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Results: 1-8 |
Results: 8
DIAGNOSIS, CLASSIFICATION, BASIS OF TREAT MENT OF HYPERPHENYLALANINEMIAS
Authors: ROMANO C BURRONI M CACCIARI E CERONE R CORBETTA C LILLIU F BALSAMO A CARDILLO A CARNEVALE F CARUSO U CIATTI R CIONI M DOTTI L IMPELLIZZERI A LELLI A LEUZZI V PAGLIARDINI S PIAZZI S PRINCIPI R SALARDI S SCHIAFFINO MC ALOISI R ALTAMURA A BIASUCCI G BURLINA AB COTUGNO G FABIANO F GHIRRI P GIOVANNINI M MELI C MOSTARDINI R MUSARO MA PAOLILLO L PERUZZI L PIGNERO A PULITI MT RIVA E SORTINO C SPADA M TERRANOVA D ZAMMARCHI E
Citation: C. Romano et al., DIAGNOSIS, CLASSIFICATION, BASIS OF TREAT MENT OF HYPERPHENYLALANINEMIAS, Rivista italiana di pediatria, 23(6), 1997, pp. 1040-1044
CHRONIC HEPATITIS-C VIRUS-INFECTION - PREDICTIVE VALUE OF GENOTYPE ONDISEASE PROGRESSION
Authors: FENOGLIO LM MONASTEROLO G FRUTTERO M PEANO GM CARNEVALE F WULHFARD K SABIDUSSI A BIARESE V
Citation: Lm. Fenoglio et al., CHRONIC HEPATITIS-C VIRUS-INFECTION - PREDICTIVE VALUE OF GENOTYPE ONDISEASE PROGRESSION, Hepatology, 26(4), 1997, pp. 1506-1506
CHRONIC HEPATITIS-C VIRUS-INFECTION - PREDICTIVE VALUE OF GENOTYPE ONDISEASE PROGRESSION
Authors: FENOGLIO LM MONASTEROLO G FRUTTERO M PEANO GM CARNEVALE F WULHFARD K SABIDUSSI A BIARESE V
Citation: Lm. Fenoglio et al., CHRONIC HEPATITIS-C VIRUS-INFECTION - PREDICTIVE VALUE OF GENOTYPE ONDISEASE PROGRESSION, Gastroenterology, 112(4), 1997, pp. 1263-1263
RESPIRATORY-CHAIN AND PYRUVATE METABOLISM DEFECTS - ITALIAN COLLABORATIVE SURVEY ON 72 PATIENTS
Authors: CARUSO U ADAMI A BERTINI E BURLINA AB CARNEVALE F CERONE R DIONISIVICI C GIORDANO G LEUZZI E PARENTI G SAVASTA S UZIEL G ZEVIANI M
Citation: U. Caruso et al., RESPIRATORY-CHAIN AND PYRUVATE METABOLISM DEFECTS - ITALIAN COLLABORATIVE SURVEY ON 72 PATIENTS, Journal of inherited metabolic disease, 19(2), 1996, pp. 143-148
BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY IN 2 MALE INFANTS - 3RD FAMILY REPORT
Authors: PAPADIA F POLLICE L NATALE B BELLANTUONO R CONTI P CARNEVALE F
Citation: F. Papadia et al., BILIARY MALFORMATION WITH RENAL TUBULAR INSUFFICIENCY IN 2 MALE INFANTS - 3RD FAMILY REPORT, Clinical genetics, 49(5), 1996, pp. 267-270
CHARACTERIZATION OF PHENYLKETONURIA ALLELES IN THE ITALIAN POPULATION
Authors: DIANZANI I GIANNATTASIO S DESANCTIS L ALLIAUDI C LATTANZIO P VICI CD BURLINA A BURRONI M SEBASTIO G CARNEVALE F GUZZETTA V MARRA E CAMASCHELLA C PONZONE A
Citation: I. Dianzani et al., CHARACTERIZATION OF PHENYLKETONURIA ALLELES IN THE ITALIAN POPULATION, European journal of human genetics, 3(5), 1995, pp. 294-302
FISH ANALYSIS IN PRADER-WILLI AND ANGELMAN SYNDROME PATIENTS
Authors: BETTIO D RIZZI N GIARDINO D GRUGNI G BRISCIOLI V SELICORNI A CARNEVALE F LARIZZA L
Citation: D. Bettio et al., FISH ANALYSIS IN PRADER-WILLI AND ANGELMAN SYNDROME PATIENTS, American journal of medical genetics, 56(2), 1995, pp. 224-228
A NEW GENIC MUTATION IN A FAMILY AFFECTED BY X-LINKED NEPHROGENIC DIABETES-INSIPIDUS (NDI) AND INTRACRANIAL CALCIFICATIONS (IC)
Authors: BELLANTUONO R GIORDANO M SIMONETTI S PAPADIA F CARNEVALE F BICHET DG CARINGELLA DA
Citation: R. Bellantuono et al., A NEW GENIC MUTATION IN A FAMILY AFFECTED BY X-LINKED NEPHROGENIC DIABETES-INSIPIDUS (NDI) AND INTRACRANIAL CALCIFICATIONS (IC), Kidney international, 47(1), 1995, pp. 364-364
Risultati: 1-8 |