Petrillo S - Search Results

1

Frataxin deficiency leads to reduced expression and impaired translocation of NF-E2-related factor (Nrf2) in cultured motor neurons.

D'Oria V, Petrini S, Travaglini L, Priori C, Piermarini E, Petrillo S, Carletti B, Bertini E, Piemonte F. D'Oria V, et al. Among authors: petrillo s. Int J Mol Sci. 2013 Apr 10;14(4):7853-65. doi: 10.3390/ijms14047853. Int J Mol Sci. 2013. PMID: 23574943 Free PMC article.

2

Pediatric reference intervals for muscle coenzyme Q(10).

Pastore A, Di Giovamberardino G, Petrillo S, Boenzi S, Bertini E, Dionisi-Vici C, Piemonte F. Pastore A, et al. Among authors: petrillo s. Biomarkers. 2012 Dec;17(8):764-6. doi: 10.3109/1354750X.2012.727029. Epub 2012 Oct 1. Biomarkers. 2012. PMID: 23020092

3

Glutathione metabolism in cobalamin deficiency type C (cblC).

Pastore A, Martinelli D, Piemonte F, Tozzi G, Boenzi S, Di Giovamberardino G, Petrillo S, Bertini E, Dionisi-Vici C. Pastore A, et al. Among authors: petrillo s. J Inherit Metab Dis. 2014 Jan;37(1):125-9. doi: 10.1007/s10545-013-9605-3. Epub 2013 Apr 9. J Inherit Metab Dis. 2014. PMID: 23568438

4

Glutathione: a redox signature in monitoring EPI-743 therapy in children with mitochondrial encephalomyopathies.

Pastore A, Petrillo S, Tozzi G, Carrozzo R, Martinelli D, Dionisi-Vici C, Di Giovamberardino G, Ceravolo F, Klein MB, Miller G, Enns GM, Bertini E, Piemonte F. Pastore A, et al. Among authors: petrillo s. Mol Genet Metab. 2013 Jun;109(2):208-14. doi: 10.1016/j.ymgme.2013.03.011. Epub 2013 Mar 24. Mol Genet Metab. 2013. PMID: 23583222

5

Glutathione imbalance in patients with X-linked adrenoleukodystrophy.

Petrillo S, Piemonte F, Pastore A, Tozzi G, Aiello C, Pujol A, Cappa M, Bertini E. Petrillo S, et al. Mol Genet Metab. 2013 Aug;109(4):366-70. doi: 10.1016/j.ymgme.2013.05.009. Epub 2013 May 22. Mol Genet Metab. 2013. PMID: 23768953 Free PMC article.

6

Frataxin silencing inactivates mitochondrial Complex I in NSC34 motoneuronal cells and alters glutathione homeostasis.

Carletti B, Piermarini E, Tozzi G, Travaglini L, Torraco A, Pastore A, Sparaco M, Petrillo S, Carrozzo R, Bertini E, Piemonte F. Carletti B, et al. Among authors: petrillo s. Int J Mol Sci. 2014 Apr 4;15(4):5789-806. doi: 10.3390/ijms15045789. Int J Mol Sci. 2014. PMID: 24714088 Free PMC article.

7

Additive effect of nuclear and mitochondrial mutations in a patient with mitochondrial encephalomyopathy.

Nesti C, Meschini MC, Meunier B, Sacchini M, Doccini S, Romano A, Petrillo S, Pezzini I, Seddiki N, Rubegni A, Piemonte F, Donati MA, Brasseur G, Santorelli FM. Nesti C, et al. Among authors: petrillo s. Hum Mol Genet. 2015 Jun 1;24(11):3248-56. doi: 10.1093/hmg/ddv078. Epub 2015 Mar 3. Hum Mol Genet. 2015. PMID: 25736212

8

Systemic Redox Biomarkers in Neurodegenerative Diseases.

Pastore A, Petrillo S, Piermarini E, Piemonte F. Pastore A, et al. Among authors: petrillo s. Curr Drug Metab. 2015;16(1):46-70. doi: 10.2174/138920021601150702161250. Curr Drug Metab. 2015. PMID: 26152129 Review.

9

DJ-1 modulates mitochondrial response to oxidative stress: clues from a novel diagnosis of PARK7.

Di Nottia M, Masciullo M, Verrigni D, Petrillo S, Modoni A, Rizzo V, Di Giuda D, Rizza T, Niceta M, Torraco A, Bianchi M, Santoro M, Bentivoglio AR, Bertini E, Piemonte F, Carrozzo R, Silvestri G. Di Nottia M, et al. Among authors: petrillo s. Clin Genet. 2017 Jul;92(1):18-25. doi: 10.1111/cge.12841. Epub 2016 Oct 6. Clin Genet. 2017. PMID: 27460976

10

Oxidative stress in Duchenne muscular dystrophy: focus on the NRF2 redox pathway.

Petrillo S, Pelosi L, Piemonte F, Travaglini L, Forcina L, Catteruccia M, Petrini S, Verardo M, D'Amico A, Musarò A, Bertini E. Petrillo S, et al. Hum Mol Genet. 2017 Jul 15;26(14):2781-2790. doi: 10.1093/hmg/ddx173. Hum Mol Genet. 2017. PMID: 28472288

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