Authors:
TURCO AE
ROSSETTI S
BRESIN E
ENGLISCH S
CORRA S
PIGNATTI PF
Citation: Ae. Turco et al., 3 NOVEL MUTATIONS OF THE PKD1 GENE IN ITALIAN FAMILIES WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE, Human mutation, 10(2), 1997, pp. 164-167
Authors:
LUPO A
MARCANTONI C
OLDRIZZI L
BRESIN E
MASCHIO G
Citation: A. Lupo et al., ACE GENE POLYMORPHISM AND CLINICAL AND MORPHOLOGICAL CORRELATIONS IN PATIENTS (P.) WITH IGA NEPHROPATHY (IGAN), Journal of the American Society of Nephrology, 8, 1997, pp. 440-440
Authors:
TURCO AE
BRESIN E
SOLI F
ROSSETTI S
GAMMARO L
OLDRIZZI L
MASCHIO G
PIGNATTI PF
TESSITORE N
Citation: Ae. Turco et al., MOLECULAR DNA-BASED DIAGNOSTICS IN A LARGE SERIES OF EUROPEAN FAMILIES WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD) - AN UPDATE, Journal of the American Society of Nephrology, 8, 1997, pp. 1767-1767
Authors:
ROSSETTI S
ENGLISCH S
BRESIN E
PIGNATTI PF
TURCO AE
Citation: S. Rossetti et al., DETECTION OF MUTATIONS IN HUMAN GENES BY A NEW RAPID METHOD - CLEAVAGE FRAGMENT LENGTH POLYMORPHISM ANALYSIS (CFLPA), Molecular and cellular probes, 11(2), 1997, pp. 155-160
Authors:
TURCO AE
BRESIN E
ROSSETTI S
PETERLIN B
MORANDI R
PIGNATTI PF
Citation: Ae. Turco et al., RAPID DNA-BASED PRENATAL-DIAGNOSIS BY GENETIC-LINKAGE IN 3 FAMILIES WITH ALPORTS-SYNDROME, American journal of kidney diseases, 30(2), 1997, pp. 174-179
Authors:
TURCO AE
BRESIN E
SOLI F
ROSSETTI S
GAMMARO L
MASCHIO G
PIGNATTI PF
Citation: Ae. Turco et al., GENETIC-COUNSELING, DNA-BASED INVESTIGATIONS AND PRESYMPTOMATIC MOLECULAR DIAGNOSIS IN FAMILIES WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD) AND ALPORT-SYNDROME (AS) - AN UPDATE FROM THE EXPERIENCE IN VERONA, ITALY, American journal of human genetics, 61(4), 1997, pp. 1111-1111
Authors:
TURCO AE
ROSSETTI S
BRESIN E
CORRA S
RESTAGNO G
CARBONARA A
DEPRISCO O
GAMMARO L
MASCHIO G
PIGNATTI PF
Citation: Ae. Turco et al., DETECTION OF 2 DIFFERENT NONSENSE MUTATIONS IN EXON-44 OF THE PKD1 GENE IN 2 UNRELATED ITALIAN FAMILIES WITH SEVERE AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE, Nephrology, dialysis, transplantation, 11, 1996, pp. 10-12
Authors:
BRESIN E
ROSSETTI S
ENGLISCH S
CORRA S
PIGNATTI PF
TURCO AE
Citation: E. Bresin et al., A COMMON POLYMORPHISM IN EXON-46 OF THE HUMAN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE-1 GENE (PKD1), Molecular and cellular probes, 10(6), 1996, pp. 463-465
Authors:
ROSSETTI S
BRESIN E
RESTAGNO G
CARBONARA A
CORRA S
DEPRISCO O
PIGNATTI PF
TURCO AE
Citation: S. Rossetti et al., AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD) IN AN ITALIAN FAMILY CARRYING A NOVEL NONSENSE MUTATION AND 2 MISSENSE CHANGES IN EXON-44 AND EXON-45 OF THE PKD1 GENE, American journal of medical genetics, 65(2), 1996, pp. 155-159
Authors:
TURCO AE
ROSSETTI S
BRESIN E
CORRA S
GAMMARO L
MASCHIO G
PIGNATTI PF
Citation: Ae. Turco et al., A NOVEL NONSENSE MUTATION IN THE PKD1 GENE (C3817T) IS ASSOCIATED WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD) IN A LARGE 3-GENERATION ITALIAN FAMILY, Human molecular genetics, 4(8), 1995, pp. 1331-1335
Authors:
TURCO AE
ROSSETTI S
BRESIN E
RESTAGNO G
CARBONARA A
GAMMARO L
MASCHIO G
PIGNATTI PF
Citation: Ae. Turco et al., NOVEL NONSENSE MUTATIONS IN THE PKD1 GENE IN ITALIAN FAMILIES WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD), American journal of human genetics, 57(4), 1995, pp. 1330-1330
Authors:
ANGLANI F
MURGIA A
BEDIN S
BRESIN E
BERNARDI F
CLEMENTI M
TENCONI R
Citation: F. Anglani et al., A NEW DISEASE-CAUSING MUTATION IN THE GAP-RELATED DOMAIN OF THE NF1 GENE, Human molecular genetics, 2(7), 1993, pp. 1057-1059
Authors:
MURGIA A
ANGLANI F
VINANZI C
BRESIN E
BASSO G
TENCONI R
GIANGASPERO F
PERILONGO G
ZACCHELLO F
Citation: A. Murgia et al., MUTATIONAL ANALYSIS OF THE MOST HIGHLY CONSERVED REGIONS OF THE NF1 GAP-RELATED DOMAIN, American journal of human genetics, 53(3), 1993, pp. 333-333