Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Gian Franco Gaetani"'
Autor:
Maurizio Miglino, Letizia Canepa, Anna Maria Ferraris, Gian Franco Gaetani, Cecilia Melani, Mario Sessarego
Publikováno v:
European Journal of Haematology. 42:32-37
We describe here a patient with Ph'-positive chronic myelogenous leukemia (CML) who developed a Ph'-negative blastic crisis. The blast DNA was analyzed on two different occasions, at the beginning of the blastic phase and at the end, shortly before t
Autor:
Gian Franco Gaetani, Omar Racchi, Laura Sticchi, Davide Rapezzi, Rosa Mangerini, Anna Maria Ferraris
Publikováno v:
European Journal of Haematology. 70:225-230
Objective: Vaccination against influenza in patients with chronic lymphoproliferative disorders (CLPD) and multiple myeloma (MM) is still a matter of clinical uncertainty. The aim of this study was to determine the safety, immunogenicity and clinical
Autor:
Davide Rapezzi, Anna Maria Ferraris, Rosa Mangerini, Michela Rolfo, Gian Franco Gaetani, Omar Racchi
Publikováno v:
British Journal of Haematology. 119:833-838
Summary. Methylene blue (MB) is a powerful reducing agent that is widely used in clinical practice as well as for metabolic studies of the erythrocyte. We have investigated the role of catalase as a specific enzyme for the removal of hydrogen peroxid
Publikováno v:
Annals of Hematology. 80:340-344
The relative incidence of Hodgkin's disease (HD) has been found to have increased approximately seven times in HIV-infected patients. We analyzed the histological distribution of HIV-associated HD with the aim of clarifying purported difference(s) fr
Publikováno v:
The American Journal of Human Genetics. 61:458-461
High telomerase activity in granulocytes from clonal polycythemia vera and essential thrombocythemia
Autor:
Salvatore Casciaro, Gian Franco Gaetani, Natalija Pujic, Omar Racchi, Rosa Mangerini, Davide Rapezzi, Andrea Gallamini, Anna Maria Ferraris
Publikováno v:
Blood. 105:2138-2140
Essential thrombocythemia (ET) and polycythemia vera (PV) are chronic myeloproliferative disorders that share the involvement of a multipotent progenitor cell and dominance of the transformed clone over normal hematopoiesis. On the other hand, the he
Autor:
Gian Franco Gaetani, Anna Maria Ferraris, Sara Arena, Rosa Mangerini, Henry N. Kirkman, Michela Rolfo
Publikováno v:
Blood. 87:1595-1599
Purified enzymes were mixed to form a cell-free system that simulated the conditions for removal of hydrogen peroxide within human erythrocytes. Human glutathione peroxidase disposed of hydrogen peroxide (H2O2) at a rate that was only 17% of the rate
Publikováno v:
Blood. 84:325-330
The catalase within normal, intact human erythrocytes was completely inactivated with amino triazole. The rate of 14CO2 evolution, when the cells were subsequently incubated with 14C-labeled glucose, provided a measure of the rate at which NADPH was
Publikováno v:
British Journal of Haematology. 82:745-752
Congenital dyserythropoietic anaemia type II, or HEMPAS (hereditary erythroblastic multinuclearity with positive acidified serum lysis test) is a genetic disease caused by membrane disorganization of erythroid cells. The primary defect of this diseas
Publikováno v:
Biochimica et Biophysica Acta (BBA) - General Subjects. 1074:101-104
We have measured, by a sensitive cycling assay, the concentration of bound and unbound dinucleotides in normal and glucose-6-phosphate dehydrogenase (G6PD)-deficient erythrocytes. Measurement of free NADP in ultrafiltrates confirms that in normal ery