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Results: 1-25 | 26-50 | 51-57
Results: 26-50/57

Authors: CETTA F CIVITELLI S PACCHIAROTTI MC LORE F RENIERI A PETRACCI M GIUBBOLINI M BALDI C
Citation: F. Cetta et al., FOLLICULAR AND PAPILLARY CARCINOMAS OF THE THYROID-ASSOCIATED WITH FAMILIAL ADENOMATOUS POLYPOSIS ARE LIKELY TO HAVE EARLY AND INTERMEDIATECOMMON PREMALIGNANT CHANGES, Gastroenterology, 110(4), 1996, pp. 501-501

Authors: RENIERI A BRUTTINI M GALLI L ZANELLI P NERI T ROSSETTI S TURCO A HEISKARI N ZHOU J GUSMANO R MASSELLA L BANFI G SCOLARI F SESSA A RIZZONI G TRYGGVASON K PIGNATTI PF SAVI M BALLABIO A DEMARCHI M
Citation: A. Renieri et al., X-LINKED ALPORT-SYNDROME - AN SSCP-BASED MUTATION SURVEY OVER ALL 51 EXONS OF THE COL4A5 GENE, American journal of human genetics, 58(6), 1996, pp. 1192-1204

Authors: BASSI MT SCHIAFFINO MV RENIERI A DENIGRIS F GALLI L BRUTTINI M GEBBIA M BERGEN AAB LEWIS RA BALLABIO A
Citation: Mt. Bassi et al., CLONING OF THE GENE FOR OCULAR ALBINISM TYPE-1 FROM THE DISTAL SHORT ARM OF THE X-CHROMOSOME, Nature genetics, 10(1), 1995, pp. 13-19

Authors: SCHIAFFINO MV BASSI MT RUGARLI EI RENIERI A GALLI L BALLABIO A
Citation: Mv. Schiaffino et al., CLONING OF A HUMAN HOMOLOG OF THE XENOPUS-LAEVIS APX GENE FROM THE OCULAR ALBINISM TYPE-1 CRITICAL REGION, Human molecular genetics, 4(3), 1995, pp. 373-382

Authors: SCHIAFFINO MV BASSI MT GALLI L RENIERI A BRUTTINI M DENIGRIS F BERGEN AAB CHARLES SJ YATES JRW MEINDL A LEWIS RA KING RA BALLABIO A
Citation: Mv. Schiaffino et al., ANALYSIS OF THE OA1 GENE REVEALS MUTATIONS IN ONLY 1 3 OF PATIENTS WITH X-LINKED OCULAR ALBINISM/, Human molecular genetics, 4(12), 1995, pp. 2319-2325

Authors: MASSELLA L DENIGRIS A FARAGGIANA T DEBLASIIS R BARSOTTI P RENIERI A NERI T TURCO AE DEMARCHI M RIZZONI G
Citation: L. Massella et al., ALPORT SYNDROME - NEW GENETIC PERSPECTIVE S ON CLINICAL AND HISTOLOGICAL DIAGNOSIS, Rivista italiana di pediatria, 21, 1995, pp. 80-85

Authors: DATTOLI G GIANNESSI L OTTAVIANI PL RENIERI A
Citation: G. Dattoli et al., A MODEL FOR THE SATURATION OF A STORAGE-RING FREE-ELECTRON LASER, Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 365(2-3), 1995, pp. 559-563

Authors: GIOVENALE E CIOCCI F DORIA A GALLERANO GP KIMMITT MF MESSINA G RAIMONDI P RENIERI A SPASSOVSKY I
Citation: E. Giovenale et al., UPGRADE OF THE ENEA COMPACT FEL IN THE SUB-MM REGION, Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 358(1-3), 1995, pp. 22-23

Authors: DATTOLI G GIANNESSI L RENIERI A
Citation: G. Dattoli et al., THEORY OF THE LONGITUDINAL DYNAMICS OF A STORAGE-RING FEL, Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 358(1-3), 1995, pp. 338-340

Authors: RENIERI A GALLI L GRILLO A BRUTTINI M NERI T ZANELLI P RIZZONI G MASSELLA L SESSA A MERONI M PERATONER L RIEGLER P SCOLARI F MILETI M GIANI M COSSU M SAVI M BALLABIO A DEMARCHI M
Citation: A. Renieri et al., MAJOR COL4A5 GENE REARRANGEMENTS IN PATIENTS WITH JUVENILE TYPE ALPORT SYNDROME, American journal of medical genetics, 59(3), 1995, pp. 380-385

Authors: PIETRUCCI A MERONI M CAROZZI S TAZZARI S TARELLI LT GIORDANO F RENIERI A DEMARCHI M VALENTE U SESSA A
Citation: A. Pietrucci et al., CAN ASYMPTOMATIC WOMEN CARRIERS OF THE ALPORT SYNDROME GENE BE ACCEPTED AS LIVING KIDNEY DONORS, Kidney international, 47(1), 1995, pp. 371-371

Authors: SESSA A PIETRUCCI A CAROZZI S TARELLI LT TAZZARI S GIORDANO F MERONI M BATTINI G VALENTE U RENIERI A DEMARCHI M
Citation: A. Sessa et al., RENAL-TRANSPLANTATION FROM LIVING DONOR PARENTS IN 2 BROTHERS WITH ALPORT SYNDROME - CAN ASYMPTOMATIC FEMALE CARRIERS OF THE ALPORT GENE BEACCEPTED AS KIDNEY DONORS, Nephron, 70(1), 1995, pp. 106-109

Authors: TURCO AE ROSSETTI S BIASI MO RIZZONI G MASSELLA L SAARINEN NH RENIERI A PIGNATTI PF DEMARCHI M
Citation: Ae. Turco et al., A NOVEL MISSENSE MUTATION IN EXON-3 OF THE COL4A5 GENE ASSOCIATED WITH LATE-ONSET ALPORT SYNDROME, Clinical genetics, 48(5), 1995, pp. 261-263

Authors: BASSI MT SCHIAFFINO MV RENIERI A DENIGRIS F GALLI L BRUTTINI M BERGEN AAB LEWIS RA YATES J MEITINGER T BALLABIO A
Citation: Mt. Bassi et al., GENOMIC STRUCTURE AND MUTATION ANALYSIS OF THE OCULAR ALBINISM TYPE-1(OA1) GENE, American journal of human genetics, 57(4), 1995, pp. 25-25

Authors: RENIERI A BRUTTINI M GALLI L NERI T ZANELLI P TURCO A ROSSETTI S MERONI M SESSA A MASSELLA L RIZZONI G PIGNATTI GF SAVI M BALLABIO A DEMARCHI M
Citation: A. Renieri et al., MUTATION SCANNING OF THE ENTIRE COL4A5 CODING SEQUENCE IN ALPORT SYNDROME AND GENOTYPE-PHENOTYPE CORRELATION, American journal of human genetics, 57(4), 1995, pp. 35-35

Authors: RENIERI A BASSI MT GALLI L ZHOU J GIANI M DEMARCHI M BALLABIO A
Citation: A. Renieri et al., DELETION SPANNING THE 5' ENDS OF BOTH THE COL4A5 AND COL4A6 GENES IN A PATIENT WITH ALPORTS-SYNDROME AND LEIOMYOMATOSIS, Human mutation, 4(3), 1994, pp. 195-198

Authors: PEISSEL B ROSSETTI S RENIERI A GALLI L DEMARCHI M BATTINI G MERONI M SESSA A SCHIAVANO S PIGNATTI PF TURCO AE
Citation: B. Peissel et al., A NOVEL FRAMESHIFT DELETION IN TYPE-IV COLLAGEN ALPHA-5 GENE IN A JUVENILE-TYPE ALPORT SYNDROME PATIENT - AN ADENINE DELETION (2940 2943 DEL A) IN EXON 34 OF COL4A5/, Human mutation, 3(4), 1994, pp. 386-390

Authors: MERONI M CAROZZI S PIETRUCCI A TAZZARI S TARELLI LT RENIERI A SESSA A
Citation: M. Meroni et al., RENAL-TRANSPLANTATION FROM LIVING DONOR PARENTS IN 2 BROTHERS WITH ALPORT SYNDROME, Journal of the American Society of Nephrology, 5(3), 1994, pp. 649-649

Authors: MASSELLA L MAZZUCCO G BARSOTTI P FARAGGIANA T RENIERI A DENIGRIS A GALLI L SERI M NERI T TURCO A MERONI M SESSA A DEMARCHI M MONGA G RIZZONI G
Citation: L. Massella et al., CLINICAL AND MORPHOLOGICAL FEATURES OF 25 FAMILIES WITH ALPORT SYNDROME (AS) IN WHICH A COL-4A5 GENE MUTATION WAS IDENTIFIED, Journal of the American Society of Nephrology, 5(3), 1994, pp. 649-649

Authors: RENIERI A GALLI L ZHOU J BALLABIO A DEMARCHI M
Citation: A. Renieri et al., A BG II POLYMORPHISM IN THE COL4A6 GENE, Human molecular genetics, 3(10), 1994, pp. 1914-1914

Authors: RENIERI A GALLI L DEMARCHI M VOLTI SL MOLLICA F LUPO A MASCHIO G PEISSEL B ROSSETTI S PIGNATTI P TURCO AE
Citation: A. Renieri et al., SINGLE-BASE PAIR DELETIONS IN EXONS 39 AND 42 OF THE COL4A5 GENE IN ALPORT SYNDROME, Human molecular genetics, 3(1), 1994, pp. 201-202

Authors: MASSELLA L RIZZONI G DEBLASIS R BARSOTTI P FARAGGIANA T RENIERI A SERI M GALLI L DEMARCHI M
Citation: L. Massella et al., DE-NOVO COL4A5 GENE-MUTATIONS IN ALPORTS-SYNDROME, Nephrology, dialysis, transplantation, 9(10), 1994, pp. 1408-1411

Authors: BARBAGELATA L CUROTTO S GRATTAROLA M GUALCO G ROSATELLI F CIOCCI F RENIERI A
Citation: L. Barbagelata et al., MAGNETIC MEASUREMENTS OF A HYBRID PERMANENT-MAGNET UNDULATOR FOR THE LISA-SURF IR FEL EXPERIMENT, Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 341(1-3), 1994, pp. 10200130-10200131

Authors: CASTELLANO M FERRARIO M MINESTRINI M PATTERI P TAZZIOLI F CEVENINI F CIOCCI F DATTOLI G DIPACE A GALLERANO GP RENIERI A SABIA E CATANI L TAZZARI S
Citation: M. Castellano et al., STATUS OF THE COMMISSIONING OF THE SC LINAC LISA FOR SURF FEL EXPERIMENT, Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 341(1-3), 1994, pp. 10219043-10219044

Authors: CIOCCI F DELLAVALLE F DORIA A GALLERANO GP GIANNESSI L GIOVENALE E HAUSER P KOTTMANN F MESSINA G MILOTTI E PETITJEAN C PICARDI L RENIERI A RIZZO C RONSIVALLE C SIMONS LM TAQQU D VACCHI A VIGNATI A ZAVATTINI E
Citation: F. Ciocci et al., COMPACT WAVE-GUIDE FEL FOR SPECTROSCOPIC MEASUREMENTS IN MUONIC HYDROGEN, Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 341(1-3), 1994, pp. 10219060-10219061
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