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La ricerca find articoli where authors phrase all words ' BRESIN E' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 14 riferimenti
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    1. TURCO AE; ROSSETTI S; BRESIN E; ENGLISCH S; CORRA S; PIGNATTI PF
      3 NOVEL MUTATIONS OF THE PKD1 GENE IN ITALIAN FAMILIES WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE

      Human mutation
    2. LUPO A; MARCANTONI C; OLDRIZZI L; BRESIN E; MASCHIO G
      ACE GENE POLYMORPHISM AND CLINICAL AND MORPHOLOGICAL CORRELATIONS IN PATIENTS (P.) WITH IGA NEPHROPATHY (IGAN)

      Journal of the American Society of Nephrology
    3. TURCO AE; BRESIN E; SOLI F; ROSSETTI S; GAMMARO L; OLDRIZZI L; MASCHIO G; PIGNATTI PF; TESSITORE N
      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
    4. ROSSETTI S; ENGLISCH S; BRESIN E; PIGNATTI PF; TURCO AE
      DETECTION OF MUTATIONS IN HUMAN GENES BY A NEW RAPID METHOD - CLEAVAGE FRAGMENT LENGTH POLYMORPHISM ANALYSIS (CFLPA)

      Molecular and cellular probes
    5. TURCO AE; BRESIN E; ROSSETTI S; PETERLIN B; MORANDI R; PIGNATTI PF
      RAPID DNA-BASED PRENATAL-DIAGNOSIS BY GENETIC-LINKAGE IN 3 FAMILIES WITH ALPORTS-SYNDROME

      American journal of kidney diseases
    6. TURCO AE; BRESIN E; SOLI F; ROSSETTI S; GAMMARO L; MASCHIO G; PIGNATTI PF
      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
    7. TURCO AE; ROSSETTI S; BRESIN E; CORRA S; RESTAGNO G; CARBONARA A; DEPRISCO O; GAMMARO L; MASCHIO G; PIGNATTI PF
      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
    8. BRESIN E; ROSSETTI S; ENGLISCH S; CORRA S; PIGNATTI PF; TURCO AE
      A COMMON POLYMORPHISM IN EXON-46 OF THE HUMAN AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE-1 GENE (PKD1)

      Molecular and cellular probes
    9. ROSSETTI S; BRESIN E; RESTAGNO G; CARBONARA A; CORRA S; DEPRISCO O; PIGNATTI PF; TURCO AE
      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
    10. TURCO AE; ROSSETTI S; BRESIN E; CORRA S; GAMMARO L; MASCHIO G; PIGNATTI PF
      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
    11. TURCO AE; ROSSETTI S; BRESIN E; CORRA S
      ERRONEOUS GENETIC RISK ASSESSMENT OF ALPORT SYNDROME

      Lancet
    12. TURCO AE; ROSSETTI S; BRESIN E; RESTAGNO G; CARBONARA A; GAMMARO L; MASCHIO G; PIGNATTI PF
      NOVEL NONSENSE MUTATIONS IN THE PKD1 GENE IN ITALIAN FAMILIES WITH AUTOSOMAL-DOMINANT POLYCYSTIC KIDNEY-DISEASE (ADPKD)

      American journal of human genetics
    13. ANGLANI F; MURGIA A; BEDIN S; BRESIN E; BERNARDI F; CLEMENTI M; TENCONI R
      A NEW DISEASE-CAUSING MUTATION IN THE GAP-RELATED DOMAIN OF THE NF1 GENE

      Human molecular genetics
    14. MURGIA A; ANGLANI F; VINANZI C; BRESIN E; BASSO G; TENCONI R; GIANGASPERO F; PERILONGO G; ZACCHELLO F
      MUTATIONAL ANALYSIS OF THE MOST HIGHLY CONSERVED REGIONS OF THE NF1 GAP-RELATED DOMAIN

      American journal of human genetics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 15/01/21 alle ore 18:51:10