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A case of chronic myelocytic leukemia with five Philadelphia chromosomesCASALONE, R; MASERATI, E.Cancer genetics and cytogenetics. 1988, Vol 34, Num 2, pp 257-259, issn 0165-4608Article

Stimulation of DNA synthesis by endothelin-1 in primary cultures of human dental pulpCASASCO, A; MASERATI, E; POLAK, J. M et al.Archives of oral biology. 1994, Vol 39, Num 3, pp 245-249, issn 0003-9969Article

Graft-versus-leukemia effects after allogeneic bone marrow transplantation are active also in the presence of clones with chromosomal anomalies in addition to the Ph chromosomeMASERATI, E; CASALI, M; FOGU, G et al.Cancer genetics and cytogenetics. 1992, Vol 61, Num 2, pp 152-157, issn 0165-4608Article

Meiotic origin of trisomy in neoplasms : evidence in a case of erythroleukaemiaMINELLI, A; MORERIO, C; PASQUALI, F et al.Leukemia. 2001, Vol 15, Num 6, pp 971-975, issn 0887-6924Article

Transposition of c-abl oncogene in a case of masked Ph chromosome duplicated in blastic phaseMASERATI, E; CAVALLI, P; CASALONE, R et al.Human genetics. 1988, Vol 78, Num 3, pp 248-250, issn 0340-6717Article

Different break-points in Philadelphia chromosome variant translocations and in constitutional and sporadic translocationsMASERATI, E; PASQUALI, F; PERETTI, D et al.Annals of human genetics. 1986, Vol 50, Num 2, pp 153-162, issn 0003-4800Article

Ring chromosome 9 with a 9p22.3-p24.3 duplicationSEGHEZZI, L; MARASCHIO, P; BOZZOLA, M et al.European journal of pediatrics. 1999, Vol 158, Num 10, pp 791-793, issn 0340-6199Article

Definition of an acquired 11q deletion in a tumorigenic human monocytic cell lineMASERATI, E; ROMITTI, L; CARROZZA, M. L et al.Human genetics. 1990, Vol 84, Num 4, pp 381-381, issn 0340-6717, 1 p.Article

Transferrin and structural anomalies of chromosome 3 in the blastic phase of chronic myelocytic leukemiaMASERATI, E; CAMPAGNOLI, E; TRUGLIO, F et al.Hereditas (Landskrona). 1989, Vol 111, Num 3, pp 305-308, issn 0018-0661Article

The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndromeMINELLI, A; MASERATI, E; CIPOLLI, M et al.Leukemia. 2009, Vol 23, Num 4, pp 708-711, issn 0887-6924, 4 p.Article

Centralized cytogenetic analysis of pediatric acute leukemia : Results of an Italian collaborative experienceSAINATI, L; LESZL, A; STELLA, M et al.Haematologica (Roma). 1997, Vol 82, Num 6, pp 654-659, issn 0390-6078Article

Busulfan, cyclophosphamide and melphalan as conditioning regimen for bone marrow transplantation in children with myelodysplastic syndromesLOCATELLI, F; PESSION, A; BONETTI, F et al.Leukemia. 1994, Vol 8, Num 5, pp 844-849, issn 0887-6924Article

Clinical, cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasiaLANZI, G; BALOTTIN, U; FRANCIOTTA, D et al.European neurology. 1992, Vol 32, Num 3, pp 121-125, issn 0014-3022Article

Cytogenetics in autologous bone marrow transplantationMASERATI, E; CAMPAGNOLI, E; TRUGLIO, F et al.Cancer genetics and cytogenetics. 1990, Vol 45, Num 1, pp 137-138, issn 0165-4608, 2 p.Article

Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndromeOLIVIERI, C; MARASCHIO, P; CASELLI, D et al.European journal of pediatrics. 2003, Vol 162, Num 2, pp 100-103, issn 0340-6199, 4 p.Article

Cerebellar dysgenesis and mental retardation associated with a complex chromosome rearrangementMASERATI, E; VERRI, A; SEGHEZZI, L et al.Annales de génétique (Paris). 1999, Vol 42, Num 4, pp 210-214, issn 0003-3995Conference Paper

Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic lossSEGHEZZI, L; DELLAVECCHIA, C; MASERATI, E et al.Cancer genetics and cytogenetics. 1997, Vol 99, Num 1, pp 77-80, issn 0165-4608Article

Translocation (8;21) in two cases of refractory anemia with excess of blasts in transformationMASERATI, E; CASALI, M; PASQUALI, F et al.Cancer genetics and cytogenetics. 1992, Vol 58, Num 1, pp 76-78, issn 0165-4608Article

Establishment and characterization of a B-cell line derived from a patient with a myelodysplastic syndrome which expresses myelomonocytic and lymphoid markersBERGAMASCHI, G; STELLA, C. C; CAZZOLA, M et al.British journal of haematology. 1991, Vol 78, Num 2, pp 167-172, issn 0007-1048Article

Myelodysplastic syndromes : the pediatric point of viewLOCATELLI, F; ZECCA, M; PESSION, A et al.Haematologica (Roma). 1995, Vol 80, Num 3, pp 268-279, issn 0390-6078Article

Roberts syndrome : phenotypic variation, cytogenetic definition and heterozygote detectionMASERATI, E; PASQUALI, F; ZUFFARDI, O et al.Annales de génétique (Paris). 1991, Vol 34, Num 3-4, pp 239-246, issn 0003-3995Article

A highly conserved sequence on the short arm of chromosome 7 detects multiple polymorphismsBARDONI, B; GUIOLI, S; MASERATI, E et al.Human genetics. 1988, Vol 81, Num 1, pp 23-25, issn 0340-6717Article

Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14MASERATI, E; OTTOLINI, A; VEGGIOTTI, P et al.Clinical genetics. 1988, Vol 34, Num 5, pp 283-287, issn 0009-9163Article

A 45,X male with a Yp/18 translocationMASERATI, E; WAIBEL, F; WOLF, U et al.Human genetics. 1986, Vol 74, Num 2, pp 126-132, issn 0340-6717Article

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