Leuzzi V - Search Results

1

The expanding spectrum of movement disorders in genetic epilepsies.

Papandreou A, Danti FR, Spaull R, Leuzzi V, Mctague A, Kurian MA. Papandreou A, et al. Among authors: leuzzi v. Dev Med Child Neurol. 2020 Feb;62(2):178-191. doi: 10.1111/dmcn.14407. Epub 2019 Nov 29. Dev Med Child Neurol. 2020. PMID: 31784983 Free article. Review.

2

Brain creatine depletion: guanidinoacetate methyltransferase deficiency (improving with creatine supplementation).

Leuzzi V, Bianchi MC, Tosetti M, Carducci C, Cerquiglini CA, Cioni G, Antonozzi I. Leuzzi V, et al. Neurology. 2000 Nov 14;55(9):1407-9. doi: 10.1212/wnl.55.9.1407. Neurology. 2000. PMID: 11087795

3

Inborn errors of creatine metabolism and epilepsy: clinical features, diagnosis, and treatment.

Leuzzi V. Leuzzi V. J Child Neurol. 2002 Dec;17 Suppl 3:3S89-97; discussion 3S97. J Child Neurol. 2002. PMID: 12597058 Review.

4

Early-onset encephalopathy and cortical myoclonus in a boy with MECP2 gene mutation.

Leuzzi V, Di Sabato ML, Zollino M, Montanaro ML, Seri S. Leuzzi V, et al. Neurology. 2004 Nov 23;63(10):1968-70. doi: 10.1212/01.wnl.0000144350.97844.94. Neurology. 2004. PMID: 15557528

5

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.

6

Scale for evaluation of movement disorders in the first three years of life.

Battini R, Guzzetta A, Sgandurra G, Di Pietro R, Petacchi E, Mercuri E, Giannini MT, Leuzzi V, Cioni G. Battini R, et al. Among authors: leuzzi v. Pediatr Neurol. 2009 Apr;40(4):258-64. doi: 10.1016/j.pediatrneurol.2008.11.003. Pediatr Neurol. 2009. PMID: 19302937

7

A diagnostic algorithm for the evaluation of early onset genetic-metabolic epileptic encephalopathies.

Mastrangelo M, Celato A, Leuzzi V. Mastrangelo M, et al. Among authors: leuzzi v. Eur J Paediatr Neurol. 2012 Mar;16(2):179-91. doi: 10.1016/j.ejpn.2011.07.015. Epub 2011 Sep 21. Eur J Paediatr Neurol. 2012. PMID: 21940184 Review.

8

A new tyrosine hydroxylase genotype associated with early-onset severe encephalopathy.

Giovanniello T, Claps D, Carducci C, Carducci C, Blau N, Vigevano F, Antonozzi I, Leuzzi V. Giovanniello T, et al. Among authors: leuzzi v. J Child Neurol. 2012 Apr;27(4):523-5. doi: 10.1177/0883073811420717. Epub 2011 Sep 22. J Child Neurol. 2012. PMID: 21940685

9

Genes of early-onset epileptic encephalopathies: from genotype to phenotype.

Mastrangelo M, Leuzzi V. Mastrangelo M, et al. Among authors: leuzzi v. Pediatr Neurol. 2012 Jan;46(1):24-31. doi: 10.1016/j.pediatrneurol.2011.11.003. Pediatr Neurol. 2012. PMID: 22196487 Review.

10

Very early pattern of movement disorders in sepiapterin reductase deficiency.

Leuzzi V, Carducci C, Tolve M, Giannini MT, Angeloni A, Carducci C. Leuzzi V, et al. Neurology. 2013 Dec 10;81(24):2141-2. doi: 10.1212/01.wnl.0000437299.51312.5f. Epub 2013 Nov 8. Neurology. 2013. PMID: 24212389 No abstract available.

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