Výsledky vyhledávání - "M. G. Roberti"

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

Autor: A, Cuneo, R, Bigoni, M G, Roberti, R, Milani, P, Agostini, F, Cavazzini, C, Minotto, De Angeli C, A, Bardi, E, Tammiso, M, Negrini, P, Cavazzini, G, Castoldi

Publikováno v: Haematologica. 86(1)

To improve the definition of the incidence and significance of chromosome lesions occurring in marginal zone B-cell lymphoma (MZBCL).Fourteen cases of MZBCL diagnosed according to the REAL classification were studied by conventional chromosome analys

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::563354cefb65036b73d42f099e71cf8f
https://pubmed.ncbi.nlm.nih.gov/11146573

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

Autor: C, De Angeli, D, Gandini, A, Cuneo, S, Moretti, R, Bigoni, M G, Roberti, A, Bardi, G L, Castoldi, L, del Senno

Publikováno v: Haematologica. 85(9)

The translocation t(11;14) (q13;q32), typically described in mantle cell lymphomas (MCL), has also been found in some cases of non-MCL lymphoproliferative disorders, such as splenic lymphoma with villous lymphocytes (SLVL), multiple myeloma (MM), pro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::267722b991fedd28103a6f8527725ece
https://pubmed.ncbi.nlm.nih.gov/10980628

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

Autor: R, Bigoni, A, Cuneo, M G, Roberti, R, Milani, A, Bardi, F, Cavazzini, C, Minotto, G, Castoldi

Publikováno v: Haematologica. 85(5)

Idiopathic hypereosinophilic syndrome (HES) is defined as a peripheral blood eosiniphilia greater than 1, 500 cells/microL for longer than 6 months, absence of other apparent etiologies for eosinophilia and signs and symptoms of organ involvement. HE

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0761e6f0f95402f5241c17bf2edec43c
https://pubmed.ncbi.nlm.nih.gov/10800164

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

Autor: A, Cuneo, M G, Roberti, R, Bigoni, C, Minotto, A, Bardi, R, Milani, A, Tieghi, D, Campioni, F, Cavazzini, C, De Angeli, M, Negrini, G, Castoldi

Publikováno v: British journal of haematology. 108(3)

Nine patients with previously unreported chromosome changes were identified among 209 B-cell chronic lymphocytic leukaemia (CLL) cases: three patients had a translocation involving 6p24-25; three had a 12p12-13 translocation; two had 4q21 involvement

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c5c788e94ab1f37bf0a70466f4ba0ea4
https://pubmed.ncbi.nlm.nih.gov/10759714

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13q14 deletion in non-Hodgkin's lymphoma: correlation with clinicopathologic features

Autor: A, Cuneo, R, Bigoni, G M, Rigolin, M G, Roberti, A, Bardi, D, Campioni, C, Minotto, P, Agostini, R, Milani, F, Bullrich, M, Negrini, C, Croce, G, Castoldi

Publikováno v: Haematologica. 84(7)

13q14 deletion frequently occurs as a single anomaly in chronic lymphocytic leukemia (CLL) with favorable prognosis. This study was performed to assess the distribution of 13q14 deletion in non-Hodgkin's lymphoma (NHL) and to analyze its correlation

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8eb2371dc8379dba9ff37c114b8b2161
https://pubmed.ncbi.nlm.nih.gov/10406898

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

Autor: G M, Rigolin, A, Cuneo, M G, Roberti, A, Bardi, R, Bigoni, N, Piva, C, Minotto, P, Agostini, C, De Angeli, L, Del Senno, R, Spanedda, G, Castoldi

Publikováno v: British journal of haematology. 103(1)

To better define the role of exposure to myelotoxic agents in the genesis of myelodysplastic syndrome (MDS), we carried out (a) a case-control study for the determination of the relative risk (RR) of developing MDS, including 178 consecutive patients

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::097c0a1a5d0290e433471a7f119e1d97
https://pubmed.ncbi.nlm.nih.gov/9792307

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

Autor: A, Cuneo, R, Bigoni, M G, Roberti, A, Bardi, G M, Rigolin, N, Piva, M, Mancini, M, Nanni, G, Alimena, C, Mecucci, C, Matteucci, R, La Starza, P, Bernasconi, P, Cavigliano, E, Genini, A, Zaccaria, N, Testoni, C, Carboni, G, Castoldi

The role of fluorescence in situ hybridization (FISH) in the detection and monitoring of trisomy 8 (+8) in acute myelogenous leukemia (AML) has not been defined exactly. This multicentric study was performed in order to: i) analyze the sensitivity of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e5d68c2053311f1c867d8c6d9adec8b4
http://hdl.handle.net/11573/31797

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