Nardecchia F - Search Results

1

Improvement of Movement Disorder and Neurodevelopment under Selegiline in a CLTC-Deficient Patient.

Nardecchia F, Bove R, Pollini L, Giannini MT, Manti F, De Giorgi A, Papoff P, Martinelli S, Leuzzi V. Nardecchia F, et al. Mov Disord Clin Pract. 2023 Jul 19;10(9):1430-1432. doi: 10.1002/mdc3.13834. eCollection 2023 Sep. Mov Disord Clin Pract. 2023. PMID: 37772301 Free PMC article. No abstract available.

2

Metabolic epilepsy: an update.

Papetti L, Parisi P, Leuzzi V, Nardecchia F, Nicita F, Ursitti F, Marra F, Paolino MC, Spalice A. Papetti L, et al. Among authors: nardecchia f. Brain Dev. 2013 Oct;35(9):827-41. doi: 10.1016/j.braindev.2012.11.010. Epub 2012 Dec 27. Brain Dev. 2013. PMID: 23273990 Review.

3

Neurocognitive and neuroimaging outcome of early treated young adult PKU patients: A longitudinal study.

Nardecchia F, Manti F, Chiarotti F, Carducci C, Carducci C, Leuzzi V. Nardecchia F, et al. Mol Genet Metab. 2015 Jun-Jul;115(2-3):84-90. doi: 10.1016/j.ymgme.2015.04.003. Epub 2015 Apr 29. Mol Genet Metab. 2015. PMID: 25952249

4

The outcome of white matter abnormalities in early treated phenylketonuric patients: A retrospective longitudinal long-term study.

Mastrangelo M, Chiarotti F, Berillo L, Caputi C, Carducci C, Di Biasi C, Manti F, Nardecchia F, Leuzzi V. Mastrangelo M, et al. Among authors: nardecchia f. Mol Genet Metab. 2015 Nov;116(3):171-7. doi: 10.1016/j.ymgme.2015.08.005. Epub 2015 Aug 10. Mol Genet Metab. 2015. PMID: 26283467

5

Psychiatric disorders in adolescent and young adult patients with phenylketonuria.

Manti F, Nardecchia F, Chiarotti F, Carducci C, Carducci C, Leuzzi V. Manti F, et al. Among authors: nardecchia f. Mol Genet Metab. 2016 Jan;117(1):12-8. doi: 10.1016/j.ymgme.2015.11.006. Epub 2015 Nov 14. Mol Genet Metab. 2016. PMID: 26655635

6

Erythrocyte-mediated delivery of recombinant enzymes.

Leuzzi V, Rossi L, Gabucci C, Nardecchia F, Magnani M. Leuzzi V, et al. Among authors: nardecchia f. J Inherit Metab Dis. 2016 Jul;39(4):519-30. doi: 10.1007/s10545-016-9926-0. Epub 2016 Mar 30. J Inherit Metab Dis. 2016. PMID: 27026098 Review.

7

Altered tetrahydrobiopterin metabolism in patients with phenylalanine hydroxylase deficiency.

Nardecchia F, Chiarotti F, Carducci C, Santagata S, Valentini G, Angeloni A, Blau N, Leuzzi V. Nardecchia F, et al. Eur J Pediatr. 2017 Jul;176(7):917-924. doi: 10.1007/s00431-017-2932-x. Epub 2017 May 24. Eur J Pediatr. 2017. PMID: 28540433

8

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: nardecchia f. 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

9

Targeting mGlu5 Metabotropic Glutamate Receptors in the Treatment of Cognitive Dysfunction in a Mouse Model of Phenylketonuria.

Nardecchia F, Orlando R, Iacovelli L, Colamartino M, Fiori E, Leuzzi V, Piccinin S, Nistico R, Puglisi-Allegra S, Di Menna L, Battaglia G, Nicoletti F, Pascucci T. Nardecchia F, et al. Front Neurosci. 2018 Mar 16;12:154. doi: 10.3389/fnins.2018.00154. eCollection 2018. Front Neurosci. 2018. PMID: 29615849 Free PMC article.

10

Neurotransmitter trafficking defect in a patient with clathrin (CLTC) variation presenting with intellectual disability and early-onset parkinsonism.

Manti F, Nardecchia F, Barresi S, Venditti M, Pizzi S, Hamdan FF, Blau N, Burlina A, Tartaglia M, Leuzzi V. Manti F, et al. Among authors: nardecchia f. Parkinsonism Relat Disord. 2019 Apr;61:207-210. doi: 10.1016/j.parkreldis.2018.10.012. Epub 2018 Oct 11. Parkinsonism Relat Disord. 2019. PMID: 30337205

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