristina; Nanni Mauro; Diverio Daniela; Aventin Anna; Sborgia Marco; Martelli Massimo F; Bohlander Stefan K; Mecucci Cristina
Dual-color split signal fluorescence in situ hybridization assays for the detection of CALM/AF10 in t(10;11)(p13;q14-q21)-positive acute leukemia.
Haematologica 2006;91(9):1248-51.
2006: Rosati R; La Starza R; Luciano L; Gorello P; Matteucci C; Pierini V; Romoli S; Crescenzi B; Rotoli B; Martelli M F; Pane F; Mecucci C
TPM3/PDGFRB fusion transcript and its reciprocal in chronic eosinophilic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(9):1623-4.
2006: Falini Brunangelo; Martelli Maria Paola; Bolli Niccolò; Bonasso Rossella; Ghia Emanuela; Pallotta Maria Teresa; Diverio Daniela; Nicoletti Ildo; Pacini Roberta; Tabarrini Alessia; Galletti Barbara Verducci; Mannucci Roberta; Roti Giovanni; Rosati Roberto; Specchia Giorgina; Liso Arcangelo; Tiacci Enrico; Alcalay Myriam; Luzi Lucilla; Volorio Sara; Bernard Loris; Guarini Anna; Amadori Sergio; Mandelli Franco; Pane Fabrizio; Lo-Coco Francesco; Saglio Giuseppe; Pelicci Pier-Giuseppe; Martelli Massimo F; Mecucci Cristina
Immunohistochemistry predicts nucleophosmin (NPM) mutations in acute myeloid leukemia.
Blood 2006;108(6):1999-2005.
2006: Grisendi Silvia; Mecucci Cristina; Falini Brunangelo; Pandolfi Pier Paolo
Nucleophosmin and cancer.
Nature reviews. Cancer 2006;6(7):493-505.
2006: Janssen Hilde; Wlodarska Iwona; Mecucci Cristina; Hagemeijer Anne; Vandenberghe Peter; Marynen Peter; Cools Jan
Fusion of ETV6 to GOT1 in a case with myelodysplastic syndrome and t(10;12)(q24;p13).
Haematologica 2006;91(7):949-51.
2006: La Starza R; Aventin A; Matteucci C; Crescenzi B; Romoli S; Testoni N; Pierini V; Ciolli S; Sambani C; Locasciulli A; Di Bona E; Lafage-Pochitaloff M; Martelli M F; Marynen P; Mecucci C
Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(6):958-64.
2006: Gorello P; Cazzaniga G; Alberti F; Dell'Oro M G; Gottardi E; Specchia G; Roti G; Rosati R; Martelli M F; Diverio D; Lo Coco F; Biondi A; Saglio G; Mecucci C; Falini B
Quantitative assessment of minimal residual disease in acute myeloid leukemia carrying nucleophosmin (NPM1) gene mutations.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(6):1103-8.
2006: Falini Brunangelo; Bolli Niccolò; Shan Jing; Martelli Maria Paola; Liso Arcangelo; Pucciarini Alessandra; Bigerna Barbara; Pasqualucci Laura; Mannucci Roberta; Rosati Roberto; Gorello Paolo; Diverio Daniela; Roti Giovanni; Tiacci Enrico; Cazzaniga Giovanni; Biondi Andrea; Schnittger Suzanne; Haferlach Torsten; Hiddemann Wolfgang; Martelli Massimo F; Gu Wei; Mecucci Cristina; Nicoletti Ildo
Both carboxy-terminus NES motif and mutated tryptophan(s) are crucial for aberrant nuclear export of nucleophosmin leukemic mutants in NPMc+ AML.
Blood 2006;107(11):4514-23.
2006: Roti Giovanni; Rosati Roberto; Bonasso Rossella; Gorello Paolo; Diverio Daniela; Martelli Massimo Fabrizio; Falini Brunangelo; Mecucci Cristina;
Denaturing high-performance liquid chromatography: a valid approach for identifying NPM1 mutations in acute myeloid leukemia.
The Journal of molecular diagnostics : JMD 2006;8(2):254-9.
2006: Roti Giovanni; La Starza Roberta; Ballanti Stelvio; Crescenzi Barbara; Romoli Silvia; Foá Robin; Tartaglia Marco; Aversa Franco; Fabrizio Martelli Massimo; Mecucci Cristina
Acute lymphoblastic leukaemia in Noonan syndrome.
British journal of haematology 2006;133(4):448-50.
2006: van Zutven Laura J C M; Onen Emine; Velthuizen Sandra C J M; van Drunen Ellen; von Bergh Anne R M; van den Heuvel-Eibrink Marry M; Veronese Angelo; Mecucci Cristina; Negrini Massimo; de Greef Georgine E; Beverloo H Berna
Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene.
Genes, chromosomes & cancer 2006;45(5):437-46.
2006: Bolli Niccolò; Galimberti Sara; Martelli Maria P; Tabarrini Alessia; Roti Giovanni; Mecucci Cristina; Martelli Massimo F; Petrini Mario; Falini Brunangelo
Cytoplasmic nucleophosmin in myeloid sarcoma occurring 20 years after diagnosis of acute myeloid leukaemia.
The lancet oncology 2006;7(4):350-2.
2006: Maserati Emanuela; Minelli Antonella; Pressato Barbara; Valli Roberto; Crescenzi Barbara; Stefanelli Maurizio; Menna Giuseppe; Sainati Laura; Poli Furio; Panarello Claudio; Zecca Marco; Curto Francesco Lo; Mecucci Cristina; Danesino Cesare; Pasquali Francesco
Shwachman syndrome as mutator phenotype responsible for myeloid dysplasia/neoplasia through karyotype instability and chromosomes 7 and 20 anomalies.
Genes, chromosomes & cancer 2006;45(4):375-82.
2006: Cimino Giuseppe; Pane Fabrizio; Elia Loredana; Finolezzi Erica; Fazi Paola; Annino Luciana; Meloni Giovanna; Mancini Marco; Tedeschi Alessandra; Di Raimondo Francesco; Specchia Giorgina; Fioritoni Giuseppe; Leoni Pietro; Cuneo Antonio; Mecucci Cristina; Saglio Giuseppe; Mandelli Franco; Foà Robin;
The role of BCR/ABL isoforms in the presentation and outcome of patients with Philadelphia-positive acute lymphoblastic leukemia: a seven-year update of the GIMEMA 0496 trial.
Haematologica 2006;91(3):377-80.
2006: Falini B; Bigerna B; Pucciarini A; Tiacci E; Mecucci C; Morris S W; Bolli N; Rosati R; Hanissian S; Ma Z; Sun Y; Colombo E; Arber D A; Pacini R; La Starza R; Verducci Galletti B; Liso A; Martelli M P; Diverio D; Pelicci P-G; Lo Coco F; Martelli M F
Aberrant subcellular expression of nucleophosmin and NPM-MLF1 fusion protein in acute myeloid leukaemia carrying t(3;5): a comparison with NPMc+ AML.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(2):368-71.
2006: Trubia M; Albano F; Cavazzini F; Cambrin G R; Quarta G; Fabbiano F; Ciambelli F; Magro D; Hernandezo J M; Mancini M; Diverio D; Pelicci P G; Coco F L; Mecucci C; Specchia G; Rocchi M; Liso V; Castoldi G; Cuneo A
Characterization of a recurrent translocation t(2;3)(p15-22;q26) occurring in acute myeloid leukaemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2006;20(1):48-54.
2006: Vitale Antonella; Guarini Anna; Ariola Cristina; Mancini Marco; Mecucci Cristina; Cuneo Antonio; Pane Fabrizio; Saglio Giuseppe; Cimino Giuseppe; Tafuri Agostino; Meloni Giovanna; Fabbiano Francesco; Recchia Anna; Kropp Maria Grazia; Krampera Mauro; Cascavilla Nicola; Ferrara Felicetto; Romano Antonio; Mazza Patrizio; Fozza Claudio; Paoloni Francesca; Vignetti Marco; Foà Robin
Adult T-cell acute lymphoblastic leukemia: biologic profile at presentation and correlation with response to induction treatment in patients enrolled in the GIMEMA LAL 0496 protocol.
Blood 2006;107(2):473-9.
2005: Schnittger Susanne; Schoch Claudia; Kern Wolfgang; Mecucci Cristina; Tschulik Claudia; Martelli Massimo F; Haferlach Torsten; Hiddemann Wolfgang; Falini Brunangelo
Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype.
Blood 2005;106(12):3733-9.
2005: Sambani Constantina; La Starza Roberta; Pierini Valentina; Vandenberghe Peter; Gonzales-Aguilera Juan J; Rigana Helen; Koumbi Daphne; Manola Kalliopi N; Stavropoulou Chryssa; Georgakakos Vasileios N; Pagoni Maria; Wlodarska Iwona; Mecucci Cristina
Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9).
Cancer genetics and cytogenetics 2005;162(1):45-9.
2005: Quentmeier H; Martelli M P; Dirks W G; Bolli N; Liso A; Macleod R A F; Nicoletti I; Mannucci R; Pucciarini A; Bigerna B; Martelli M F; Mecucci C; Drexler H G; Falini B
Cell line OCI/AML3 bears exon-12 NPM gene mutation-A and cytoplasmic expression of nucleophosmin.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2005;19(10):1760-7.
2005: La Starza R; Aventin A; Crescenzi B; Gorello P; Specchia G; Cuneo A; Angioni A; Bilhou-Nabera C; Boqué C; Foà R; Uyttebroeck A; Talmant P; Cimino G; Martelli M F; Marynen P; Mecucci C; Hagemeijer A
CIZ gene rearrangements in acute leukemia: report of a diagnostic FISH assay and clinical features of nine patients.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2005;19(9):1696-9.
2005: Roti Giovanni; La Starza Roberta; Gorello Paolo; Gottardi Enrico; Crescenzi Barbara; Martelli Massimo F; Mecucci Cristina
e6a2 BCR/ABL1 fusion with cryptic der(9)t(9;22) deletions in a patient with chronic myeloid leukemia.
Haematologica 2005;90(8):1139-41.
2005: Noguera N I; Ammatuna E; Zangrilli D; Lavorgna S; Divona M; Buccisano F; Amadori S; Mecucci C; Falini B; Lo-Coco F
Simultaneous detection of NPM1 and FLT3-ITD mutations by capillary electrophoresis in acute myeloid leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2005;19(8):1479-82.
2005: Cazzaniga Giovanni; Dell'Oro Maria Grazia; Mecucci Cristina; Giarin Emanuela; Masetti Riccardo; Rossi Vincenzo; Locatelli Franco; Martelli Massimo F; Basso Giuseppe; Pession Andrea; Biondi Andrea; Falini Brunangelo
Nucleophosmin mutations in childhood acute myelogenous leukemia with normal karyotype.
Blood 2005;106(4):1419-22.
2005: Alcalay Myriam; Tiacci Enrico; Bergomas Roberta; Bigerna Barbara; Venturini Elisa; Minardi Simone P; Meani Natalia; Diverio Daniela; Bernard Loris; Tizzoni Laura; Volorio Sara; Luzi Lucilla; Colombo Emanuela; Lo Coco Francesco; Mecucci Cristina; Falini Brunangelo; Pelicci Pier Giuseppe
Acute myeloid leukemia bearing cytoplasmic nucleophosmin (NPMc+ AML) shows a distinct gene expression profile characterized by up-regulation of genes involved in stem-cell maintenance.
Blood 2005;106(3):899-902.
2005: La Starza Roberta; Specchia Giorgina; Cuneo Antonio; Beacci Donatella; Nozzoli Chiara; Luciano Luigiana; Aventin Anna; Sambani Constantina; Testoni Nicoletta; Foppoli Marco; Invernizzi Rosangela; Marynen Peter; Martelli Massimo F; Mecucci Cristina
The hypereosinophilic syndrome: fluorescence in situ hybridization detects the del(4)(q12)-FIP1L1/PDGFRA but not genomic rearrangements of other tyrosine kinases.
Haematologica 2005;90(5):596-601.
2005: Aversa Franco; Terenzi Adelmo; Tabilio Antonio; Falzetti Franca; Carotti Alessandra; Ballanti Stelvio; Felicini Rita; Falcinelli Flavio; Velardi Andrea; Ruggeri Loredana; Aloisi Teresa; Saab Jean Pierre; Santucci Antonella; Perruccio Katia; Martelli Maria Paola; Mecucci Cristina; Reisner Yair; Martelli Massimo F
Full haplotype-mismatched hematopoietic stem-cell transplantation: a phase II study in patients with acute leukemia at high risk of relapse.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2005;23(15):3447-54.
2005: Corveleyn Anniek; Wlodarska Iwona; Mecucci Cristina; Marynen Peter
The der(12)t(12;16) breakpoint in an acute leukaemia case targets a Sec7 domain containing protein.
International journal of oncology 2005;26(4):1111-20.
2005: Falini Brunangelo; Mecucci Cristina; Tiacci Enrico; Alcalay Myriam; Rosati Roberto; Pasqualucci Laura; La Starza Roberta; Diverio Daniela; Colombo Emanuela; Santucci Antonella; Bigerna Barbara; Pacini Roberta; Pucciarini Alessandra; Liso Arcangelo; Vignetti Marco; Fazi Paola; Meani Natalia; Pettirossi Valentina; Saglio Giuseppe; Mandelli Franco; Lo-Coco Francesco; Pelicci Pier-Giuseppe; Martelli Massimo F;
Cytoplasmic nucleophosmin in acute myelogenous leukemia with a normal karyotype.
The New England journal of medicine 2005;352(3):254-66.
2004: Rotoli Bruno; Catalano Lucio; Galderisi Maurizio; Luciano Luigia; Pollio Giuditta; Guerriero Anna; D'Errico Arcangelo; Mecucci Cristina; La Starza Roberta; Frigeri Ferdinando; Di Francia Raffaele; Pinto Antonio
Rapid reversion of Loeffler's endocarditis by imatinib in early stage clonal hypereosinophilic syndrome.
Leukemia & lymphoma 2004;45(12):2503-7.
2004: La Starza Roberta; Gorello Paolo; Rosati Roberto; Riezzo Antonio; Veronese Angelo; Ferrazzi Eros; Martelli Massimo F; Negrini Massimo; Mecucci Cristina
Cryptic insertion producing two NUP98/NSD1 chimeric transcripts in adult refractory anemia with an excess of blasts.
Genes, chromosomes & cancer 2004;41(4):395-9.
2004: Malcovati Luca; La Starza Roberta; Merante Serena; Pietra Daniela; Mecucci Cristina; Cazzola Mario
Hypereosinophilic syndrome and cyclic oscillations in blood cell counts. A clonal disorder of hematopoiesis originating in a pluripotent stem cell.
Haematologica 2004;89(4):497-9.
2004: Sambani Constantina; La Starza Roberta; Roumier Christophe; Crescenzi Barbara; Stavropoulou Chryssa; Katsarou Olga; Karafoulidou Anastasia; Dhalle Jean Hugues; Lai Jean-Luc; Preudhomme Claude; Martelli Massimo Fabrizio; Mecucci Cristina
Partial duplication of the MLL oncogene in patients with aggressive acute myeloid leukemia.
Haematologica 2004;89(4):403-7.
2004: Crescenzi Barbara; La Starza Roberta; Romoli Silvia; Beacci Donatella; Matteucci Caterina; Barba Gianluca; Aventin Ana; Marynen Peter; Ciolli Stefania; Nozzoli Chiara; Martelli Massimo Fabrizio; Mecucci Cristina
Submicroscopic deletions in 5q- associated malignancies.
Haematologica 2004;89(3):281-5.
2003: Fiorilli Massimo; Mecucci Cristina; Farci Patrizia; Casato Milvia
HCV-associated lymphomas.
Reviews in clinical and experimental hematology 2003;7(4):406-23.
2003: Cimino Giuseppe; Elia Loredana; Mancini Marco; Annino Luciana; Anaclerico Barbara; Fazi Paola; Vitale Antonella; Specchia Giorgina; Di Raimondo Francesco; Recchia Anna; Cuneo Antonio; Mecucci Cristina; Pane Fabrizio; Saglio Giuseppe; Foa Robin; Mandelli Franco;
Clinico-biologic features and treatment outcome of adult pro-B-ALL patients enrolled in the GIMEMA 0496 study: absence of the ALL1/AF4 and of the BCR/ABL fusion genes correlates with a significantly better clinical outcome.
Blood 2003;102(6):2014-20.
2003: Matteucci Caterina; Galieni Piero; Leoncini Lorenzo; Lazzi Stefano; Lauria Francesco; Polito Ennio; Martelli Massimo F; Mecucci Cristina
Typical genomic imbalances in primary MALT lymphoma of the orbit.
The Journal of pathology 2003;200(5):656-60.
2003: Barozzi Patrizia; Luppi Mario; Facchetti Fabio; Mecucci Cristina; Alù Milena; Sarid Ronit; Rasini Valeria; Ravazzini Luisa; Rossi Elisa; Festa Silvana; Crescenzi Barbara; Wolf Dana G; Schulz Thomas F; Torelli Giuseppe
Post-transplant Kaposi sarcoma originates from the seeding of donor-derived progenitors.
Nature medicine 2003;9(5):554-61.
2003: La Starza Roberta; Trubia Maurizio; Crescenzi Barbara; Matteucci Caterina; Negrini Massimo; Martelli Massimo F; Pelicci Pier Giuseppe; Mecucci Cristina
Human homeobox gene HOXC13 is the partner of NUP98 in adult acute myeloid leukemia with t(11;12)(p15;q13).
Genes, chromosomes & cancer 2003;36(4):420-3.
2003: Foa Robin; Vitale Antonella; Mancini Marco; Cuneo Antonio; Mecucci Cristina; Elia Loredana; Lombardo Romina; Saglio Giuseppe; Torelli Giuseppe; Annino Luciana; Specchia Giorgina; Damasio Eugenio; Recchia Anna; Di Raimondo Francesco; Morra Enrica; Volpe Ettore; Tafuri Agostino; Fazi Paola; Hunger Stephen P; Mandelli Franco
E2A-PBX1 fusion in adult acute lymphoblastic leukaemia: biological and clinical features.
British journal of haematology 2003;120(3):484-7.
2003: Matteucci Caterina; La Starza Roberta; Crescenzi Barbara; Romoli Silvia; Santoro Alessandra; Magrin Silvana; Lauria Francesco; Coco Francesco Lo; Martelli Massimo F; Mecucci Cristina
Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia.
Cancer genetics and cytogenetics 2003;140(1):13-7.
2002: Agnello Vincent; Mecucci Cristina; Casato Milvia
Regression of splenic lymphoma after treatment of hepatitis C virus infection.
The New England journal of medicine 2002;347(26):2168-70; author reply 2168-70.
2002: Martini Alessandra; La Starza Roberta; Janssen Hilde; Bilhou-Nabera Chrystèle; Corveleyn Anniek; Somers Riet; Aventin Ana; Foà Robin; Hagemeijer Anne; Mecucci Christina; Marynen Peter
Recurrent rearrangement of the Ewing's sarcoma gene, EWSR1, or its homologue, TAF15, with the transcription factor CIZ/NMP4 in acute leukemia.
Cancer research 2002;62(19):5408-12.
2002: Mancini M; Vegna M L; Castoldi G L; Mecucci C; Spirito F; Elia L; Tafuri A; Annino L; Pane F; Rege-Cambrin G; Gottardi M; Leoni P; Gallo E; Camera A; Luciano L; Specchia G; Torelli G; Sborgia M; Gabbas A; Tedeschi A; Della Starza I; Cascavilla N; Di Raimondo F; Mandelli F; Foà R
Partial deletions of long arm of chromosome 6: biologic and clinical implications in adult acute lymphoblastic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2002;16(10):2055-61.
2002: Cuneo A; Bigoni R; Cavazzini F; Bardi A; Roberti M G; Agostini P; Tammiso E; Ciccone N; Mancini M; Nanni M; De Cuia R; Divona M; La Starza R; Crescenzi B; Testoni N; Rege Cambrin G; Mecucci C; Lo Coco F; Saglio G; Castoldi G
Incidence and significance of cryptic chromosome aberrations detected by fluorescence in situ hybridization in acute myeloid leukemia with normal karyotype.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2002;16(9):1745-51.
2002: La Starza Roberta; Trubia Maurizio; Testoni Nicoletta; Ottaviani Emanuela; Belloni Elena; Crescenzi Barbara; Martelli Massimo; Flandrin Georges; Pelicci Pier Giuseppe; Mecucci Cristina
Clonal eosinophils are a morphologic hallmark of ETV6/ABL1 positive acute myeloid leukemia.
Haematologica 2002;87(8):789-94.
2002: Tafuri Agostino; Gregorj Chiara; Petrucci Maria T; Ricciardi Maria R; Mancini Marco; Cimino Giuseppe; Mecucci Cristina; Tedeschi Alessandra; Fioritoni Giuseppe; Ferrara Felicetto; Di Raimondo Francesco; Gallo Eugenio; Liso Vincenzo; Fabbiano Francesco; Cascavilla Nicola; Pizzolo Giovanni; Camera Andrea; Pane Fabrizio; Lanza Francesco; Cilloni Daniela; Annino Luciana; Vitale Antonella; Vegna Maria L; Vignetti Marco; Foà Robin; Mandelli Franco;
MDR1 protein expression is an independent predictor of complete remission in newly diagnosed adult acute lymphoblastic leukemia.
Blood 2002;100(3):974-81.
2002: Matteucci Caterina; La Starza Roberta; Crescenzi Barbara; Falzetti Daniela; Romoli Silvia; Emiliani Carla; Orlacchio Aldo; Marynen Peter; Martelli Massimo F; Mecucci Cristina
Interpretation of the complex karyotype and identification of a new 6p amplicon by integrated comparative genomic hybridization and fluorescence in situ hybridization on the U937-I cell line.
Cancer genetics and cytogenetics 2002;135(1):28-34.
2002: Crescenzi B; Sacchi S; Marasca R; Temperani P; La Starza R; Matteucci C; Bonacorsi G; Romoli S; Martelli M F; Mecucci C; Emilia G
Distinct genomic events in the myeloid and lymphoid lineages in simultaneous presentation of chronic myeloid leukemia and B-chronic lymphocytic leukemia.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2002;16(5):955-6.
2002: Rosati Roberto; La Starza Roberta; Veronese Angelo; Aventin Ana; Schwienbacher Christine; Vallespi Teresa; Negrini Massimo; Martelli Massimo F; Mecucci Cristina
NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15).
Blood 2002;99(10):3857-60.
2002: Mecucci Cristina; Rosati Roberto; Starza Roberta La
Genetic profile of acute myeloid leukemia.
Reviews in clinical and experimental hematology 2002;6(1):3-25; discussion 86-7.
2002: Casato Milvia; Mecucci Cristina; Agnello Vincent; Fiorilli Massimo; Knight Glenn B; Matteucci Caterina; Gao Lei; Kay Jonathan
Regression of lymphoproliferative disorder after treatment for hepatitis C virus infection in a patient with partial trisomy 3, Bcl-2 overexpression, and type II cryoglobulinemia.
Blood 2002;99(6):2259-61.
2002: Sambani Constantina; La Starza Roberta; Stavropoulou Chryssa; Manola Kalliopi N; Harhalakis Nicholas; Mecucci Cristina
A novel dic(1;10) in a patient with myelodysplastic syndrome.
Cancer genetics and cytogenetics 2002;133(1):87-9.
2002: La Starza Roberta; Testoni Nicoletta; Lafage-Pochitaloff Marina; Ruggeri Deborah; Ottaviani Emanuela; Perla Gianni; Martelli Massimo Fabrizio; Marynen Peter; Mecucci Cristina
Complex variant Philadelphia translocations involving the short arm of chromosome 6 in chronic myeloid leukemia.
Haematologica 2002;87(2):143-7.
2002: La Starza Roberta; Vitale Antonella; Serra Anna; Saglio Giuseppe; Fioritoni Giuseppe; Falzetti Daniela; Martelli Massimo F; Foà Robin; Mecucci Cristina
Philadelphia-positive acute lymphoblastic leukemia with multiple subclones including duplication of the Philadelphia chromosome and Abelson oncogene.
Cancer genetics and cytogenetics 2002;132(1):46-50.
2001: Sambani C; Trafalis D T; Mitsoulis-Mentzikoff C; Poulakidas E; Makropoulos V; Pantelias G E; Mecucci C
Clonal chromosome rearrangements in hairy cell leukemia: personal experience and review of literature.
Cancer genetics and cytogenetics 2001;129(2):138-44.
2001: Visani G; Bernasconi P; Boni M; Castoldi G L; Ciolli S; Clavio M; Cox M C; Cuneo A; Del Poeta G; Dini D; Falzetti D; Fanin R; Gobbi M; Isidori A; Leoni F; Liso V; Malagola M; Martinelli G; Mecucci C; Piccaluga P P; Petti M C; Rondelli R; Russo D; Sessarego M; Specchia G; Testoni N; Torelli G; Mandelli F; Tura S
The prognostic value of cytogenetics is reinforced by the kind of induction/consolidation therapy in influencing the outcome of acute myeloid leukemia--analysis of 848 patients.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2001;15(6):903-9.
2001: Ascoli V; Aalto Y; Carnovale-Scalzo C; Nardi F; Falzetti D; Mecucci C; Knuutila S
DNA copy number changes in familial malignant mesothelioma.
Cancer genetics and cytogenetics 2001;127(1):80-2.
2001: La Starza R; Aventin A; Falzetti D; Wlodarska I; Fernandez Peralta A M; Gonzalez-Aguilera J J; Ciolli S; Martelli M F; Mecucci C
Regions of juxtaposition in unbalanced 1q rearrangements of malignant hemopathies.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2001;15(5):861-3.
2001: Cimino G; Sprovieri T; Rapanotti M C; Foà R; Mecucci C; Mandelli F
Molecular evaluation of the NUP98/RAP1GDS1 gene frequency in adults with T-acute lymphoblastic leukemia.
Haematologica 2001;86(4):436-7.
2001: La Starza R; Sambani C; Crescenzi B; Matteucci C; Martelli M F; Mecucci C
AML1/MTG16 fusion gene from a t(16;21)(q24;q22) translocation in treatment-induced leukemia after breast cancer.
Haematologica 2001;86(2):212-3.
2001: Mancini M; Nanni M; Sirleto P; De Cuia M R; Castoldi G L; Cilloni D; Cimino G; Mecucci C; Pane F; Annino L; Di Raimondo F; Santoro A; Specchia G; Tedeschi A; Todeschini G; Foá R;
Detection of BCR/ABL rearrangements in adult acute lymphoblastic leukemia using a highly sensitive interphase fluorescence in situ hybridization method (D-FISH).
The hematology journal : the official journal of the European Haematology Association / EHA 2001;2(1):54-60.
2000: Spirito F R; Crescenzi B; Matteucci C; Martelli M F; Mecucci C
Cytogenetic characterization of acute myeloid leukemia in Shwachman's syndrome. A case report.
Haematologica 2000;85(11):1207-10.
2000: Crescenzi B; Fizzotti M; Piattoni S; La Starza R; Matteucci C; Carotti A; Aversa F; Martelli M F; Mecucci C
Interphase FISH for Y chromosome, VNTR polymorphisms, and RT-PCR for BCR-ABL in the monitoring of HLA-matched and mismatched transplants.
Cancer genetics and cytogenetics 2000;120(1):25-9.
2000: Mecucci C; La Starza R; Negrini M; Sabbioni S; Crescenzi B; Leoni P; Di Raimondo F; Krampera M; Cimino G; Tafuri A; Cuneo A; Vitale A; Foà R
t(4;11)(q21;p15) translocation involving NUP98 and RAP1GDS1 genes: characterization of a new subset of T acute lymphoblastic leukaemia.
British journal of haematology 2000;109(4):788-93.
2000: Falzetti D; Vermeesch J R; Matteucci C; Ciolli S; Martelli M F; Marynen P; Mecucci C
Microdissection and FISH investigations in acute myeloid leukemia: a step forward to full identification of complex karyotypic changes.
Cancer genetics and cytogenetics 2000;118(1):28-34.
2000: Mancini M; Cedrone M; Diverio D; Emanuel B; Stul M; Vranckx H; Brama M; De Cuia M R; Nanni M; Fazi F; Mecucci C; Alimena G; Hagemeijer A
Use of dual-color interphase FISH for the detection of inv(16) in acute myeloid leukemia at diagnosis, relapse and during follow-up: a study of 23 patients.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2000;14(3):364-8.
2000: Cimino G; Elia L; Rapanotti M C; Sprovieri T; Mancini M; Cuneo A; Mecucci C; Fioritoni G; Carotenuto M; Morra E; Liso V; Annino L; Saglio G; De Rossi G; Foà R; Mandelli F
A prospective study of residual-disease monitoring of the ALL1/AF4 transcript in patients with t(4;11) acute lymphoblastic leukemia.
Blood 2000;95(1):96-101.
1999: La Starza R; Stella M; Testoni N; Di Bona E; Ciolli S; Marynen P; Martelli M F; Mandelli F; Mecucci C
Characterization of 12p molecular events outside ETV6 in complex karyotypes of acute myeloid malignancies.
British journal of haematology 1999;107(2):340-6.
1999: Mecucci C; Falzetti D; La Starza R
Metaphase FISH, microdissection, and multicolour FISH. Applications in haematology.
Haematologica 1999;84 Suppl EHA-4():98-101.
1999: Falzetti D; Vermeesch J R; Hood T L; Nacheva E P; Matteucci C; Martelli M F; Van den Berghe H; Marynen P; Mecucci C
Identification of multiple copies of a 20q-chromosome in a case of myelodysplastic syndrome: a FISH study.
Leukemia research 1999;23(4):407-13.
1999: Falzetti D; Crescenzi B; Matteuci C; Falini B; Martelli M F; Van Den Berghe H; Mecucci C
Genomic instability and recurrent breakpoints are main cytogenetic findings in Hodgkin's disease.
Haematologica 1999;84(4):298-305.
1999: Wlodarska I; Selleri L; La Starza R; Paternotte C; Evans G A; Boogaerts M; Van den Berghe H; Mecucci C
Molecular cytogenetics localizes two new breakpoints on 11q23.3 and 21q11.2 in myelodysplastic syndrome with t(11;21) translocation.
Genes, chromosomes & cancer 1999;24(3):199-206.
1999: Mecucci C; La Starza R
Cytogenetics of myelodysplastic syndromes.
Forum (Genoa, Italy) 1999;9(1):4-13.
1999: Aventín A; La Starza R; Martínez C; Wlodarska I; Boogaerts M; Van den Berghe H; Mecucci C
Involvement of MLL gene in a t(10;11)(q22;q23) and a t(8;11)(q24;q23) identified by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1999;108(1):48-52.
1999: Cools J; Peeters P; Voet T; Aventin A; Mecucci C; Grandchamp B; Marynen P
Genomic organization of human JAK2 and mutation analysis of its JH2-domain in leukemia.
Cytogenetics and cell genetics 1999;85(3-4):260-6.
1998: Angioni A; La Starza R; Mecucci C; Sprovieri T; Matteucci C; De Rossi G; Balloni P; Cimino G
Interstitial insertion of AF10 into the ALL1 gene in a case of infant acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1998;107(2):107-10.
1998: La Starza R; Wlodarska I; Matteucci C; Falzetti D; Baens M; Martelli M F; Van den Berghe H; Marynen P; Mecucci C
Rearrangement between the MYH11 gene at 16p13 and D12S158 at 12p13 in a case of acute myeloid leukemia M1 (AML-M1).
Genes, chromosomes & cancer 1998;23(1):10-5.
1998: La Starza R; Matteucci C; Crescenzi B; Criel A; Selleslag D; Martelli M F; Van den Berghe H; Mecucci C
Trisomy 6 is the hallmark of a dysplastic clone in bone marrow aplasia.
Cancer genetics and cytogenetics 1998;105(1):55-9.
1998: Mecucci C
Molecular features of primary MDS with cytogenetic changes.
Leukemia research 1998;22(4):293-302.
1998: Wlodarska I; La Starza R; Baens M; Dierlamm J; Uyttebroeck A; Selleslag D; Francine A; Mecucci C; Hagemeijer A; Van den Berghe H; Marynen P
Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignancies.
Blood 1998;91(4):1399-406.
1998: Cuneo A; Bigoni R; Roberti M G; Bardi A; Rigolin G M; Piva N; Mancini M; Nanni M; Alimena G; Mecucci C; Matteucci C; La Starza R; Bernasconi P; Cavigliano P; Genini E; Zaccaria A; Testoni N; Carboni C; Castoldi G
Detection and monitoring of trisomy 8 by fluorescence in situ hybridization in acute myeloid leukemia: a multicentric study.
Haematologica 1998;83(1):21-6.
1998: La Starza R; Wlodarska I; Aventin A; Falzetti D; Crescenzi B; Martelli M F; Van den Berghe H; Mecucci C
Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies.
Blood 1998;91(1):231-7.
1997: Dierlamm J; Wlodarska I; Michaux L; Vermeesch J R; Meeus P; Stul M; Criel A; Verhoef G; Thomas J; Delannoy A; Louwagie A; Cassiman J J; Mecucci C; Hagemeijer A; Van den Berghe H
FISH identifies different types of duplications with 12q13-15 as the commonly involved segment in B-cell lymphoproliferative malignancies characterized by partial trisomy 12.
Genes, chromosomes & cancer 1997;20(2):155-66.
1997: Wlodarska I; Pittaluga S; Stul M; Martiat P; Dierlamm J; Michaux L; De Wolf-Peeters C; Cassiman J J; Mecucci C; Van den Berghe H
Philadelphia-like translocation t(9;22)(q34;q11) found in a follicular lymphoma involving not BCR and ABL but IGL-mediated rearrangement of an unknown gene on 9q34.
Genes, chromosomes & cancer 1997;20(2):113-9.
1997: Starza R L; Matteucci C; Crescenzi B; Perla G; Carotenuto M; Martelli M F; Hagemeijer A; Mecucci C
Identification of chromosome changes in acute myeloid leukemia (AML-M2) by molecular cytogenetics.
Cancer genetics and cytogenetics 1997;95(2):148-52.
1997: Criel A; Verhoef G; Vlietinck R; Mecucci C; Billiet J; Michaux L; Meeus P; Louwagie A; Van Orshoven A; Van Hoof A; Boogaerts M; Van den Berghe H; De Wolf-Peeters C
Further characterization of morphologically defined typical and atypical CLL: a clinical, immunophenotypic, cytogenetic and prognostic study on 390 cases.
British journal of haematology 1997;97(2):383-91.
1997: Wlodarska I; Aventín A; Inglés-Esteve J; Falzetti D; Criel A; Cassiman J J; Mecucci C; Van den Berghe H; Marynen P
A new subtype of pre-B acute lymphoblastic leukemia with t(5;12)(q31q33;p12), molecularly and cytogenetically distinct from t(5;12) in chronic myelomonocytic leukemia.
Blood 1997;89(5):1716-22.
1997: Hernandez J M; Mecucci C; Michaux L; Criel A; Stul M; Meeus P; Wlodarska I; Van Orshoven A; Cassiman J J; De Wolf-Peeters C; Van den Berghe H
del(7q) in chronic B-cell lymphoid malignancies.
Cancer genetics and cytogenetics 1997;93(2):147-51.
1997: Ascoli V; Lo Coco F; Artini M; Levrero M; Fruscalzo A; Mecucci C
Primary effusion Burkitt's lymphoma with t(8;22) in a patient with hepatitis C virus-related cirrhosis.
Human pathology 1997;28(1):101-4.
1996: Wlodarska I; Mecucci C; Baens M; Marynen P; van den Berghe H
ETV6 gene rearrangements in hematopoietic malignant disorders.
Leukemia & lymphoma 1996;23(3-4):287-95.
1996: Dierlamm J; Wlodarska I; Michaux L; La Starza R; Zeller W; Mecucci C; Van den Berghe H
Successful use of the same slide for consecutive fluorescence in situ hybridization experiments.
Genes, chromosomes & cancer 1996;16(4):261-4.
1996: Dierlamm J; Michaux L; Kröger N; Wlodarska I; Martiat P; Zeller W; Seeger D; Mecucci C; van den Berghe H; Hossfeld D K
ider(9)(q10)t(9;22)(q34;q11) is a recurrent chromosomal abnormality in acute lymphoblastic leukemia and lymphatic blastic phase of chronic myelogenous leukemia.
Cancer genetics and cytogenetics 1996;89(2):109-13.
1996: Pittaluga S; Ayoubi T A; Wlodarska I; Stul M; Cassiman J J; Mecucci C; Van Den Berghe H; Van De Ven W J; De Wolf-Peeters C
BCL-6 expression in reactive lymphoid tissue and in B-cell non-Hodgkin's lymphomas.
The Journal of pathology 1996;179(2):145-50.
1996: Wlodarska I; Baens M; Peeters P; Aerssens J; Mecucci C; Brock P; Marynen P; Van den Berghe H
Biallelic alterations of both ETV6 and CDKN1B genes in a t(12;21) childhood acute lymphoblastic leukemia case.
Cancer research 1996;56(11):2655-61.
1996: Criel A; Pittaluga S; Verhoef G; Wlodarska I; Meeus P; Mecucci C; Van Orshoven A; Van den Berghe H; Boogaerts M; De Wolf-Peeters C
Small B cell NHL and their leukemic counterpart: differences in subtyping and assessment of leukemic spread.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1996;10(5):848-53.
1996: Michaux L; Dierlamm J; Mecucci C; Meeus P; Ameye G; Libouton J M; Verhoef G; Ferrant A; Louwagie A; Verellen-Dumoulin C; Van Den Berghe H
Dicentric (1;15) in myeloid disorders.
Cancer genetics and cytogenetics 1996;88(1):86-9.
1996: Dierlamm J; Michaux L; Wlodarska I; Pittaluga S; Zeller W; Stul M; Criel A; Thomas J; Boogaerts M; Delaere P; Cassiman J J; de Wolf-Peeters C; Mecucci C; Van den Berghe H
Trisomy 3 in marginal zone B-cell lymphoma: a study based on cytogenetic analysis and fluorescence in situ hybridization.
British journal of haematology 1996;93(1):242-9.
1996: Velloso E R; Mecucci C; Michaux L; Van Orshoven A; Stul M; Boogaerts M; Bosly A; Cassiman J J; Van Den Berghe H
Translocation t(8;16)(p11;p13) in acute non-lymphocytic leukemia: report on two new cases and review of the literature.
Leukemia & lymphoma 1996;21(1-2):137-42.
1996: Velloso E R; Michaux L; Ferrant A; Hernandez J M; Meeus P; Dierlamm J; Criel A; Louwagie A; Verhoef G; Boogaerts M; Michaux J L; Bosly A; Mecucci C; Van den Berghe H
Deletions of the long arm of chromosome 7 in myeloid disorders: loss of band 7q32 implies worst prognosis.
British journal of haematology 1996;92(3):574-81.
1996: La Starza R; Aventin A; Falzetti D; Stul M; Martelli M F; Falini B; Mecucci C
14q+ chromosome marker in a T-cell-rich B-cell lymphoma.
The Journal of pathology 1996;178(2):227-31.
1996: Michaux L; Mecucci C; Pereira Velloso E R; Dierlamm J; Criel A; Louwagie A; van Orshoven A; van den Berghe H
About the t(8;13)(p11;q12) clinico-pathologic entity.
Blood 1996;87(4):1658-9.
1996: Pittaluga S; Verhoef G; Criel A; Wlodarska I; Dierlamm J; Mecucci C; Van den Berghe H; De Wolf-Peeters C
"Small" B-cell non-Hodgkin's lymphomas with splenomegaly at presentation are either mantle cell lymphoma or marginal zone cell lymphoma. A study based on histology, cytology, immunohistochemistry, and cytogenetic analysis.
The American journal of surgical pathology 1996;20(2):211-23.
1996: Michaux L; Mecucci C; Stul M; Wlodarska I; Hernandez J M; Meeus P; Michaux J L; Scheiff J M; Noël H; Louwagie A; Criel A; Boogaerts M; Van Orshoven A; Cassiman J J; Van Den Berghe H
BCL3 rearrangement and t(14;19)(q32;q13) in lymphoproliferative disorders.
Genes, chromosomes & cancer 1996;15(1):38-47.
1996: Michaux L; Wlodarska I; Vellosa E R; Verhoef G; Van Orshoven A; Michaux J L; Scheiff J M; Mecucci C; Van den Berghe H
Translocation (Y;1)(q12;q12) in hematologic malignancies. Report on two new cases, FISH characterization, and review of the literature.
Cancer genetics and cytogenetics 1996;86(1):35-8.
1996: Dierlamm J; Pittaluga S; Wlodarska I; Stul M; Thomas J; Boogaerts M; Michaux L; Driessen A; Mecucci C; Cassiman J J; De Wolf-Peeters C; Van den Berghe H
Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features.
Blood 1996;87(1):299-307.
1996: Wlodarska I; Marynen P; La Starza R; Mecucci C; Van den Berghe H
The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberration in different hematological malignancies.
Cytogenetics and cell genetics 1996;72(2-3):229-35.
1995: Hernandez J M; Mecucci C; Criel A; Meeus P; Michaux I; Van Hoof A; Verhoef G; Louwagie A; Scheiff J M; Michaux J L
Cytogenetic analysis of B cell chronic lymphoid leukemias classified according to morphologic and immunophenotypic (FAB) criteria.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(12):2140-6.
1995: Dierlamm J; Michaux L; Criel A; Wlodarska I; Zeller W; Louwagie A; Michaux J L; Mecucci C; Van den Berghe H
Isodicentric (X)(q13) in haematological malignancies: presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literature.
British journal of haematology 1995;91(4):885-91.
1995: Michaux L; Dierlamm J; Wlodarska I; Stul M; Bosly A; Delannoy A; Louwagie A; Mecucci C; Cassiman J J; van den Berghe H
Trisomy 3 is a consistent chromosome change in malignant lymphoproliferative disorders preceded by cold agglutinin disease.
British journal of haematology 1995;91(2):421-4.
1995: Wlodarska I; De Wolf-Peeters C; Michaux L; Mecucci C; Verhoef G; Cassiman J J; Van den Berghe H
A new t(2;5) translocation in a null cell type CD30 positive anaplastic large cell lymphoma case.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(10):1685-8.
1995: Wlodarska I; Mecucci C; Stul M; Michaux L; Pittaluga S; Hernandez J M; Cassiman J J; De Wolf-Peeters C; Van den Berghe H
Fluorescence in situ hybridization identifies new chromosomal changes involving 3q27 in non-Hodgkin's lymphomas with BCL6/LAZ3 rearrangement.
Genes, chromosomes & cancer 1995;14(1):1-7.
1995: Meeus P; Stul M S; Mecucci C; Cassiman J J; Van den Berghe H
Molecular breakpoints of t(11;14)(q13;q32) in multiple myeloma.
Cancer genetics and cytogenetics 1995;83(1):25-7.
1995: Hernández J M; Mecucci C; Beverloo H B; Selleri L; Wlodarska I; Stul M; Michaux L; Verhoef G; Van Orshoven A; Cassiman J J
Translocation (11;15)(q23;q14) in three patients with acute non-lymphoblastic leukemia (ANLL): clinical, cytogenetic and molecular studies.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1995;9(7):1162-6.
1995: Criel A; Mecucci C; Wlodarska I; Meeus P; Stul M; Cassiman J J; Louwagie A; Van Hoof A; Hidajat M; Van den Berghe H
Trisomy 12 does not correlate with EBV infection in chronic B-cell leukemias.
Cancer genetics and cytogenetics 1995;82(1):80-1.
1995: Michaux L; Wlodarska I; Mecucci C; Hernandez J M; Van Orshoven A; Michaux J L; Van den Berghe H
Characterization by chromosome painting of balanced and unbalanced X chromosome translocations in myelodysplastic syndromes.
Cancer genetics and cytogenetics 1995;82(1):17-22.
1995: Wlodarska I; Mecucci C; Marynen P; Guo C; Franckx D; La Starza R; Aventin A; Bosly A; Martelli M F; Cassiman J J
TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13).
Blood 1995;85(10):2848-52.
1995: La Starza R; Crescenzi B; Matteucci C; Martelli M F; Mecucci C
Cytogenetic and FISH investigations on tetrasomy 8 in ANLL.
Cancer genetics and cytogenetics 1995;79(2):182-5.
1994: Aventín A; Espadaler M; Martín-Henao G A; Mecucci C
Isochromosome 17q- in acute promyelocytic leukemia. Molecular characterization by fluorescence in situ hybridization.
Cancer genetics and cytogenetics 1994;78(1):112-3.
1994: Wlodarska I; Mecucci C; De Wolf-Peeters C; Verhoef G; Weier H U; Cassiman J J; Van Den Berghe H
"Jumping" translocation of 9q in a case of follicular lymphoma.
Cancer genetics and cytogenetics 1994;76(2):140-4.
1994: Criel A; Wlodarska I; Meeus P; Stul M; Louwagie A; Van Hoof A; Hidajat M; Mecucci C; Van den Berghe H
Trisomy 12 is uncommon in typical chronic lymphocytic leukaemias.
British journal of haematology 1994;87(3):523-8.
1994: La Starza R; Falzetti D; Fania C; Tabilio A; Martelli M F; Mecucci C
3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus.
Haematologica 1994;79(4):356-9.
1994: Wlodarska I; Stul M; De Wolf-Peeters C; Verhoef G; Mecucci C; Cassiman J J; Van den Berghe H
t(1;19) without detectable E2A rearrangements in two t(14;18)-positive lymphoma/leukemia cases.
Genes, chromosomes & cancer 1994;10(3):171-6.
1994: Angioni A; Ruscio C; Giovannelli L; Miano C; Rosati D; Balloni P; De Laurenzi A; Mecucci C
Characterization of a new case of trisomy 8 in acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1994;74(2):144-6.
1994: Wlodarska I; De Wolf-Peeters C; Dierick H; Hilliker C; Thomas J; Mecucci C; Cassiman J J; Van den Berghe H
Detection of amplified sequences at 5q11-->q13 in a homogenously staining region found by fluorescent in situ hybridization in a case of B-cell non-Hodgkin's lymphoma.
Cytogenetics and cell genetics 1994;65(3):179-83.
1994: Mecucci C; van den Berghe H
Cytogenetics and immunophenotype.
Leukemia & lymphoma 1994;13 Suppl 1():49-51.
1993: Stul M; Baens M; Mecucci C; Van den Berghe H; Cassiman J J
Rare HRAS1 alleles outside the VTR region in lymph nodes from patients with malignant lymphoma.
Cancer genetics and cytogenetics 1993;69(1):60-4.
1993: Wlodarska I; Delabie J; De Wolf-Peeters C; Mecucci C; Stul M; Verhoef G; Cassiman J J; Van den Berghe H
T-cell lymphoma developing in Hodgkin's disease: evidence for two clones.
The Journal of pathology 1993;170(3):239-48.
1993: Busschots A M; Geerts M L; Mecucci C; Stul M; Cassiman J J; van den Berghe H
A translocation (8;14) in a cutaneous large B-cell lymphoma.
American journal of clinical pathology 1993;99(5):615-21.
1993: La Starza R; Falini B; Amici A; Falzetti D; Tabilio A; Fagioli M; Martelli M F; Mecucci C
T-lymphoid/myeloid biphenotypic leukemia morphologically resembling malignant histiocytosis. Immunological, cytogenetic and molecular studies.
Haematologica 1993;78(3):187-91.
1992: Vandenberghe E; De Wolf Peeters C; Wlodarska I; Stul M; Louwagie A; Verhoef G; Thomas J; Criel A; Cassiman J J; Mecucci C
Chromosome 11q rearrangements in B non Hodgkin's lymphoma.
British journal of haematology 1992;81(2):212-7.
1992: Wlodarska I; Mecucci C; Vandenberghe E; De Wolf-Peeters C; Thomas J; Hilliker C; Schoenmakers E; Stul M; Marynen P; Cassiman J J
dup(12)(q13----qter) in two t(14;18)-negative follicular B-non-Hodgkin's lymphomas.
Genes, chromosomes & cancer 1992;4(4):302-8.
1992: Mancini M; Mecucci C; Cedrone M; Rondinelli M B; Aloe-Spiriti M A; Alimena G
Unbalanced 6p translocation as primary karyotypic anomaly in secondary acute nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1992;60(1):93-5.
1992: Verhoef G; Meeus P; Stul M; Mecucci C; Cassiman J J; Van Den Berghe H; Boogaerts M
Cytogenetic and molecular studies of the Philadelphia translocation in myelodysplastic syndromes. Report of two cases and review of the literature.
Cancer genetics and cytogenetics 1992;59(2):161-6.
1991: Vandenberghe E; van den Oord J; Mecucci C; Van den Berghe H; De Wolf-Peeters C
B-cell non-Hodgkin's lymphomas of follicle mantle lineage: part of a biological spectrum?
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(10):829-31.
1991: Vandenberghe E; Baens M; Stul M; Bosly A; Cassiman J J; Mecucci C; Van den Berghe H
Alteration of N-ras mutation in a patient with AML M4 and trilineage myelodysplasia.
British journal of haematology 1991;79(2):338-40.
1991: Angioni A; Ghione F; Miano C; Rosati D; Guazzelli C; Balloni P; Mecucci C
Unusual t(3;12)(q28;q13) in childhood acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1991;55(2):261-3.
1991: Walgraeve D; Verhoef G; Stul M; Cassiman J J; Mecucci C; Van den Berghe H; Boogaerts M
Chronic myelogenous leukemia after treatment with 131I for thyroid carcinoma. Report of a case and review of the literature.
Cancer genetics and cytogenetics 1991;55(2):217-24.
1991: Vandenberghe E; Martiat P; Baens M; Stul M; Ferrant A; Cuneo A; Cassiman J J; Mecucci C; Van den Berghe H
Megakaryoblastic leukemia with an N-ras mutation and late acquisition of a Philadelphia chromosome.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1991;5(8):683-6.
1991: Vandenberghe E; de Wolf-Peeters C; Delabie J; Thomas J; Michaux J L; Noël H; Mecucci C; Van Den Berghe H
Cytogenetic characterization of three cases of unusual B-cell non-Hodgkin's lymphoma.
Cancer genetics and cytogenetics 1991;53(2):229-35.
1991: Vandenberghe E; De Wolf-Peeters C; van den Oord J; Wlodarska I; Delabie J; Stul M; Thomas J; Michaux J L; Mecucci C; Cassiman J J
Translocation (11;14): a cytogenetic anomaly associated with B-cell lymphomas of non-follicle centre cell lineage.
The Journal of pathology 1991;163(1):13-8.
1991: Cedrone M; Mecucci C; Burgio V L; Diverio D; Petti M C; Alimena G
Reciprocal translocation involving 3q21 in an unusual myeloproliferative disorder with myelodysplastic features and prominent dysmegakaryopoiesis.
Cancer genetics and cytogenetics 1991;51(1):73-8.
1991: Hillion J; Mecucci C; Aventin A; Leroux D; Wlodarska I; Van Den Berghe H; Larsen C J
A variant translocation t(2;18) in follicular lymphoma involves the 5' end of bcl-2 and Ig kappa light chain gene.
Oncogene 1991;6(1):169-72.
1991: Verhoef G; De Wolf-Peeters C; Kerim S; Van De Broeck J; Mecucci C; Van den Berghe H; Boogaerts M
Update on the prognostic implication of morphology, histology, and karyotype in primary myelodysplastic syndromes.
Hematologic pathology 1991;5(4):163-75.
1990: Verhoef G E; Demuynck H; Stul M S; Cassiman J J; Mecucci C; Van Den Berghe H; Boogaerts M A
Philadelphia chromosome-positive chronic myelogenous leukemia in treated Hodgkin's disease.
Cancer genetics and cytogenetics 1990;49(2):171-6.
1990: Vandenberghe E A; Mecucci C; Delannoy A; Van den Berghe H
Deletion of 5q by t(5;17) in therapy-related myelodysplastic syndrome.
Cancer genetics and cytogenetics 1990;48(1):49-52.
1990: Kerim S; Stul M; Mecucci C; Vandenberghe E; Cuneo A; Dal Cin P; Michaux J L; Louwagie A; Cassiman J J; Van den Berghe H
Rearrangement of immunoglobulin and TCR genes in lymphoid blast crisis of Ph+ chronic myeloid leukaemia.
British journal of haematology 1990;74(4):414-9.
1990: Alimena G; De Cuia M R; Mecucci C; Arcese W; Mauro F; Screnci M; Mancini M; Cedrone M; Nanni M; Montefusco E
Cytogenetic follow-up after allogeneic bone-marrow transplantation for Ph1-positive chronic myelogenous leukemia.
Bone marrow transplantation 1990;5(2):119-27.
1990: Kerim S; Mecucci C; Cuneo A; Vandenberghe E; Louwagie A; Stul M; Michaux J L; Van Den Berghe H
5q- anomaly in lymphoid disorders.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1990;4(1):12-5.
1989: Iurlo A; Mecucci C; Van Orshoven A; Michaux J L; Boogaerts M; Noens L; Bosly A; Louwagie A; Van Den Berghe H
Cytogenetic and clinical investigations in 76 cases with therapy-related leukemia and myelodysplastic syndrome.
Cancer genetics and cytogenetics 1989;43(2):227-41.
1989: Cuneo A; Mecucci C; Kerim S; Vandenberghe E; Dal Cin P; Van Orshoven A; Rodhain J; Bosly A; Michaux J L; Martiat P
Multipotent stem cell involvement in megakaryoblastic leukemia: cytologic and cytogenetic evidence in 15 patients.
Blood 1989;74(5):1781-90.
1989: Aventin A; Mecucci C; Van Orshoven A; Delannoy A; Van den Berghe H
Variant (3;21) translocation and megakaryocytic involvement in blastic crisis of Philadelphia positive chronic myeloid leukaemia.
British journal of haematology 1989;71(4):562-4.
1989: Mecucci C; Van Orshoven A; Boogaerts M; Michaux J L; Van den Berghe H
Characterization of deletions of chromosome 7 short arm occurring as primary karyotypic anomaly in acute myeloid leukaemia.
British journal of haematology 1989;71(1):13-7.
1988: Mecucci C; Delannoy A; Van den Berghe H
The origin of trisomy 12 in B-cell chronic lymphocytic leukemia.
Cancer genetics and cytogenetics 1988;36(2):203-4.
1988: Iurlo A; Mecucci C; Van Orshoven A; Michaux J L; Boogaerts M; Van den Berghe H
The karyotype in secondary hematologic disorders after treatment for Hodgkin's disease. A study of 19 patients.
Cancer genetics and cytogenetics 1988;36(2):165-72.
1988: Iurlo A; Mecucci C; Van Orshoven A; Michaux J L; Van den Berghe H
Inversion (4)(p13q28) in two cases of acute nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1988;36(2):143-7.
1988: Rege-Cambrin G; Mecucci C; Kerim S; Scaravaglio P; Boogaerts M; Van den Berghe H
Translocation t(11;21)(q24;q11.2) is a new nonrandomly occurring chromosome change in myelodysplastic syndromes.
Cancer genetics and cytogenetics 1988;34(1):33-40.
1988: Mecucci C; Michaux J L; Louwagie A; Boogaerts M; Van den Berghe H
The short arm of chromosome 6 is nonrandomly rearranged in secondary myelodysplastic syndromes.
Cancer genetics and cytogenetics 1988;31(2):147-55.
1988: Mecucci C; Louwagie A; Thomas J; Boogaerts M; Van Den Berghe H
Cytogenetic studies in T-cell malignancies.
Cancer genetics and cytogenetics 1988;30(1):63-71.
1988: Mecucci C; Noens L; Aventin A; Testoni N; Van den Berghe H
Philadelphia-positive acute myelomonocytic leukemia with inversion of chromosome 16 and eosinobasophils.
American journal of hematology 1988;27(1):69-71.
1987: Louwagie A C; Mecucci C; Criel A; Van Hoof A; Van den Berghe H
Variant translocation t(15q;17q) accompanying a promyelocytic accelerated phase of Ph-positive chronic myeloid leukemia.
Cancer genetics and cytogenetics 1987;28(2):349-52.
1987: Mecucci C; Van Orshoven A; Vermaelen K; Michaux J L; Tricot G; Louwagie A; Delannoy A; Van den Berghe H
11q-chromosome is associated with abnormal iron stores in myelodysplastic syndromes.
Cancer genetics and cytogenetics 1987;27(1):39-44.
1987: Aventin A; Mecucci C; Petrick M; Noens L; van den Berghe H
Masqued Philadelphia chromosome involving the short arm of chromosome 10.
Blut 1987;54(6):371-2.
1987: Rege-Cambrin G; Mecucci C; Tricot G; Michaux J L; Louwagie A; Van Hove W; Francart H; Van den Berghe H
A chromosomal profile of polycythemia vera.
Cancer genetics and cytogenetics 1987;25(2):233-45.
1987: Van den Berghe H; Mecucci C
Some karyotypic aspects of human leukemia.
Haematology and blood transfusion 1987;31():136-40.
1986: Mecucci C; Van Orshoven A; Tricot G; Michaux J L; Delannoy A; Van den Berghe H
Trisomy 4 identifies a subset of acute nonlymphocytic leukemias.
Blood 1986;67(5):1328-32.
1985: Van den Berghe H; Vermaelen K; Mecucci C; Barbieri D; Tricot G
The 5q-anomaly.
Cancer genetics and cytogenetics 1985;17(3):189-255.
1985: Louwagie A; Criel A; Verfaillie C M; Valcke Y J; Lamberts H; Hidajat M; Mecucci C; Van den Berghe H
Philadelphia-positive T-acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 1985;16(4):297-300.
1984: Mecucci C; Vermaelen K; Kulling G; Michaux J L; Noens L; Van Hove W; Tricot G; Louwagie A; Van den Berghe H
Interstitial 9q- deletions in hematologic malignancies.
Cancer genetics and cytogenetics 1984;12(4):309-19.
1984: Van den Berghe H; Vermaelen K; Louwagie A; Criel A; Mecucci C; Vaerman J P
High incidence of chromosome abnormalities in IgG3 myeloma.
Cancer genetics and cytogenetics 1984;11(4):381-7.
1983: Mecucci C; Vermaelen K; Tricot G; Louwagie A; Michaux J L; Bosly A; Thomas J; Barbieri D; Van den Berghe H
3q-, 3q+ anomaly in malignant proliferations in humans.
Cancer genetics and cytogenetics 1983;9(4):376-81.

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