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Results: 1-25 | 26-45
Results: 1-25/45
EFFECT OF TREATMENT WITH PROPRANOLOL ON Q-T INTERVAL PROLONGATION IN CIRRHOSIS
Authors: CALANDRA S CAPUTO F LONGO G RAIMONDO G
Citation: S. Calandra et al., EFFECT OF TREATMENT WITH PROPRANOLOL ON Q-T INTERVAL PROLONGATION IN CIRRHOSIS, Hepatology, 28(4), 1998, pp. 1579-1579
Q-T INTERVAL PROLONGATION IN CIRRHOSIS - PREVALENCE, RELATIONSHIP WITH SEVERITY, AND ETIOLOGY OF THE DISEASE AND POSSIBLE PATHOGENETIC FACTORS
Authors: BERNARDI M CALANDRA S COLANTONI A TREVISANI F RAIMONDO ML SICA G SCHEPIS F MANDINI M SIMONI P CONTIN M RAIMONDO G
Citation: M. Bernardi et al., Q-T INTERVAL PROLONGATION IN CIRRHOSIS - PREVALENCE, RELATIONSHIP WITH SEVERITY, AND ETIOLOGY OF THE DISEASE AND POSSIBLE PATHOGENETIC FACTORS, Hepatology, 27(1), 1998, pp. 28-34
SINUS ARREST DURING TACROLIMUS TREATMENT - WAS THE QT INTERVAL PROLONGED
Authors: CALANDRA S
Citation: S. Calandra, SINUS ARREST DURING TACROLIMUS TREATMENT - WAS THE QT INTERVAL PROLONGED, Transplantation, 66(3), 1998, pp. 402-403
ANALYSIS OF 2 DUPLICATIONS OF THE LDL RECEPTOR GENE AFFECTING INTRACELLULAR-TRANSPORT, CATABOLISM, AND SURFACE BINDING OF THE LDL RECEPTOR
Authors: PATEL DD LELLI N GARUTI R VOLTI SL BERTOLINI S KNIGHT BL CALANDRA S
Citation: Dd. Patel et al., ANALYSIS OF 2 DUPLICATIONS OF THE LDL RECEPTOR GENE AFFECTING INTRACELLULAR-TRANSPORT, CATABOLISM, AND SURFACE BINDING OF THE LDL RECEPTOR, Journal of lipid research, 39(7), 1998, pp. 1466-1475
SIMPLE DETECTION OF A POINT MUTATION IN LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN SOUTHERN ITALY BY ALLELE-SPECIFIC POLYMERASE-CHAIN-REACTION
Authors: CANTAFORA A BLOTTA I MERCURI E CALANDRA S BERTOLINI S
Citation: A. Cantafora et al., SIMPLE DETECTION OF A POINT MUTATION IN LDL RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN SOUTHERN ITALY BY ALLELE-SPECIFIC POLYMERASE-CHAIN-REACTION, Journal of lipid research, 39(5), 1998, pp. 1101-1105
SECRETION OF APO-B-CONTAINING AND APOA-I-CONTAINING LIPOPROTEINS BY CHICK KIDNEY
Authors: TARUGI P BALLARINI G PINOTTI B FRANCHINI A OTTAVIANI E CALANDRA S
Citation: P. Tarugi et al., SECRETION OF APO-B-CONTAINING AND APOA-I-CONTAINING LIPOPROTEINS BY CHICK KIDNEY, Journal of lipid research, 39(4), 1998, pp. 731-743
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
EFFECT OF HEPARIN ON CELL-PROLIFERATION - LACK OF CORRELATION WITH HEPARIN-BINDING SITES ON CELL-MEMBRANE
Authors: TIOZZO R REGGIANI D CROCE MA CALANDRA S OSIMA B BIANCHINI P
Citation: R. Tiozzo et al., EFFECT OF HEPARIN ON CELL-PROLIFERATION - LACK OF CORRELATION WITH HEPARIN-BINDING SITES ON CELL-MEMBRANE, Drugs under experimental and clinical research, 23(3-4), 1997, pp. 103-109
INFLUENCE OF HBSAG AND ANTI-HCV STATUS ON THE DIAGNOSTIC-ACCURACY OF ALPHA(1)-FETOPROTEIN (AFP) IN PATIENTS WITH CHRONIC LIVER-DISEASE
Authors: TREVISANI F MORSELLILABATE AM CALANDRA S DENOTARIIS S DINTINO PE ACCOGLI E MAZZELLA PG CARACENI P RAIMONDO G BERNARDI M
Citation: F. Trevisani et al., INFLUENCE OF HBSAG AND ANTI-HCV STATUS ON THE DIAGNOSTIC-ACCURACY OF ALPHA(1)-FETOPROTEIN (AFP) IN PATIENTS WITH CHRONIC LIVER-DISEASE, Hepatology, 26(4), 1997, pp. 173-173
4 NOVEL MUTATIONS OF STEROL 27-HYDROXYLASE GENE IN ITALIAN PATIENTS WITH CEREBROTENDINOUS XANTHOMATOSIS
Authors: GARUTI R CROCE MA TIOZZO R DOTTI MT FEDERICO A BERTOLINI S CALANDRA S
Citation: R. Garuti et al., 4 NOVEL MUTATIONS OF STEROL 27-HYDROXYLASE GENE IN ITALIAN PATIENTS WITH CEREBROTENDINOUS XANTHOMATOSIS, Journal of lipid research, 38(11), 1997, pp. 2322-2334
DEVELOPMENT OF RAPID TESTS FOR POINT MUTATIONS IN LDL-RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN SOUTHERN ITALY
Authors: CANTAFORA A BLOTTA I MERCURI E CALANDRA S BERTOLINI S
Citation: A. Cantafora et al., DEVELOPMENT OF RAPID TESTS FOR POINT MUTATIONS IN LDL-RECEPTOR GENE CAUSING FAMILIAL HYPERCHOLESTEROLEMIA IN SOUTHERN ITALY, Atherosclerosis, 135, 1997, pp. 8-8
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 TETRANUCLEOTIDE INSERTION IN EXON-8 OF LDL-RECEPTOR GENE IN AN ITALIAN FH PATIENT
Authors: RAMPA P MOTTI C TROVATELLO G BERNARDINI S MASSOUD R FUCCI G FEDERICI G CALANDRA S BERTOLINI S CORTESE C
Citation: P. Rampa et al., A TETRANUCLEOTIDE INSERTION IN EXON-8 OF LDL-RECEPTOR GENE IN AN ITALIAN FH PATIENT, Atherosclerosis, 135, 1997, pp. 19-19
SYNTHESIS AND SECRETION OF APOLIPOPROTEIN B-100 AND A-I BY CHICK KIDNEY
Authors: TARUGI P BALLARINI G PINOTTI B CALANDRA S
Citation: P. Tarugi et al., SYNTHESIS AND SECRETION OF APOLIPOPROTEIN B-100 AND A-I BY CHICK KIDNEY, Atherosclerosis, 134(1-2), 1997, pp. 20-21
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
MOLECULAR-GENETICS OF FAMILIAL HYPERCHOLESTEROLEMIA IN ITALY - OUTCOMES AND FUTURE-PROSPECTS
Authors: CALANDRA S BERTOLINI S
Citation: S. Calandra et S. Bertolini, MOLECULAR-GENETICS OF FAMILIAL HYPERCHOLESTEROLEMIA IN ITALY - OUTCOMES AND FUTURE-PROSPECTS, Atherosclerosis, 134(1-2), 1997, pp. 110-110
ABNORMAL LDL METABOLISM IN A CASE OF RECESSIVE FORM OF FAMILIAL HYPERCHOLESTEROLEMIA
Authors: PREVIATO L MARTINI S GABELLI C CORTELLA I CALANDRA S BAGGIO G CREPALDI G BERTOLINI S
Citation: L. Previato et al., ABNORMAL LDL METABOLISM IN A CASE OF RECESSIVE FORM OF FAMILIAL HYPERCHOLESTEROLEMIA, Atherosclerosis, 134(1-2), 1997, pp. 353-353
IN-VIVO LDL KINETIC AND IN-VITRO LDL METABOLISM IN A CASE OF RECESSIVE FAMILIAL HYPERCHOLESTEROLEMIA (RFH)
Authors: CORTELLA I GABELLI C BERTOLINI S MARTINI S CALANDRA S PREVIATO L CREPALDI G
Citation: I. Cortella et al., IN-VIVO LDL KINETIC AND IN-VITRO LDL METABOLISM IN A CASE OF RECESSIVE FAMILIAL HYPERCHOLESTEROLEMIA (RFH), Atherosclerosis, 133(2), 1997, pp. 24-24
VARIABLE PHENOTYPIC-EXPRESSION OF THE MUTATION PADUA-1 OF LDL-R GENE IN HOMOZYGOUS PATIENTS
Authors: DEMATTEI S ROLLERI R GARUTI R GINOCCHIO E MASTURZO P MARTINI S CASELLA F BAGGIO G CALANDRA S BERTOLINI S
Citation: S. Demattei et al., VARIABLE PHENOTYPIC-EXPRESSION OF THE MUTATION PADUA-1 OF LDL-R GENE IN HOMOZYGOUS PATIENTS, Atherosclerosis, 133(2), 1997, pp. 26-26
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
CEREBROTENDINOUS XANTHOMATOSIS CAUSED BY 2 NEW MUTATIONS OF THE STEROL-27-HYDROXYLASE GENE THAT DISRUPT MESSENGER-RNA SPLICING
Authors: GARUTI R LELLI N BAROZZINI M TIOZZO R DOTTI MT FEDERICO A OTTOMANO AM CROCE A BERTOLINI S CALANDRA S
Citation: R. Garuti et al., CEREBROTENDINOUS XANTHOMATOSIS CAUSED BY 2 NEW MUTATIONS OF THE STEROL-27-HYDROXYLASE GENE THAT DISRUPT MESSENGER-RNA SPLICING, Journal of lipid research, 37(7), 1996, pp. 1459-1467
SYNTHESIS AND SECRETION OF B-100 AND A-I APOLIPOPROTEINS IN RESPONSE TO THE CHANGES OF INTRACELLULAR CHOLESTERYL ESTER CONTENT IN CHICK LIVER
Authors: TARUGI P NICOLINI S BALLARINI G MARCHI L DUVIGNEAU C TARTONI P CALANDRA S
Citation: P. Tarugi et al., SYNTHESIS AND SECRETION OF B-100 AND A-I APOLIPOPROTEINS IN RESPONSE TO THE CHANGES OF INTRACELLULAR CHOLESTERYL ESTER CONTENT IN CHICK LIVER, Journal of lipid research, 37(3), 1996, pp. 493-507
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