Leuzzi V - Search Results

1

Predictability and inconsistencies in the cognitive outcome of early treated PKU patients.

Manti F, Nardecchia F, Paci S, Chiarotti F, Carducci C, Carducci C, Dalmazzone S, Cefalo G, Salvatici E, Banderali G, Leuzzi V. Manti F, et al. Among authors: leuzzi v. J Inherit Metab Dis. 2017 Nov;40(6):793-799. doi: 10.1007/s10545-017-0082-y. Epub 2017 Aug 23. J Inherit Metab Dis. 2017. PMID: 28836033

2

Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy.

Carducci C, Leuzzi V, Scuderi M, De Negri AM, Gabrieli CB, Antonozzi I, Pontecorvi A. Carducci C, et al. Among authors: leuzzi v. Hum Genet. 1991 Oct;87(6):725-7. doi: 10.1007/BF00201733. Hum Genet. 1991. PMID: 1937476

3

Biochemical, clinical and neuroradiological (MRI) correlations in late-detected PKU patients.

Leuzzi V, Trasimeni G, Gualdi GF, Antonozzi I. Leuzzi V, et al. J Inherit Metab Dis. 1995;18(5):624-34. doi: 10.1007/BF02436009. J Inherit Metab Dis. 1995. PMID: 8598645

4

Screening of mtDNA mutations in Italian LHON pedigrees.

Carducci C, De Negri AM, Leuzzi V, Terregino C, Torella M, Pivetti Pezzi P, Antonozzi I. Carducci C, et al. Among authors: leuzzi v. J Inherit Metab Dis. 1996;19(2):127-9. doi: 10.1007/BF01799410. J Inherit Metab Dis. 1996. PMID: 8739946 No abstract available.

5

Automated method for the measurement of amino acids in urine by high-performance liquid chromatography.

Carducci C, Birarelli M, Leuzzi V, Santagata G, Serafini P, Antonozzi I. Carducci C, et al. Among authors: leuzzi v. J Chromatogr A. 1996 Apr 5;729(1-2):173-80. doi: 10.1016/0021-9673(95)00964-7. J Chromatogr A. 1996. PMID: 9004938

6

Neuropsychological and neuroradiological (MRI) variations during phenylalanine load: protective effect of valine, leucine, and isoleucine supplementation.

Leuzzi V, Fois D, Carducci C, Antonozzi I, Trasimeni G. Leuzzi V, et al. J Child Neurol. 1997 Aug;12(5):338-40. doi: 10.1177/088307389701200511. J Child Neurol. 1997. PMID: 9378904 No abstract available.

7

Subclinical visual impairment in phenylketonuria. A neurophysiological study (VEP-P) with clinical, biochemical, and neuroradiological (MRI) correlations.

Leuzzi V, Rinalduzzi S, Chiarotti F, Garzia P, Trasimeni G, Accornero N. Leuzzi V, et al. J Inherit Metab Dis. 1998 Jun;21(4):351-64. doi: 10.1023/a:1005346422918. J Inherit Metab Dis. 1998. PMID: 9700592

8

Derangement of the dopaminergic system in phenylketonuria: study of the event-related potential (P300).

Leuzzi V, Seri S, Cerquiglini A, Carducci C, Carducci C, Antonozzi I. Leuzzi V, et al. J Inherit Metab Dis. 2000 Jun;23(4):317-20. doi: 10.1023/a:1005646206348. J Inherit Metab Dis. 2000. PMID: 10896283 No abstract available.

9

Clinical significance of brain phenylalanine concentration assessed by in vivo proton magnetic resonance spectroscopy in phenylketonuria.

Leuzzi V, Bianchi MC, Tosetti M, Carducci CL, Carducci CA, Antonozzi I. Leuzzi V, et al. J Inherit Metab Dis. 2000 Sep;23(6):563-70. doi: 10.1023/a:1005621727560. J Inherit Metab Dis. 2000. PMID: 11032331

10

Two new severe mutations causing guanidinoacetate methyltransferase deficiency.

Carducci C, Leuzzi V, Carducci C, Prudente S, Mercuri L, Antonozzi I. Carducci C, et al. Among authors: leuzzi v. Mol Genet Metab. 2000 Dec;71(4):633-8. doi: 10.1006/mgme.2000.3108. Mol Genet Metab. 2000. PMID: 11136556

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