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Results: 1-7 |
Results: 7
The apolipoprotein E genotype in patients affected by syndromes with focalcortical atrophy (vol 303, pg 87, 2001)
Authors: Masullo, C Daniele, A Fazio, VM Seripa, D Gravina, C Filippini, V Grossi, D Fragassi, NA Nichelli, P Leone, M Gainotti, G
Citation: C. Masullo et al., The apolipoprotein E genotype in patients affected by syndromes with focalcortical atrophy (vol 303, pg 87, 2001), NEUROSCI L, 308(1), 2001, pp. 66-66
The Apolipoprotein E genotype in patients affected by syndromes with focalcortical atrophy
Authors: Masullo, C Daniele, A Fazio, VM Seripa, D Gravina, C Filippini, V Grossi, D Fragassi, N Nichelli, P Leone, M Gainotti, G
Citation: C. Masullo et al., The Apolipoprotein E genotype in patients affected by syndromes with focalcortical atrophy, NEUROSCI L, 303(2), 2001, pp. 87-90
Sensitive detection of transitional cell carcinoma of the bladder by microsatellite analysis of cells exfoliated in urine
Authors: Seripa, D Parrella, P Gallucci, M Gravina, C Papa, S Fortunato, P Alcini, A Flammia, G Lazzari, M Fazio, VM
Citation: D. Seripa et al., Sensitive detection of transitional cell carcinoma of the bladder by microsatellite analysis of cells exfoliated in urine, INT J CANC, 95(6), 2001, pp. 364-369
Ext-mutation analysis in Italian sporadic and hereditary osteochondromas
Authors: Gigante, M Matera, MG Seripa, D Izzo, AM Venanzi, R Giannotti, A Digilio, MC Gravina, C Lazzari, M Monteleone, G Monteleone, M Dallapiccola, B Fazio, VM
Citation: M. Gigante et al., Ext-mutation analysis in Italian sporadic and hereditary osteochondromas, INT J CANC, 95(6), 2001, pp. 378-383
Treatment of severe hypercholesterolemia in apolipoprotein E-deficient mice by intramuscular injection of plasmid DNA
Authors: Rinaldi, M Catapano, AL Parrella, P Ciafre, SA Signori, E Seripa, D Uboldi, P Antonini, R Ricci, G Farace, MG Fazio, VM
Citation: M. Rinaldi et al., Treatment of severe hypercholesterolemia in apolipoprotein E-deficient mice by intramuscular injection of plasmid DNA, GENE THER, 7(21), 2000, pp. 1795-1801
A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing
Authors: Margaglione, M Santacroce, R Colaizzo, D Seripa, D Vecchione, G Lupone, MR De Lucia, D Fortina, P Grandone, E Perricone, C Di Minno, G
Citation: M. Margaglione et al., A G-to-A mutation in IVS-3 of the human gamma fibrinogen gene causing afibrinogenemia due to abnormal RNA splicing, BLOOD, 96(7), 2000, pp. 2501-2505
Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinemia patients and in the general population from Southern Italy
Authors: Seripa, D Gravina, C Volpe, R Margaglione, M Papa, S Merla, G Parrella, P Di Minno, G Ricci, G Testa, M Fazio, VM
Citation: D. Seripa et al., Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinemia patients and in the general population from Southern Italy, J INH MET D, 22(5), 1999, pp. 670-671
Risultati: 1-7 |