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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:
Mamianetti, A
Tripodi, V
Vescina, C
Garrido, D
Vizioli, N
Carducci, C
Carreno, CA
Citation: A. Mamianetti et al., Serum bile acids and pruritus in hemodialysis patients, CLIN NEPHR, 53(3), 2000, pp. 194-198
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:
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:
Carducci, C
Birarelli, M
Nola, M
Antonozzi, I
Citation: C. Carducci et al., Automated high-performance liquid chromatographic method for the determination of homocysteine in plasma samples, J CHROMAT A, 846(1-2), 1999, pp. 93-100
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:
Chessa, L
Piane, M
Prudente, S
Carducci, C
Mazzilli, MC
Pachti, A
Negrini, M
Narducci, MG
Russo, G
Frati, L
Citation: L. Chessa et al., Molecular prenatal diagnosis of ataxia telangiectasia heterozygosity by direct mutational assays, PRENAT DIAG, 19(6), 1999, pp. 542-545
Authors:
Mardones, C
Vizioli, N
Carducci, C
Rios, A
Valcarcel, M
Citation: C. Mardones et al., Separation and determination of carnitine and acyl-carnitines by capillaryelectrophoresis with indirect UV detection, ANALYT CHIM, 382(1-2), 1999, pp. 23-31
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