Leuzzi V - Search Results

1

KCNQ2 encephalopathy manifesting with Rett-like features: A follow-up into adulthood.

Mastrangelo M, Manti F, Giannini MT, Guerrini R, Leuzzi V. Mastrangelo M, et al. Among authors: leuzzi v. Neurol Genet. 2020 Sep 8;6(5):e510. doi: 10.1212/NXG.0000000000000510. eCollection 2020 Oct. Neurol Genet. 2020. PMID: 33134511 Free PMC article. No abstract available.

2

Movement disorder-childhood rating scale: reliability and validity.

Battini R, Sgandurra G, Petacchi E, Guzzetta A, Di Pietro R, Giannini MT, Leuzzi V, Mercuri E, Cioni G. Battini R, et al. Among authors: leuzzi v. Pediatr Neurol. 2008 Oct;39(4):259-65. doi: 10.1016/j.pediatrneurol.2008.07.002. Pediatr Neurol. 2008. PMID: 18805364 Clinical Trial.

3

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

4

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.

5

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.

6

Marangi G, Leuzzi V, Manti F, Lattante S, Orteschi D, Pecile V, Neri G, Zollino M. Marangi G, et al. Among authors: leuzzi v. Eur J Hum Genet. 2013 Feb;21(2):229-32. doi: 10.1038/ejhg.2012.79. Epub 2012 May 2. Eur J Hum Genet. 2013. PMID: 22549410 Free PMC article.

7

Mitochondrial neurogastrointestinal encephalomyopathy: novel pathogenic mutations in thymidine phosphorylase gene in two Italian brothers.

Libernini L, Lupis C, Mastrangelo M, Carrozzo R, Santorelli FM, Inghilleri M, Leuzzi V. Libernini L, et al. Among authors: leuzzi v. Neuropediatrics. 2012 Aug;43(4):201-8. doi: 10.1055/s-0032-1315431. Epub 2012 May 22. Neuropediatrics. 2012. PMID: 22618301

8

Inborn errors of creatine metabolism and epilepsy.

Leuzzi V, Mastrangelo M, Battini R, Cioni G. Leuzzi V, et al. Epilepsia. 2013 Feb;54(2):217-27. doi: 10.1111/epi.12020. Epub 2012 Nov 13. Epilepsia. 2013. PMID: 23157605 Free article. Review.

9

A new case of malonic aciduria with a presymptomatic diagnosis and an early treatment.

Celato A, Mitola C, Tolve M, Giannini MT, De Leo S, Carducci C, Carducci C, Leuzzi V. Celato A, et al. Among authors: leuzzi v. Brain Dev. 2013 Aug;35(7):675-80. doi: 10.1016/j.braindev.2012.10.014. Epub 2012 Nov 22. Brain Dev. 2013. PMID: 23177061

10

Transdermal rotigotine in the treatment of aromatic L-amino acid decarboxylase deficiency.

Mastrangelo M, Caputi C, Galosi S, Giannini MT, Leuzzi V. Mastrangelo M, et al. Among authors: leuzzi v. Mov Disord. 2013 Apr;28(4):556-7. doi: 10.1002/mds.25303. Epub 2013 Feb 6. Mov Disord. 2013. PMID: 23390030 No abstract available.

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