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Results:
1-10
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Results: 10
Authors:
Carducci, C
Birarelli, M
Santagata, P
Leuzzi, V
Carducci, C
Antonozzi, I
Citation: C. Carducci et al., Automated high-performance liquid chromatographic method for the determination of guanidinoacetic acid in dried blood spots: a tool for early diagnosis of guanidinoacetate methyltransferase deficiency, J CHROMAT B, 755(1-2), 2001, pp. 343-348
Authors:
Carducci, C
Leuzzi, V
Carducci, C
Prudente, S
Mercuri, L
Antonozzi, I
Citation: C. Carducci et al., Two new severe mutations causing guanidinoacetate methyltransferase deficiency, MOL GEN MET, 71(4), 2000, pp. 633-638
Authors:
Leuzzi, V
Bianchi, MC
Tosetti, M
Carducci, C
Carducci, C
Antonozzi, I
Citation: V. Leuzzi et al., Clinical significance of brain phenylalanine concentration assessed by in vivo proton magnetic resonance spectroscopy in phenylketonuria, J INH MET D, 23(6), 2000, pp. 563-570
Authors:
Leuzzi, V
Seri, S
Cerquiglini, A
Carducci, C
Carducci, C
Antonozzi, I
Citation: V. Leuzzi et al., Derangement of the dopaminergic system in phenylketonuria: Study of the event-related potential (P300), J INH MET D, 23(4), 2000, pp. 317-320
Authors:
Rizzo, C
Bertini, E
Piemonte, F
Leuzzi, V
Sabetta, G
Federici, G
Luchetti, A
Dionisi-Vici, C
Citation: C. Rizzo et al., Oxidative abnormalities in Menkes disease, J INH MET D, 23(4), 2000, pp. 349-351
Authors:
Leuzzi, V
Bianchi, MC
Tosetti, M
Carducci, C
Cerquiglini, A
Cioni, G
Antonozzi, I
Citation: V. Leuzzi et al., Brain creatine depletion: Guanidinoacetate methyltransferase deficiency (improving with creatine supplementation), NEUROLOGY, 55(9), 2000, pp. 1407-1409
Authors:
Leuzzi, V
Rinna, A
Gallucci, M
Di Capua, M
Dionisi-Vici, C
Longo, D
Bertini, E
Citation: V. Leuzzi et al., Ataxia, deafness, leukodystrophy: Inherited disorder of the white matter in three related patients, NEUROLOGY, 54(12), 2000, pp. 2325-2328
Authors:
Dionisi-Vici, C
Hoffmann, GF
Leuzzi, V
Hoffken, H
Brautigam, C
Rizzo, C
Steebergen-Spanjers, GCH
Smeitink, JAM
Wevers, RA
Citation: C. Dionisi-vici et al., Tyrosine hydroxylase deficiency with severe clinical course: Clinical and biochemical investigations and optimization of therapy, J PEDIAT, 136(4), 2000, pp. 560-562
Authors:
Carelli, V
Ghelli, A
Bucchi, L
Montagna, P
De Negri, A
Leuzzi, V
Carducci, C
Lenaz, G
Lugaresi, E
Degli Esposti, M
Citation: V. Carelli et al., Biochemical features of mtDNA 14484 (ND6/M64V) point mutation associated with Leber's hereditary optic neuropathy, ANN NEUROL, 45(3), 1999, pp. 320-328
Authors:
Leuzzi, V
Lyon, G
Cilio, MR
Pedespan, JM
Fontan, D
Chateil, JF
Vital, A
Citation: V. Leuzzi et al., Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases, J NE NE PSY, 66(3), 1999, pp. 407-408
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