Leuzzi V - Search Results

1

A new form of cerebral folate deficiency with severe self-injurious behaviour.

Leuzzi V, Mastrangelo M, Celato A, Carducci C, Carducci C. Leuzzi V, et al. Acta Paediatr. 2012 Nov;101(11):e482-3. doi: 10.1111/j.1651-2227.2012.02800.x. Epub 2012 Sep 13. Acta Paediatr. 2012. PMID: 22861007 No abstract available.

2

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.

3

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

4

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

5

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.

Carducci C, Birarelli M, Santagata P, Leuzzi V, Carducci C, Antonozzi I. Carducci C, et al. Among authors: leuzzi v. J Chromatogr B Biomed Sci Appl. 2001 May 5;755(1-2):343-8. doi: 10.1016/s0378-4347(01)00052-4. J Chromatogr B Biomed Sci Appl. 2001. PMID: 11393723

6

Autosomal dominant GTP-CH deficiency presenting as a dopa-responsive myoclonus-dystonia syndrome.

Leuzzi V, Carducci C, Carducci C, Cardona F, Artiola C, Antonozzi I. Leuzzi V, et al. Neurology. 2002 Oct 22;59(8):1241-3. doi: 10.1212/wnl.59.8.1241. Neurology. 2002. PMID: 12391354

7

Quantitative determination of guanidinoacetate and creatine in dried blood spot by flow injection analysis-electrospray tandem mass spectrometry.

Carducci C, Santagata S, Leuzzi V, Carducci C, Artiola C, Giovanniello T, Battini R, Antonozzi I. Carducci C, et al. Among authors: leuzzi v. Clin Chim Acta. 2006 Feb;364(1-2):180-7. doi: 10.1016/j.cca.2005.06.016. Epub 2005 Sep 28. Clin Chim Acta. 2006. PMID: 16197934

8

The spectrum of phenylalanine variations under tetrahydrobiopterin load in subjects affected by phenylalanine hydroxylase deficiency.

Leuzzi V, Carducci C, Carducci C, Chiarotti F, Artiola C, Giovanniello T, Antonozzi I. Leuzzi V, et al. J Inherit Metab Dis. 2006 Feb;29(1):38-46. doi: 10.1007/s10545-006-0096-3. J Inherit Metab Dis. 2006. PMID: 16601866

9

The pathogenesis of the white matter abnormalities in phenylketonuria. A multimodal 3.0 tesla MRI and magnetic resonance spectroscopy (1H MRS) study.

Leuzzi V, Tosetti M, Montanaro D, Carducci C, Artiola C, Carducci C, Antonozzi I, Burroni M, Carnevale F, Chiarotti F, Popolizio T, Giannatempo GM, D'Alesio V, Scarabino T. Leuzzi V, et al. J Inherit Metab Dis. 2007 Apr;30(2):209-16. doi: 10.1007/s10545-006-0399-4. Epub 2007 Jan 23. J Inherit Metab Dis. 2007. PMID: 17245558

10

Vigabatrin improves paroxysmal dystonia in succinic semialdehyde dehydrogenase deficiency.

Leuzzi V, Di Sabato ML, Deodato F, Rizzo C, Boenzi S, Carducci C, Malaspina P, Liberanome C, Dionisi-Vici C. Leuzzi V, et al. Neurology. 2007 Apr 17;68(16):1320-1. doi: 10.1212/01.wnl.0000259537.54082.6d. Neurology. 2007. PMID: 17438226 Free article. No abstract available.

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