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Results: 1-13 |
Results: 13

Authors: DIONISIVICI C DEFELICE L ELHACHEM M BOTTERO S RIZZO C PAOLONI A GOFFREDO B SABETTA G CANIGLIA M
Citation: C. Dionisivici et al., INTRAVENOUS IMMUNE GLOBULIN IN LYSINURIC PROTEIN INTOLERANCE, Journal of inherited metabolic disease, 21(2), 1998, pp. 95-102

Authors: DIONISIVICI C RUITENBEEK W FARIELLO G BENTLAGE H WANDERS RJA SCHAGGER H BOSMAN C PIANTADOSI C SABETTA G BERTINI E
Citation: C. Dionisivici et al., NEW FAMILIAL MITOCHONDRIAL ENCEPHALOPATHY WITH MACROCEPHALY, CARDIOMYOPATHY, AND COMPLEX-I DEFICIENCY, Annals of neurology, 42(4), 1997, pp. 661-665

Authors: FARIELLO G DIONISIVICI C ORAZI C MALENA S BARTULI A SCHINGO P CARNEVALE E SAPONARA I SABETTA G
Citation: G. Fariello et al., CRANIAL ULTRASONOGRAPHY IN MAPLE-SYRUP-URINE-DISEASE, American journal of neuroradiology, 17(2), 1996, pp. 311-315

Authors: DIONISIVICI C GARAVAGLIA B BURLINA AB BERTINI E SAPONARA I SABETTA G TARONI F
Citation: C. Dionisivici et al., HYPOPARATHYROIDISM IN MITOCHONDRIAL TRIFUNCTIONAL PROTEIN-DEFICIENCY, The Journal of pediatrics, 129(1), 1996, pp. 159-162

Authors: ANDRIA G GATTI R BALLABIO A MASTROIACOVO P BURGIO R RUBINO A CAO A SABETTA G DALLAPICCOLA B DIDONATO S
Citation: G. Andria et al., TREATMENT OF INTRATHECAL INFUSION OF WHIT E BLOOD-CELLS IN GENETIC-DISEASES, Rivista italiana di pediatria, 21(6), 1995, pp. 901-902

Authors: BARTULI A PICCA S VICI CD GRECO M DELLOSTROLOGO L BURLINA AB SABETTA G RIZZONI G
Citation: A. Bartuli et al., ROLE OF DIALYSIS IN THE TREATMENT OF CHIL DREN WITH ACUTE DECOMPENSATION IN CONGENITAL METABOLIC DISORDERS, Rivista italiana di pediatria, 21, 1995, pp. 93-98

Authors: DIONISIVICI C GARAVAGLIA B BURLINA A BERTINI E WANDERS RJA HASHIMOTO T SABETTA G INVERNIZZI F TARONI F DIDONATO S
Citation: C. Dionisivici et al., MITOCHONDRIAL TRIFUNCTIONAL PROTEIN-DEFICIENCY - CLINICAL AND BIOCHEMICAL FINDINGS IN POUR PATIENTS, Annals of neurology, 38(3), 1995, pp. 544-544

Authors: BURLINA AB DIONISIVICI C PIOVAN S SAPONARA I BARTULI A SABETTA G ZACCHELLO F
Citation: Ab. Burlina et al., ACUTE-PANCREATITIS IN PROPIONIC ACIDEMIA, Journal of inherited metabolic disease, 18(2), 1995, pp. 169-172

Authors: DIONISIVICI C SAPONARA I BURLINA AB GARAVAGLIA B DIDONATO S PICCA S BERTINI E SABETTA G
Citation: C. Dionisivici et al., MITOCHONDRIAL TRIFUNCTIONAL PROTEIN-DEFICIENCY AND HYPOPARATHYROIDISM, Pediatric research, 37(4), 1995, pp. 147-147

Authors: DIONSIVICI C GARAVAGLIA B BARTULI A INVERNIZZI F DIDONATO S SABETTA G KAHLER SG MILLINGTON DS
Citation: C. Dionsivici et al., CARNITINE ACYLCARNITINE TRANSLOCASE DEFICIENCY - BENIGN COURSE WITHOUT CARDIAC INVOLVEMENT, Pediatric research, 37(4), 1995, pp. 147-147

Authors: DIONISIVICI C BERTINI E SABETTA G SAPONARA I SERVIDEI S BENNETT MJ BURLINA AB
Citation: C. Dionisivici et al., A NOVEL MITOCHONDRIAL ENCEPHALOPATHY OCULOPATHY CARDIOPATHY MYOPATHY WITH ABNORMAL ORGANIC ACIDURIA AND COMBINED COMPLEX-1 AND COMPLEX-IV RESPIRATORY-CHAIN ENZYME DEFICIENCY, Pediatric research, 35(4), 1994, pp. 10000201-10000201

Authors: BURLINA AB DIONISIVICI C BENNETT MJ GIBSON KM SERVIDEI S BERTINI E HALE DE SCHMIDTSOMMERFELD E SABETTA G ZACCHELLO F RINALDO P
Citation: Ab. Burlina et al., A NEW SYNDROME WITH ETHYLMALONIC ACIDURIA AND NORMAL FATTY-ACID OXIDATION IN FIBROBLASTS, The Journal of pediatrics, 124(1), 1994, pp. 79-86

Authors: GENUARDI M DIONISIVICI C SABETTA G MIGNOZZI M RIZZONI G COTUGNO G NERI MEM
Citation: M. Genuardi et al., CEREBRO-RENO-DIGITAL (MECKEL-LIKE) SYNDROME WITH DANDY-WALKER MALFORMATION, CYSTIC KIDNEYS, HEPATIC-FIBROSIS, AND POLYDACTYLY, American journal of medical genetics, 47(1), 1993, pp. 50-53
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