AAAAAA

   
Results: 1-25 | 26-31
Results: 1-25/31
NASAL POTENTIAL DIFFERENCE IN CONGENITAL BILATERAL ABSENCE OF THE VAS-DEFERENS
Authors: PRADAL U CASTELLANI C DELMARCO A MASTELLA G
Citation: U. Pradal et al., NASAL POTENTIAL DIFFERENCE IN CONGENITAL BILATERAL ABSENCE OF THE VAS-DEFERENS, American journal of respiratory and critical care medicine, 158(3), 1998, pp. 896-901
DIAGNOSIS OF CYSTIC-FIBROSIS TODAY
Authors: MASTELLA G
Citation: G. Mastella, DIAGNOSIS OF CYSTIC-FIBROSIS TODAY, Rivista italiana di pediatria, 24(2), 1998, pp. 63-66
CFTR MUTATIONS AND IVS8-5T PREVALENCE IN IDIOPATHIC CHRONIC AND ACUTERECURRENT PANCREATITIS
Authors: CASTELLANI C SGARBI D CAVALLINI G DIFRANCESCO V BOVO P FRULLONI L VAONA B BONIZZATO A BASSI C FALCONI M PEDERZOLI P MASTELLA G
Citation: C. Castellani et al., CFTR MUTATIONS AND IVS8-5T PREVALENCE IN IDIOPATHIC CHRONIC AND ACUTERECURRENT PANCREATITIS, Gastroenterology, 114(4), 1998, pp. 1811-1811
INTERNATIONAL PRACTICE PATTERNS BY AGE AND SEVERITY OF LUNG-DISEASE IN CYSTIC-FIBROSIS - DATA FROM THE EPIDEMIOLOGIC REGISTRY OF CYSTIC-FIBROSIS (ERCF)
Authors: KOCH C MCKENZIE SG KAPLOWITZ H HODSON ME HARMS HK NAVARRO J MASTELLA G
Citation: C. Koch et al., INTERNATIONAL PRACTICE PATTERNS BY AGE AND SEVERITY OF LUNG-DISEASE IN CYSTIC-FIBROSIS - DATA FROM THE EPIDEMIOLOGIC REGISTRY OF CYSTIC-FIBROSIS (ERCF), Pediatric pulmonology, 24(2), 1997, pp. 147-154
GEOGRAPHIC-DISTRIBUTION AND REGIONAL ORIGIN OF 272 CYSTIC-FIBROSIS INEUROPEAN POPULATIONS
Authors: ESTIVILL X BANCELLS C RAMOS C PIAZZA A CARBONARA A MASTELLA G BONIZZATO A CASTALDI G DALCAMO E FERRARI M GASPARINI P GUANTI G LEONI GB PIGNATTI PF RONCHETTO P SEIA M TORRICELLI F GOOSSENS M CHEVALIERPORST F BOZON D SIMONBOUY B FELDMANN D ELION J KAPLAN JC FEREC C CLAUSTRES M CLAVEL C PUCHELLE E LUNARDI J MATHIEU M SCHEFFER H HALLEY DJJ VANDENOUWELAND AMW TIJMENSEN ASLN CASALS T GIMENEZ FJ RAMOS L BENEYTO M BENITEZ J PALACIO A TUMMLER B BAUER I MEITINGER T CLAASS A LINDNER M SCHRODER E STUHRMANN M CASSIMAN J CUPPENS H COCHAUX P PONCIN J MESSIAN L BARANOV VS IVASCHENKO TE BAKAY M BAL J WITT M KANAVAKIS M TZETIS M ANTONIADI T LAVINHA J PACHECO P DUARTE A LOUREIRO P KALAYDJIEVA L ANGELICHEVA D JORDANOVA A SAVOV A EIKLID K HOLMBERG L SCHAEDEL C OZGUC M GOCMEN A ERDERN H LIECHTIGALLATI S NEMETI M FEKETE G KLAASSEN T SCHWARZ M SCHWARTZ M MACEK M MACEK M KREBSOVA A VAVROVA V KEREM B AVELIOVICH D FERAK V KADASI L KAYSEROVA H GLAVAC D RAVNIKGLAVAC M EFREMOV GD CANKIKLEIN N KERE J
Citation: X. Estivill et al., GEOGRAPHIC-DISTRIBUTION AND REGIONAL ORIGIN OF 272 CYSTIC-FIBROSIS INEUROPEAN POPULATIONS, Human mutation, 10(2), 1997, pp. 135-154
NASAL POTENTIAL DIFFERENCE IN CYSTIC-FIBROSIS PATIENTS PRESENTING BORDERLINE SWEAT TEST
Authors: DELMARCO A PRADAL U CABRINI G BONIZZATO A MASTELLA G
Citation: A. Delmarco et al., NASAL POTENTIAL DIFFERENCE IN CYSTIC-FIBROSIS PATIENTS PRESENTING BORDERLINE SWEAT TEST, The European respiratory journal, 10(5), 1997, pp. 1145-1149
ORAL CIPROFLOXACIN VS INTRAVENOUS CEFTAZIDIME PLUS TOBRAMYCIN IN PEDIATRIC CYSTIC-FIBROSIS PATIENTS - COMPARISON OF ANTIPSEUDOMONAS EFFICACY AND ASSESSMENT OF SAFETY WITH ULTRASONOGRAPHY AND MAGNETIC-RESONANCE-IMAGING
Authors: RICHARD DA NOUSIAARVANITAKIS S SOLLICH V HAMPEL BJ SOMMERAUER B SCHAAD UB SARDET A BROMME S KLODITZ E LIETZ T SCHILLE R POSSELT HG NOLL S ZIMMERMANN T BARMEIERWASMUTH H WAHN U WEBER A MAGDORF K WACKER F TROGER J LYLE M SCHMIDT A PREUSS I KRASEMANN C NIKOLAIDIS P PEONIDES A SKALIDOPOULOS S SOTIRIADIS G GYURKOVITS K BOLBAS K RIVLIN J MASTELLA G CIPOLLI M TROGU P BARRETO C LARA E EGNER J HAUPTMANN M WEDGWOOD J
Citation: Da. Richard et al., ORAL CIPROFLOXACIN VS INTRAVENOUS CEFTAZIDIME PLUS TOBRAMYCIN IN PEDIATRIC CYSTIC-FIBROSIS PATIENTS - COMPARISON OF ANTIPSEUDOMONAS EFFICACY AND ASSESSMENT OF SAFETY WITH ULTRASONOGRAPHY AND MAGNETIC-RESONANCE-IMAGING, The Pediatric infectious disease journal, 16(6), 1997, pp. 572-578
NEWBORN SCREENING STRATEGY FOR CYSTIC-FIBROSIS - A FIELD-STUDY IN AN AREA WITH HIGH ALLELIC HETEROGENEITY
Authors: CASTELLANI C BONIZZATO A CABRINI G MASTELLA G
Citation: C. Castellani et al., NEWBORN SCREENING STRATEGY FOR CYSTIC-FIBROSIS - A FIELD-STUDY IN AN AREA WITH HIGH ALLELIC HETEROGENEITY, Acta paediatrica, 86(5), 1997, pp. 497-502
FAILURE-TO-THRIVE - THE EARLIEST FEATURE OF CYSTIC-FIBROSIS IN INFANTS DIAGNOSED BY NEONATAL SCREENING
Authors: GIGLIO L CANDUSSO M DORAZIO C MASTELLA G FARAGUNA D
Citation: L. Giglio et al., FAILURE-TO-THRIVE - THE EARLIEST FEATURE OF CYSTIC-FIBROSIS IN INFANTS DIAGNOSED BY NEONATAL SCREENING, Acta paediatrica, 86(11), 1997, pp. 1162-1165
PROBLEMS RELATED TO NEONATAL SCREENING AN D MOLECULAR DIAGNOSIS OF CYSTIC-FIBROSIS
Authors: RAJNOLDI AC CORBETTA C GIUNTA A LALATTA F BENCIOLINI P BORGO G BORRONI M BRAMBATI B DANESINO C FARNETI A FERRARI M JAPICHINO L LUCCI M MARIANELLI L MASERA G MASTELLA G MIANO A NICOLINI U NOBILI R NOTARANGELO L PADOAN R PEROBELLI S ROMANO C ROMANO L SCARPA M SEIA E CABRINI G
Citation: Ac. Rajnoldi et al., PROBLEMS RELATED TO NEONATAL SCREENING AN D MOLECULAR DIAGNOSIS OF CYSTIC-FIBROSIS, Rivista italiana di pediatria, 23(5), 1997, pp. 931-935
CFTR MUTATIONS AND IVS8-5T VARIANT IN NEWBORNS WITH HYPERTRYPSINAEMIAAND NORMAL SWEAT TEST
Authors: CASTELLANI C BONIZZATO A MASTELLA G
Citation: C. Castellani et al., CFTR MUTATIONS AND IVS8-5T VARIANT IN NEWBORNS WITH HYPERTRYPSINAEMIAAND NORMAL SWEAT TEST, Journal of Medical Genetics, 34(4), 1997, pp. 297-301
GENETIC HISTORY OF CYSTIC-FIBROSIS MUTATIONS IN ITALY - I - REGIONAL DISTRIBUTION
Authors: RENDINE S CALAFELL F CAPPELLO N GAGLIARDINI R CARAMIA G RIGILLO N SILVETTI M ZANDA M MIANO A BATTISTINI F MARIANELLI L TACCETTI G DIANA MC ROMANO L ROMANO C GIUNTA A PADOAN R PIANAROLI A RAIA V DERITIS G BATTISTINI A GRZINCICH G JAPICHINO L PARDO F ANTONELLI M QUATTRUCCI S LUCIDI V CASTRO M SANTINI B CASTELLO M GUANTI G LEONI GB CAO A TOFFOLI C LUCCI E VULLO C TORRICELLI F SBERNINI F ROMEO G RONCHETTO P SEIA M ROSSI A FERRARI M CREMONESI L SALVATORE F CASTALDO G DALCAMO E MAGGIO A SANGIUOLO F DALLAPICCOLA B MACERATESI P BISCEGLIA L GASPARINI P CARBONARA A BONIZZATO A CABRINI G BOMBIERI C PIGNATTI PF BORGO G CASTELLANI C VILLANI A ARDUINO C SALVATORE D MASTELLA G PIAZZA A
Citation: S. Rendine et al., GENETIC HISTORY OF CYSTIC-FIBROSIS MUTATIONS IN ITALY - I - REGIONAL DISTRIBUTION, Annals of Human Genetics, 61, 1997, pp. 411-424
BURKHOLDERIA (PSEUDOMONAS) CEPACIA EPIDEMIOLOGY IN A CYSTIC-FIBROSIS POPULATION - A GENOME FINGER-PRINTING STUDY
Authors: GAZZOLA G AMALFITANO G TONOLLI E PERAZZOLI C PIACENTINI I MASTELLA G
Citation: G. Gazzola et al., BURKHOLDERIA (PSEUDOMONAS) CEPACIA EPIDEMIOLOGY IN A CYSTIC-FIBROSIS POPULATION - A GENOME FINGER-PRINTING STUDY, Acta paediatrica, 85(5), 1996, pp. 554-557
FIELD-INVERSION GEL-ELECTROPHORESIS ON PSEUDOMONAS-CEPACIA STRAINS ISOLATED FROM CYSTIC-FIBROSIS PATIENTS
Authors: AMALFITANO G TONOLLI E FAVARI F PERAZZOLI C CAZZOLA G MASTELLA G PIACENTINI I
Citation: G. Amalfitano et al., FIELD-INVERSION GEL-ELECTROPHORESIS ON PSEUDOMONAS-CEPACIA STRAINS ISOLATED FROM CYSTIC-FIBROSIS PATIENTS, European journal of epidemiology, 12(2), 1996, pp. 149-153
GUIDELINES FOR THE USE OF RECOMBINANT HUM AN DEOXYRIBONUCLEIC-ACID
Authors: ROMANO L PRADAL U PADOAN R ANTONELLI M DERITIS G DIANA MC GAIERO A LUCANIA A MANCA A MAPPA L MARIANELLI L MASTELLA G PARDO F PIANAROLI A
Citation: L. Romano et al., GUIDELINES FOR THE USE OF RECOMBINANT HUM AN DEOXYRIBONUCLEIC-ACID, Rivista italiana di pediatria, 22(1), 1996, pp. 113-119
DEFICIENCY OF VITAMIN-E AND VITAMIN-A IN CYSTIC-FIBROSIS IS INDEPENDENT OF PANCREATIC FUNCTION AND CURRENT ENZYME AND VITAMIN SUPPLEMENTATION
Authors: LANCELLOTTI L DORAZIO C MASTELLA G MAZZI G LIPPI U
Citation: L. Lancellotti et al., DEFICIENCY OF VITAMIN-E AND VITAMIN-A IN CYSTIC-FIBROSIS IS INDEPENDENT OF PANCREATIC FUNCTION AND CURRENT ENZYME AND VITAMIN SUPPLEMENTATION, European journal of pediatrics, 155(4), 1996, pp. 281-285
HIGH-LIPASE VERSUS LOW-LIPASE ACID-RESISTANT ENZYME PREPARATIONS IN CYSTIC-FIBROSIS - A CROSSOVER RANDOMIZED CLINICAL-TRIAL
Authors: LANCELLOTTI L CABRINI G ZANOLLA L MASTELLA G
Citation: L. Lancellotti et al., HIGH-LIPASE VERSUS LOW-LIPASE ACID-RESISTANT ENZYME PREPARATIONS IN CYSTIC-FIBROSIS - A CROSSOVER RANDOMIZED CLINICAL-TRIAL, Journal of pediatric gastroenterology and nutrition, 22(1), 1996, pp. 73-78
ESTIMATING THE INCIDENCE OF CELIAC-DISEASE WITH CAPTURE-RECAPTURE METHODS WITH 4 GEOGRAPHIC AREAS IN ITALY
Authors: CORRAO G USAI P GALATOLA G ANSALDI N MEINI A PELLI MA CASTELLUCCI G CORAZZA GR CATASSI C PANELLA C BRUSCO G CHERCHI MV BOTTARO G BASCIETTO F SPADA A GEMME G TORCHIO P PIENABARCA A ROMANO C MAGAZZU G BARDELLA MT GUANDALINI S SOLLAZZO R CATALDO F IACONO G LEONARDI C GUIDETTI CS DELLOLIO D MALORGIO E OSTINO G MASTELLA G
Citation: G. Corrao et al., ESTIMATING THE INCIDENCE OF CELIAC-DISEASE WITH CAPTURE-RECAPTURE METHODS WITH 4 GEOGRAPHIC AREAS IN ITALY, Journal of epidemiology and community health, 50(3), 1996, pp. 299-305
EFFECT OF DIFFERENT INSPIRATORY MANEUVERS ON FEV(1) IN PATIENTS WITH CYSTIC-FIBROSIS
Authors: BRAGGION C PRADAL U MASTELLA G COATES AL MILICEMILI J
Citation: C. Braggion et al., EFFECT OF DIFFERENT INSPIRATORY MANEUVERS ON FEV(1) IN PATIENTS WITH CYSTIC-FIBROSIS, Chest, 110(3), 1996, pp. 642-647
BRONCHIAL ARTERY EMBOLIZATION IN THE MANAGEMENT OF HEMOPTYSIS IN CYSTIC-FIBROSIS
Authors: CIPOLLI M PERINI S VALLETTA EA MASTELLA G
Citation: M. Cipolli et al., BRONCHIAL ARTERY EMBOLIZATION IN THE MANAGEMENT OF HEMOPTYSIS IN CYSTIC-FIBROSIS, Pediatric pulmonology, 19(6), 1995, pp. 344-347
SHORT-TERM EFFECTS OF 3 CHEST PHYSIOTHERAPY REGIMENS IN PATIENTS HOSPITALIZED FOR PULMONARY EXACERBATIONS OF CYSTIC-FIBROSIS - A CROSS-OVERRANDOMIZED STUDY
Authors: BRAGGION C CAPPELLETTI LM CORNACCHIA M ZANOLLA L MASTELLA G
Citation: C. Braggion et al., SHORT-TERM EFFECTS OF 3 CHEST PHYSIOTHERAPY REGIMENS IN PATIENTS HOSPITALIZED FOR PULMONARY EXACERBATIONS OF CYSTIC-FIBROSIS - A CROSS-OVERRANDOMIZED STUDY, Pediatric pulmonology, 19(1), 1995, pp. 16-22
RELATIONSHIPS BETWEEN GENE-MUTATIONS AND CLINICAL-FEATURES IN CYSTIC-FIBROSIS
Authors: MASTELLA G
Citation: G. Mastella, RELATIONSHIPS BETWEEN GENE-MUTATIONS AND CLINICAL-FEATURES IN CYSTIC-FIBROSIS, Pediatric pulmonology, 1995, pp. 63-65
FATAL SEPSIS FROM PSEUDOMONAS-CEPACIA IN CYSTIC-FIBROSIS
Authors: CIPOLLI M CAZZOLA GA MASTELLA G
Citation: M. Cipolli et al., FATAL SEPSIS FROM PSEUDOMONAS-CEPACIA IN CYSTIC-FIBROSIS, Rivista italiana di pediatria, 21(6), 1995, pp. 874-876
PORTAL-HYPERTENSION IN PATIENTS WITH CYSTIC-FIBROSIS AND CHRONIC LIVER-DISEASE
Authors: CIPOLLI M VALLETTA EA CAZZOLA G INASPETTATO G LORETI S MASTELLA G
Citation: M. Cipolli et al., PORTAL-HYPERTENSION IN PATIENTS WITH CYSTIC-FIBROSIS AND CHRONIC LIVER-DISEASE, Rivista italiana di pediatria, 21(1), 1995, pp. 58-62
ANALYSIS OF THE COMPLETE CODING REGION OF THE CFTR GENE IN A COHORT OF CF PATIENTS FROM NORTH-EASTERN ITALY - IDENTIFICATION OF 90-PERCENT OF THE MUTATIONS
Authors: BONIZZATO A BISCEGLIA L MARIGO C NICOLIS E BOMBIERI C CASTELLANI C BORGO G ZELANTE L MASTELLA G CABRINI G GASPARINI P PIGNATTI PF
Citation: A. Bonizzato et al., ANALYSIS OF THE COMPLETE CODING REGION OF THE CFTR GENE IN A COHORT OF CF PATIENTS FROM NORTH-EASTERN ITALY - IDENTIFICATION OF 90-PERCENT OF THE MUTATIONS, Human genetics, 95(4), 1995, pp. 397-402
Risultati: 1-25 | 26-31