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Results:
1-19
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Results: 19
Authors:
PEZZI PP
DENEGRI AM
SADUN F
CARELLI V
LEUZZI V
Citation: Pp. Pezzi et al., CHILDHOOD LEBER HEREDITARY OPTIC NEUROPATHY (ND1 3460) WITH VISUAL RECOVERY/, Pediatric neurology, 19(4), 1998, pp. 308-312
Authors:
LEUZZI V
RINNA A
GALLUCCI M
DIONISIVICI C
BERTINI E
Citation: V. Leuzzi et al., ATAXIA-DEAFNESS-LEUKODYSTROPHY - A NEW INHERITED DISORDER OF THE WHITE-MATTER, Annals of neurology, 44(3), 1998, pp. 37-37
Authors:
LEUZZI V
RINALDUZZI S
CHIAROTTI F
GARZIA P
TRASIMENI G
ACCORNERO N
Citation: V. Leuzzi et al., SUBCLINICAL VISUAL IMPAIRMENT IN PHENYLKETONURIA - A NEUROPHYSIOLOGICAL STUDY (VEP-P) WITH CLINICAL, BIOCHEMICAL, AND NEURORADIOLOGICAL (MRI) CORRELATIONS, Journal of inherited metabolic disease, 21(4), 1998, pp. 351-364
Authors:
CARELLI V
GHELLI A
CEVOLI S
CORTELLI P
LUGARESI E
BARUZZI A
LEUZZI V
DEGLIESPOSTI M
BARBONI P
MONTAGNA P
Citation: V. Carelli et al., IDEBENONE THERAPY IN LEBERS HEREDITARY OPTIC NEUROPATHY - REPORT OF 6CASES, Neurology, 50(4), 1998, pp. 2002-2002
Authors:
BARBETTI F
FIDONE F
BONFANTI R
PRISCO F
CARDUCCI C
ROMANO V
LEUZZI V
MESCHI F
Citation: F. Barbetti et al., INCREASED AMINO-ACID URINARY-EXCRETION AND RENAL GLYCOSURIA IN A FAMILY WITH A MUTATION (Y122C) IN THE HNF1-ALPHA GENE (MODY-3), Diabetes, 47, 1998, pp. 1532-1532
Authors:
LEUZZI V
FOIS D
CARDUCCI C
ANTONOZZI I
TRASIMENI G
Citation: V. Leuzzi et al., NEUROPSYCHOLOGICAL AND NEURORADIOLOGICAL (MRI) VARIATIONS DURING PHENYLALANINE LOAD - PROTECTIVE EFFECT OF VALINE, LEUCINE, AND ISOLEUCINE SUPPLEMENTATION, Journal of child neurology, 12(5), 1997, pp. 338-340
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
Authors:
CARELLI V
GHELLI A
RATTA M
BACCHILEGA E
SANGIORGI S
MANCINI R
LEUZZI V
CORTELLI P
MONTAGNA P
LUGARESI E
ESPOSTI MD
Citation: V. Carelli et al., LEBERS HEREDITARY OPTIC NEUROPATHY - BIOCHEMICAL EFFECT OF 11778 ND4 AND 3460/ND1 MUTATIONS AND CORRELATION WITH THE MITOCHONDRIAL GENOTYPE/, Neurology, 48(6), 1997, pp. 1623-1632
Authors:
TORRONI A
PETROZZI M
DURBANO L
SELLITTO D
ZEVIANI M
CARRARA F
CARDUCCI C
LEUZZI V
CARELLI V
BARBONI P
DENEGRI A
SCOZZARI R
Citation: A. Torroni et al., HAPLOTYPE AND PHYLOGENETIC ANALYSES SUGGEST THAT ONE EUROPEAN-SPECIFIC MTDNA BACKGROUND PLAYS A ROLE IN THE EXPRESSION OF LEBER HEREDITARY OPTIC NEUROPATHY BY INCREASING THE PENETRANCE OF THE PRIMARY MUTATION-11778 AND MUTATION-14484, American journal of human genetics, 60(5), 1997, pp. 1107-1121
Authors:
LEUZZI V
CARDUCCI C
LANZA M
SALVETTI M
RISTORI G
DIGIOVANNI S
TORRONI A
Citation: V. Leuzzi et al., LHON MUTATIONS IN ITALIAN PATIENTS AFFECTED BY MULTIPLE-SCLEROSIS, Acta neurologica Scandinavica, 96(3), 1997, pp. 145-148
Authors:
CARDUCCI C
BIRARELLI M
LEUZZI V
SANTAGATA G
SERAFINI P
ANTONOZZI I
Citation: C. Carducci et al., AUTOMATED-METHOD FOR THE MEASUREMENT OF AMINO-ACIDS IN URINE BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY, Journal of chromatography, 729(1-2), 1996, pp. 173-180
Authors:
DEGIORGIS GF
NONNIS E
CROCIONI F
GREGORI P
ROSINI MP
LEUZZI V
LOIZZO A
Citation: Gf. Degiorgis et al., EVOLUTION OF DAYTIME QUIET SLEEP COMPONENTS IN EARLY TREATED PHENYLKETONURIC INFANTS, Brain & development, 18(3), 1996, pp. 201-206
Authors:
LEUZZI V
DENEGRI AM
CARDUCCI CA
SANGIORGI S
CARELLI V
PIVETTIPEZZI P
Citation: V. Leuzzi et al., BIOCHEMICAL-STUDY OF ND1 3460 LEBER OPTIC NEUROPATHY WITH VISUAL RECOVERY/, Annals of neurology, 40(2), 1996, pp. 55-55
Authors:
CARDUCCI C
DENEGRI AM
LEUZZI V
TERREGINO C
TORELLA M
PEZZI PP
ANTONOZZI I
Citation: C. Carducci et al., SCREENING OF MTDNA MUTATIONS IN ITALIAN LHON PEDIGREES, Journal of inherited metabolic disease, 19(2), 1996, pp. 127-129
Authors:
LEUZZI V
TRASIMENI G
GUALDI GF
ANTONOZZI I
Citation: V. Leuzzi et al., BIOCHEMICAL, CLINICAL AND NEURORADIOLOGICAL (MRI) CORRELATIONS IN LATE-DETECTED PKU PATIENTS, Journal of inherited metabolic disease, 18(5), 1995, pp. 624-634
Authors:
FIESCHI C
GASPERINI C
RISTORI G
BASTIANELLO S
GIRMENIA F
LEUZZI V
BUTTINELLI C
RASURA M
Citation: C. Fieschi et al., PATIENTS WITH CLINICALLY DEFINITE MULTIPLE-SCLEROSIS, WHITE-MATTER ABNORMALITIES ON MRI, AND NORMAL CSF - IF NOT MULTIPLE-SCLEROSIS, WHAT IS IT, Journal of Neurology, Neurosurgery and Psychiatry, 58(2), 1995, pp. 255-256
Authors:
LEUZZI V
CARDONA F
ANTONOZZI I
LOIZZO A
Citation: V. Leuzzi et al., VISUAL, AUDITORY, AND SOMATOSENSORIAL EVOKED-POTENTIALS IN EARLY AND LATE TREATED ADOLESCENTS WITH PHENYLKETONURIA, Journal of clinical neurophysiology, 11(6), 1994, pp. 602-606
Authors:
LEUZZI V
ELLI R
ANTONELLI A
CHESSA L
CARDONA F
MARCUCCI L
PETRINELLI P
Citation: V. Leuzzi et al., NEUROLOGICAL AND CYTOGENETIC STUDY IN EARLY-ONSET ATAXIA-TELANGIECTASIA PATIENTS, European journal of pediatrics, 152(7), 1993, pp. 609-612
Authors:
LEUZZI V
GUALDI GF
FABBRIZI F
TRASIMENI G
DIBIASI C
ANTONOZZI I
Citation: V. Leuzzi et al., NEURORADIOLOGICAL (MRI) ABNORMALITIES IN PHENYLKETONURIC SUBJECTS - CLINICAL AND BIOCHEMICAL CORRELATIONS, Neuropediatrics, 24(6), 1993, pp. 302-306
Risultati:
1-19
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