Chiarotti F - Search Results

1

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: chiarotti 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

2

Subclinical visual impairment in phenylketonuria. A neurophysiological study (VEP-P) with clinical, biochemical, and neuroradiological (MRI) correlations.

Leuzzi V, Rinalduzzi S, Chiarotti F, Garzia P, Trasimeni G, Accornero N. Leuzzi V, et al. Among authors: chiarotti f. J Inherit Metab Dis. 1998 Jun;21(4):351-64. doi: 10.1023/a:1005346422918. J Inherit Metab Dis. 1998. PMID: 9700592

3

Executive function impairment in early-treated PKU subjects with normal mental development.

Leuzzi V, Pansini M, Sechi E, Chiarotti F, Carducci C, Levi G, Antonozzi I. Leuzzi V, et al. Among authors: chiarotti f. J Inherit Metab Dis. 2004;27(2):115-25. doi: 10.1023/B:BOLI.0000028781.94251.1f. J Inherit Metab Dis. 2004. PMID: 15159642

4

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. Among authors: chiarotti f. J Inherit Metab Dis. 2006 Feb;29(1):38-46. doi: 10.1007/s10545-006-0096-3. J Inherit Metab Dis. 2006. PMID: 16601866

5

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. Among authors: chiarotti f. 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

6

Urinary neopterin and phenylalanine loading test as tools for the biochemical diagnosis of segawa disease.

Leuzzi V, Carducci C, Chiarotti F, D'Agnano D, Giannini MT, Antonozzi I, Carducci C. Leuzzi V, et al. Among authors: chiarotti f. JIMD Rep. 2013;7:67-75. doi: 10.1007/8904_2012_144. Epub 2012 Apr 18. JIMD Rep. 2013. PMID: 23430498 Free PMC article.

7

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: chiarotti 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

8

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: chiarotti 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

9

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: chiarotti 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

10

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. Among authors: chiarotti f. 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

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