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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2014 2
2015 2
2016 4
2017 3
2018 2
2019 3
2020 10
2021 8
2022 5
2023 9
2024 1

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45 results

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Page 1
Converging Role for REEP1/SPG31 in Oxidative Stress.
Naef V, Meschini MC, Tessa A, Morani F, Corsinovi D, Ogi A, Marchese M, Ori M, Santorelli FM, Doccini S. Naef V, et al. Among authors: doccini s. Int J Mol Sci. 2023 Feb 9;24(4):3527. doi: 10.3390/ijms24043527. Int J Mol Sci. 2023. PMID: 36834939 Free PMC article.
Tackling Dysfunction of Mitochondrial Bioenergetics in the Brain.
Zanfardino P, Doccini S, Santorelli FM, Petruzzella V. Zanfardino P, et al. Among authors: doccini s. Int J Mol Sci. 2021 Aug 3;22(15):8325. doi: 10.3390/ijms22158325. Int J Mol Sci. 2021. PMID: 34361091 Free PMC article. Review.
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies.
Dosi C, Rubegni A, Baldacci J, Galatolo D, Doccini S, Astrea G, Berardinelli A, Bruno C, Bruno G, Comi GP, Donati MA, Dotti MT, Filosto M, Fiorillo C, Giannini F, Gigli GL, Grandis M, Lopergolo D, Magri F, Maioli MA, Malandrini A, Massa R, Matà S, Melani F, Messina S, Mignarri A, Moggio M, Pennisi EM, Pegoraro E, Ricci G, Sacchini M, Schenone A, Sampaolo S, Sciacco M, Siciliano G, Tasca G, Tonin P, Tupler R, Valente M, Volpi N, Cassandrini D, Santorelli FM. Dosi C, et al. Among authors: doccini s. Genes (Basel). 2023 Jan 23;14(2):298. doi: 10.3390/genes14020298. Genes (Basel). 2023. PMID: 36833224 Free PMC article.
Tanshinone IIA and Cryptotanshinone Counteract Inflammation by Regulating Gene and miRNA Expression in Human SGBS Adipocytes.
Carpi S, Quarta S, Doccini S, Saviano A, Marigliano N, Polini B, Massaro M, Carluccio MA, Calabriso N, Wabitsch M, Santorelli FM, Cecchini M, Maione F, Nieri P, Scoditti E. Carpi S, et al. Among authors: doccini s. Biomolecules. 2023 Jun 23;13(7):1029. doi: 10.3390/biom13071029. Biomolecules. 2023. PMID: 37509065 Free PMC article.
Bi-allelic variants in MDH2: Expanding the clinical phenotype.
Ticci C, Nesti C, Rubegni A, Doccini S, Baldacci J, Dal Canto F, Ragni L, Cordelli DM, Donati MA, Santorelli FM. Ticci C, et al. Among authors: doccini s. Clin Genet. 2022 Feb;101(2):260-264. doi: 10.1111/cge.14088. Epub 2021 Nov 22. Clin Genet. 2022. PMID: 34766628
Additive effect of DNAJC30 and NDUFA9 mutations causing Leigh syndrome.
Nesti C, Ticci C, Rubegni A, Doccini S, Scaturro G, Vetro A, Guerrini R, Santorelli FM, Procopio E. Nesti C, et al. Among authors: doccini s. J Neurol. 2023 Jun;270(6):3266-3269. doi: 10.1007/s00415-023-11673-7. Epub 2023 Mar 20. J Neurol. 2023. PMID: 36939934 No abstract available.
Expanding the clinical and genetic heterogeneity of SPAX5.
Dosi C, Galatolo D, Rubegni A, Doccini S, Pasquariello R, Nesti C, Sicca F, Barghigiani M, Battini R, Tessa A, Santorelli FM. Dosi C, et al. Among authors: doccini s. Ann Clin Transl Neurol. 2020 Apr;7(4):595-601. doi: 10.1002/acn3.51024. Epub 2020 Apr 1. Ann Clin Transl Neurol. 2020. PMID: 32237276 Free PMC article.
45 results