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Insulin receptor binding on red cells of hypertriglyceridemic patients. Effect of a low fat, low carbohydrate diet. 1-gen-1985 Cordera, Renzo; Bertolini, Stefano; Andraghetti, Gabriella; Pistocchi, G; de Alessi, M; Gherzi, R.
Effects of three low-dose oral contraceptive formulations on lipid metabolism. 1-gen-1987 Bertolini, Stefano; Elicio, Nicola; Cordera, Renzo; Gapitanio, Gl; Montagna, G; Croce, S; Saturnino, M; Balestreri, Roberto; De Cecco, L.
Blood and synovial levels of piroxicam and their effects on some metabolites of arachidonic acid 1-gen-1987 D., Fasciolo; M. L., Maglio; Bertolini, Stefano; S., Accardo; Seriolo, Bruno; Parodi, Brunella; S., Cafaggi; G., Bignardi
Pvu II polymorphism of low density lipoprotein receptor gene and familial hypercholesterolemia. Study of Italians. 1-gen-1988 Daga, A; Fabbi, M; Mattioni, T; Bertolini, Stefano; Corte, G.
Use of three DNA polymorphisms of the LDL-receptor gene in the diagnosis of Familial Hypercholesterolemia. 1-gen-1990 Daga, A; Mattioni, T; Coviello, Da; Balestreri, R; Corte, G; Bertolini, Stefano
Duplication of exons 13, 14 and 15 of LDL-receptor gene in a patient with heterozygous Familial Hypercholesterolemia. 1-gen-1991 Lelli, N; Ghisellini, M; Calandra, S; Gaddi, A; Ciarocchi, A; Coviello, Da; Bertolini, Stefano
Characterization of three mutations of LDL-receptor gene in Italians patients with Familial Hypercholesterolemia. 1-gen-1991 Lelli, N; Ghisellini, M; Gualdi, R; Tiozzo, R; Calandra, S; Gaddi, A; Ciarrocchi, A; Arca, M; Fazio, S; Coviello, Da; Bertolini, Stefano
Variation in the LDL-receptor gene is associated with differences in plasma LDL-cholesterol levels in young and old normal individuals from Italy. 1-gen-1991 Humphries, S; Coviello, Da; Masturzo, Paola; Balestreri, Roberto; Orecchini, G; Bertolini, Stefano
HEMORHEOLOGICAL AND CEREBRAL BLOOD FLOW CHANGES INDUCED BY LDL- APHERESIS IN FAMILIAL HYPERCHOLESTEROLEMIC PATIENTS. 1-gen-1991 Nobili, FLAVIO MARIANO; Bertolini, Stefano; Elicio, N; Francione, S; Marenco, S; Rodriguez, Guido; Tortorolo, U; Viale, Pa; Rosadini, G.
A large deletion in the LDL-receptor gene. The cause of Familial Hypercholesterolemia in three italian families: a study that dates back to the 17th century (FH Pavia). 1-gen-1992 Bertolini, Stefano; Lelli, N; Coviello, Da; Ghisellini, M; Masturzo, Paola; Tiozzo, R; Elicio, N; Gaddi, A; Calandra, S.
Alternative splicing of mutant LDL-receptor mRNA in an Italian patient with familial hypercholesterolemia due to a partial deletion of LDL-receptor gene (FH Potenza). 1-gen-1993 Lelli, N; Garuti, R; Zambelli, F; Cassanelli, R; Tiozzo, R; Corsini, A; Bertolini, Stefano; Riva, E; Ortisi, Mt; Bell, R; Calandra, S.
Chorionic DNA analysis for the prenatal diagnosis of familial hypercholesterolemia. 1-gen-1993 Coviello, Da; Bertolini, Stefano; Masturzo, Paola; Ghisellini, M; Tiozzo, R; Zambelli, F; Stefanutti, C; Torcia, F; Pachi', A; Ricci, G; Calandra, S.
Partial duplication of the EGF precursor homology domain of the LDL-receptor protein causing Familial Hypercholesterolemia (FH Salerno) 1-gen-1994 Bertolini, Stefano; Patell, Dd; Coviello, Da; Lelli, N; Ghisellini, M; Tiozzo, R; Masturzo, Paola; Elicio, N; Knight, Bl; Calandra, S.
Regional cerebral blood flow in familial hypercholesterolemia 1-gen-1994 Rodriguez, Guido; Bertolini, Stefano; Nobili, FLAVIO MARIANO; Arrigo, A; Masturzo, Paola; Elicio, N; Gambaro, M; Rosadini, G.
A new missense mutation (Cys297-->Phe) of the low density lipoprotein receptor in Italian patients with familial hypercholesterolemia (FHTrieste). 1-gen-1994 Lelli, N; Garuti, R; Pedrazzi, P; Ghisellini, M; Simone, Ml; Tiozzo, R; Cattin, L; Valenti, M; Rolleri, M; Bertolini, Stefano
Four novel partial deletions of LDL receptor gene in Italian patients with Familial Hypercholesterolemia 1-gen-1995 Bertolini, Stefano; Garuti, L.; Lelli, N.; Rolleri, M.; Tiozzo, R.; Ghisellini, M.; Simone, M. L.; Masturzo, Paola; Elicio, N.; Stefanutti, C.; Coviello, D. A.; Carabbio, C.; Calandra, S.
Occurrence of multiple aberrantly spliced mRNAs of LDL-receptor Gene upon a donor splice site mutation that causes Familial Hypercholesterolemia (FH-Benevento). 1-gen-1995 Lelli, N; Garuti, R; Ghisellini, M; Tiozzo, R; Rolleri, M; Aimale, V; Ginocchio, E; Naselli, A; Bertolini, Stefano; Calandra, S.
Apolipoprotein E4 allele frequency is not increased in progressive sopranuclear palsy 1-gen-1995 Tabaton, Massimo; Rolleri, M; Masturzo, Paola; Cammarata, S; Angelini, P; Hansen, La; Saiton, T; Petersen, Rb; Perry, G; Richey, P; Gambetti, P; Bertolini, Stefano
Mutant factor V (Arg506Gln) in healthy centenarians. 1-gen-1996 Mari, D; Mannucci, Pm; Duca, F; Bertolini, Stefano; Franceschi, C.
Cerebrotendinous xanthomatosis caused by two new mutations of sterol-27-hydroxylase gene that disrupt mRNA splicing. 1-gen-1996 Garuti, R; Lelli, N; Barozzini, M; Tiozzo, R; Dotti, Mt; Federico, A; Ottomano, Am; Croce, A; Bertolini, Stefano; Calandra, S.
Mostrati risultati da 1 a 20 di 138
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