Manti F - Search Results

1

Age-related psychophysiological vulnerability to phenylalanine in phenylketonuria.

Leuzzi V, Mannarelli D, Manti F, Pauletti C, Locuratolo N, Carducci C, Carducci C, Vanacore N, Fattapposta F. Leuzzi V, et al. Among authors: manti f. Front Pediatr. 2014 Jun 23;2:57. doi: 10.3389/fped.2014.00057. eCollection 2014. Front Pediatr. 2014. PMID: 25003100 Free PMC article.

2

Marangi G, Leuzzi V, Manti F, Lattante S, Orteschi D, Pecile V, Neri G, Zollino M. Marangi G, et al. Among authors: manti f. 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.

3

Running apraxia as a presenting symptom of neuronal ceroid lipofuscinosis 6.

Leuzzi V, Garavaglia B, Manti F, Bertino S, Nardocci N. Leuzzi V, et al. Among authors: manti f. Mov Disord. 2014 Feb;29(2):277-8. doi: 10.1002/mds.25725. Epub 2013 Oct 22. Mov Disord. 2014. PMID: 24151230 No abstract available.

4

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. Among authors: manti f. 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

5

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: manti 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

6

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. 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

7

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. 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

8

Screening for Developmental Disorders in 3- and 4-Year-Old Italian Children: A Preliminary Study.

Catino E, Di Trani M, Giovannone F, Manti F, Nunziata L, Piccari F, Sirchia V, Vannucci L, Sogos C. Catino E, et al. Among authors: manti f. Front Pediatr. 2017 Aug 29;5:181. doi: 10.3389/fped.2017.00181. eCollection 2017. Front Pediatr. 2017. PMID: 28900613 Free PMC article.

9

Living with phenylketonuria in adulthood: The PKU ATTITUDE study.

Cazzorla C, Bensi G, Biasucci G, Leuzzi V, Manti F, Musumeci A, Papadia F, Stoppioni V, Tummolo A, Vendemiale M, Polo G, Burlina A. Cazzorla C, et al. Among authors: manti f. Mol Genet Metab Rep. 2018 Jul 11;16:39-45. doi: 10.1016/j.ymgmr.2018.06.007. eCollection 2018 Sep. Mol Genet Metab Rep. 2018. PMID: 30069431 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. 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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