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Results: 1-13 |
Results: 13

Authors: Rizzio, E Bergamaschi, G Profumo, A Gallorini, M
Citation: E. Rizzio et al., The use of neutron activation analysis for particle size fractionation andchemical characterization of trace elements in urban air particulate matter, J RAD NUCL, 248(1), 2001, pp. 21-28

Authors: Bertelli, M Bergamaschi, G
Citation: M. Bertelli et G. Bergamaschi, The minor churches of the monastery of San-Salvatore in Brescia - The churches of Santa Giulia and San Nicola, NUOV RIV ST, 85(1), 2001, pp. 95-110

Authors: Bergamaschi, G Rolandi, V Cazzola, M
Citation: G. Bergamaschi et al., Differential HFE allele expression in hemochromatosis heterozygotes, GASTROENTY, 120(5), 2001, pp. 1308-1308

Authors: Cazzola, M Bergamaschi, G
Citation: M. Cazzola et G. Bergamaschi, Response: X chromosome inactivation ratios in female carriers of X-linked sideroblastic anemia, BLOOD, 97(12), 2001, pp. 4001-4002

Authors: Vercesi, E Cerani, P Rolandi, V Rovati, A Bergamaschi, G
Citation: E. Vercesi et al., Abnormal regulation of HFE mRNA expression may not contribute to primary iron overload, HAEMATOLOG, 85(8), 2000, pp. 787-791

Authors: Rosti, V Lucotti, C Cazzola, M Bergamaschi, G
Citation: V. Rosti et al., Inhibition of c-ABL expression in hematopoietic progenitor cells using antisense oligodeoxynucleotides, METH ENZYM, 314, 2000, pp. 429-440

Authors: Lucotti, C Malabarba, L Rosti, V Bergamaschi, G Danova, M Invernizzi, R Pecci, A Ramajoli, I Perotti, C Torretta, L De Amici, M Salvaneschi, L Cazzola, M
Citation: C. Lucotti et al., Cell cycle distribution of cord blood-derived haematopoietic progenitor cells and their recruitment into the S-phase of the cell cycle, BR J HAEM, 108(3), 2000, pp. 621-628

Authors: Cazzola, M May, A Bergamaschi, G Cerani, P Rosti, V Bishop, DF
Citation: M. Cazzola et al., Familial-skewed X-chromosome inactivation as a predisposing factor for late-onset X-linked sideroblastic anemia in carrier females, BLOOD, 96(13), 2000, pp. 4363-4365

Authors: Bergamaschi, G
Citation: G. Bergamaschi, Molecular basis of new disorders of iron metabolism in man, HAEMATOLOG, 84(6), 1999, pp. 481-482

Authors: Rovati, A Bergamaschi, G Casula, S Cerani, P Grasso, M Cazzola, M
Citation: A. Rovati et al., The dysmetabolic iron overload syndrome is clinically and genetically distinct from HFE-related genetic hemochromatosis, HAEMATOLOG, 84(2), 1999, pp. 182-183

Authors: Cazzola, M Beguin, Y Bergamaschi, G Guarnone, R Cerani, P Barella, S Cao, A Galanello, R
Citation: M. Cazzola et al., Soluble transferrin receptor as a potential determinant of iron loading incongenital anaemias due to ineffective erythropoiesis, BR J HAEM, 106(3), 1999, pp. 752-755

Authors: Frassoni, F Podesta, M Piaggio, G Rosti, V Pitto, A Benvenuto, F Figari, O Vassallo, F Carella, AM Zikos, P Bergamaschi, G Fugazza, G Sessarego, M Cazzola, M
Citation: F. Frassoni et al., Normal primitive haemopoietic progenitors are more frequent than their leukaemic counterpart in newly diagnosed patients with chronic myeloid leukaemia but rapidly decline with time, BR J HAEM, 104(3), 1999, pp. 538-545

Authors: Bobbio-Pallavicini, E Cannatelli, G Motta, E Grassi, M Bergamaschi, G Rosso, R Moroni, M
Citation: E. Bobbio-pallavicini et al., Histologic diagnosis and precocious treatment in a case of isolated promyelocytic sarcoma, LEUKEMIA, 12(12), 1998, pp. 2035-2036
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