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Results: 1-13 |
Results: 13
A DE-NOVO POINT MUTATION OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENEIN AN ITALIAN SUBJECT WITH PRIMARY HYPERCHOLESTEROLEMIA
Authors: CASSANELLI S BERTOLINI S ROLLERI M DESTEFANO F CASARINO L ELICIO N NASELLI A CALANDRA S
Citation: S. Cassanelli et al., A DE-NOVO POINT MUTATION OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENEIN AN ITALIAN SUBJECT WITH PRIMARY HYPERCHOLESTEROLEMIA, Clinical genetics, 53(5), 1998, pp. 391-395
FH CLUSTERS IN SOUTHERN ITALY
Authors: FASCETTI V ROLLERI M GUIDO V TROVATELLO G MASTURZO P GARUTI R MOTTI C CORTESE C CANTAFORA A CALANDRA S BERTOLINI S
Citation: V. Fascetti et al., FH CLUSTERS IN SOUTHERN ITALY, Atherosclerosis, 135, 1997, pp. 12-12
A FOUNDER-RELATED LDL RECEPTOR GENE MUTATION IN THE LIGURIA REGION OFITALY
Authors: DEMATTEI S ROLLERI M MASTURZO P FASCETTI V ELICIO N MOTTI C CORTESE C CALANDRA S BERTOLINI S
Citation: S. Demattei et al., A FOUNDER-RELATED LDL RECEPTOR GENE MUTATION IN THE LIGURIA REGION OFITALY, Atherosclerosis, 134(1-2), 1997, pp. 66-66
A DE-NOVO POINT MUTATION OF LDL RECEPTOR GENE
Authors: GARUTI R ROLLERI M BERTOLINI S DESTEFANO F CASARINO L CALANDRA S
Citation: R. Garuti et al., A DE-NOVO POINT MUTATION OF LDL RECEPTOR GENE, Atherosclerosis, 134(1-2), 1997, pp. 67-67
FAMILIAL HYPOBETALIPOPROTEINEMIA CAUSED BY A TRUNCATED APOLIPOPROTEIN-B (B-33.4) IS NOT PROTECTIVE AGAINST CAROTID-ARTERY DISEASE
Authors: GABELLI C BERTOLINI S ROLLERI M MARANGONI A PREVIATO L MARTINI S CORTELLA I BAGGIO G CREPALDI G
Citation: C. Gabelli et al., FAMILIAL HYPOBETALIPOPROTEINEMIA CAUSED BY A TRUNCATED APOLIPOPROTEIN-B (B-33.4) IS NOT PROTECTIVE AGAINST CAROTID-ARTERY DISEASE, Atherosclerosis, 134(1-2), 1997, pp. 67-67
NEW MINUTE OR POINT MUTATIONS OF LDL-R GENE IN PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
Authors: GINOCCHIO E ROLLERI M GARUTI R MASTURZO P GUIDO V ELICIO N CORTESE C MOTTI C CALANDRA S BERTOLINI S
Citation: E. Ginocchio et al., NEW MINUTE OR POINT MUTATIONS OF LDL-R GENE IN PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA, Atherosclerosis, 133(2), 1997, pp. 30-30
A NEW MUTATION OF THE LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE CAUSING FISH-EYE DISEASE
Authors: ROLLERI M TARUGI P MASTURZO P GINOCCHIO E FASCETTI V FRANCESCHINI G FUNKE H CALANDRA S BERTOLINI S
Citation: M. Rolleri et al., A NEW MUTATION OF THE LECITHIN-CHOLESTEROL ACYLTRANSFERASE (LCAT) GENE CAUSING FISH-EYE DISEASE, Atherosclerosis, 133(2), 1997, pp. 51-51
THE DD GENOTYPE OF THE ACE GENE, BUT NOT THE VAL VAL GENOTYPE OF THE MTHFR GENE, IS STRONGLY ASSOCIATED WITH CHD IN SUBJECTS WITH HETEROZYGOUS FH/
Authors: BERTOLINI S MASTURZO P ROLLERI M AMADEI L GINOCCHIO E GUIDO V CALANDRA S
Citation: S. Bertolini et al., THE DD GENOTYPE OF THE ACE GENE, BUT NOT THE VAL VAL GENOTYPE OF THE MTHFR GENE, IS STRONGLY ASSOCIATED WITH CHD IN SUBJECTS WITH HETEROZYGOUS FH/, Atherosclerosis, 129(1), 1997, pp. 34-34
4 NOVEL PARTIAL DELETIONS OF LDL-RECEPTOR GENE IN ITALIAN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA
Authors: BERTOLINI S GARUTI R LELLI W ROLLERI M TIOZZO RM GHISELLINI M SIMONE ML MASTURZO P ELICIO NC STEFANUTTI C COVIELLO D CARABBIO C ORECCHINI G CALANDRA S
Citation: S. Bertolini et al., 4 NOVEL PARTIAL DELETIONS OF LDL-RECEPTOR GENE IN ITALIAN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA, Arteriosclerosis, thrombosis, and vascular biology, 15(1), 1995, pp. 81-88
APOLIPOPROTEIN-E EPSILON-4 ALLELE FREQUENCY IS NOT INCREASED IN PROGRESSIVE SUPRANUCLEAR PALSY
Authors: TABATON M ROLLERI M MASTURZO P CAMMARATA S ANGELINI G HANSEN LA SAITOH T PETERSON RB PERRY G RICHEY P GAMBETTI P BERTOLINI S
Citation: M. Tabaton et al., APOLIPOPROTEIN-E EPSILON-4 ALLELE FREQUENCY IS NOT INCREASED IN PROGRESSIVE SUPRANUCLEAR PALSY, Neurology, 45(9), 1995, pp. 1764-1765
OCCURRENCE OF MULTIPLE ABERRANTLY SPLICED MESSENGER-RNAS OF THE LDL-RECEPTOR GENE UPON A DONOR SPLICE-SITE MUTATION THAT CAUSES FAMILIAL HYPERCHOLESTEROLEMIA (FHBENEVENTO)
Authors: LELLI N GARUTI R GHISELLINI M TIOZZO R ROLLERI M AIMALE V GINOCCHIO E NASELLI A BERTOLINI S CALANDRA S
Citation: N. Lelli et al., OCCURRENCE OF MULTIPLE ABERRANTLY SPLICED MESSENGER-RNAS OF THE LDL-RECEPTOR GENE UPON A DONOR SPLICE-SITE MUTATION THAT CAUSES FAMILIAL HYPERCHOLESTEROLEMIA (FHBENEVENTO), Journal of lipid research, 36(6), 1995, pp. 1315-1324
A NEW MISSENSE MUTATION (CYS(297)-]PHE) OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR IN ITALIAN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA (FH(TRIESTE))
Authors: LELLI N GARUTI R PEDRAZZI P GHISELLINI M SIMONE ML TIOZZO R CATTIN L VALENTI M ROLLERI M BERTOLINI S STEFANUTTI C CALANDRA S
Citation: N. Lelli et al., A NEW MISSENSE MUTATION (CYS(297)-]PHE) OF THE LOW-DENSITY-LIPOPROTEIN RECEPTOR IN ITALIAN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA (FH(TRIESTE)), Human genetics, 93(5), 1994, pp. 538-540
ACCURATE MOVEMENT TO REMEMBERED TARGETS - NORMAL VERSUS PARKINSONIAN-PATIENTS
Authors: HENING WA ROLLERI M GORDON J
Citation: Wa. Hening et al., ACCURATE MOVEMENT TO REMEMBERED TARGETS - NORMAL VERSUS PARKINSONIAN-PATIENTS, Annals of neurology, 34(2), 1993, pp. 267-267
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