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

Year Number of Results
2002 2
2003 4
2004 2
2006 2
2007 1
2008 1
2009 1
2010 2
2011 4
2012 3
2013 4
2014 4
2015 4
2016 3
2017 4
2018 7
2019 2
2020 10
2021 10
2022 12
2023 9
2024 1

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89 results

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Page 1
Metabolic rewiring and autophagy inhibition correct lysosomal storage disease in mucopolysaccharidosis IIIB.
Scarcella M, Scerra G, Ciampa M, Caterino M, Costanzo M, Rinaldi L, Feliciello A, Anzilotti S, Fiorentino C, Renna M, Ruoppolo M, Pavone LM, D'Agostino M, De Pasquale V. Scarcella M, et al. Among authors: ruoppolo m. iScience. 2024 Jan 29;27(3):108959. doi: 10.1016/j.isci.2024.108959. eCollection 2024 Mar 15. iScience. 2024. PMID: 38361619 Free PMC article.
Human wild-type and D76N β2-microglobulin variants are significant proteotoxic and metabolic stressors for transgenic C. elegans.
Raimondi S, Faravelli G, Nocerino P, Mondani V, Baruffaldi A, Marchese L, Mimmi MC, Canetti D, Verona G, Caterino M, Ruoppolo M, Mangione PP, Bellotti V, Lavatelli F, Giorgetti S. Raimondi S, et al. Among authors: ruoppolo m. FASEB Bioadv. 2023 Oct 25;5(11):484-505. doi: 10.1096/fba.2023-00073. eCollection 2023 Nov. FASEB Bioadv. 2023. PMID: 37936921 Free PMC article.
Sex-Gender-Based Differences in Metabolic Diseases.
Campesi I, Ruoppolo M, Franconi F, Caterino M, Costanzo M. Campesi I, et al. Among authors: ruoppolo m. Handb Exp Pharmacol. 2023;282:241-257. doi: 10.1007/164_2023_683. Handb Exp Pharmacol. 2023. PMID: 37528324
Contribution of Genetic Test to Early Diagnosis of Methylenetetrahydrofolate Reductase (MTHFR) Deficiency: The Experience of a Reference Center in Southern Italy.
Barretta F, Uomo F, Fecarotta S, Albano L, Crisci D, Verde A, Fisco MG, Gallo G, Dottore Stagna D, Pricolo MR, Alagia M, Terrone G, Rossi A, Parenti G, Ruoppolo M, Mazzaccara C, Frisso G. Barretta F, et al. Among authors: ruoppolo m. Genes (Basel). 2023 Apr 26;14(5):980. doi: 10.3390/genes14050980. Genes (Basel). 2023. PMID: 37239340 Free PMC article.
Liver-directed gene therapy for ornithine aminotransferase deficiency.
Boffa I, Polishchuk E, De Stefano L, Dell'Aquila F, Nusco E, Marrocco E, Audano M, Pedretti S, Caterino M, Bellezza I, Ruoppolo M, Mitro N, Cellini B, Auricchio A, Brunetti-Pierri N. Boffa I, et al. Among authors: ruoppolo m. EMBO Mol Med. 2023 Apr 11;15(4):e17033. doi: 10.15252/emmm.202217033. Epub 2023 Jan 17. EMBO Mol Med. 2023. PMID: 36647689 Free PMC article.
Lipidomic alterations in human saliva from cystic fibrosis patients.
Caterino M, Fedele R, Carnovale V, Castaldo A, Gelzo M, Iacotucci P, Ruoppolo M, Castaldo G. Caterino M, et al. Among authors: ruoppolo m. Sci Rep. 2023 Jan 12;13(1):600. doi: 10.1038/s41598-022-24429-6. Sci Rep. 2023. PMID: 36635275 Free PMC article.
89 results