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

Year Number of Results
2008 1
2009 1
2010 4
2011 4
2012 2
2013 4
2014 5
2015 2
2016 1
2017 1
2018 4
2019 2
2020 2
2021 5
2022 5
2023 3
2024 2

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38 results

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Page 1
Brain abscess in pediatric age: a review.
Mameli C, Genoni T, Madia C, Doneda C, Penagini F, Zuccotti G. Mameli C, et al. Among authors: doneda c. Childs Nerv Syst. 2019 Jul;35(7):1117-1128. doi: 10.1007/s00381-019-04182-4. Epub 2019 May 6. Childs Nerv Syst. 2019. PMID: 31062139 Review.
Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder.
Accogli A, Lin SJ, Severino M, Kim SH, Huang K, Rocca C, Landsverk M, Zaki MS, Al-Maawali A, Srinivasan VM, Al-Thihli K, Schaefer GB, Davis M, Tonduti D, Doneda C, Marten LM, Mühlhausen C, Gomez M, Lamantea E, Mena R, Nizon M, Procaccio V, Begtrup A, Telegrafi A, Cui H, Schulz HL, Mohr J, Biskup S, Loos MA, Aráoz HV, Salpietro V, Keppen LD, Chitre M, Petree C, Raymond L, Vogt J, Sawyer LB, Basinger AA, Pedersen SV, Pearson TS, Grange DK, Lingappa L, McDunnah P, Horvath R, Cognè B, Isidor B, Hahn A, Gripp KW, Jafarnejad SM, Østergaard E, Prada CE, Ghezzi D, Gowda VK, Taylor RW, Sonenberg N, Houlden H, Sissler M, Varshney GK, Maroofian R. Accogli A, et al. Among authors: doneda c. Genet Med. 2023 Nov;25(11):100938. doi: 10.1016/j.gim.2023.100938. Epub 2023 Jul 13. Genet Med. 2023. PMID: 37454282 Free article.
Cerebellar dysplasia related to PIK3CA mutation: a three-case series.
Di Stasi M, Izzo G, Cattaneo E, Baraldini V, Doneda C, Righini A, Graziani D, Toto V, Parazzini C. Di Stasi M, et al. Among authors: doneda c. Neurogenetics. 2021 Mar;22(1):27-32. doi: 10.1007/s10048-020-00628-z. Epub 2020 Sep 8. Neurogenetics. 2021. PMID: 32901329
Neuroimaging of pediatric brain infections.
Triulzi F, Doneda C, Parazzini C. Triulzi F, et al. Among authors: doneda c. Expert Rev Anti Infect Ther. 2011 Jun;9(6):737-51. doi: 10.1586/eri.11.38. Expert Rev Anti Infect Ther. 2011. PMID: 21692676
Phenotypic spectrum of short-chain enoyl-Coa hydratase-1 (ECHS1) deficiency.
Masnada S, Parazzini C, Bini P, Barbarini M, Alberti L, Valente M, Chiapparini L, De Silvestri A, Doneda C, Iascone M, Saielli LA, Cereda C, Veggiotti P, Corbetta C, Tonduti D. Masnada S, et al. Among authors: doneda c. Eur J Paediatr Neurol. 2020 Sep;28:151-158. doi: 10.1016/j.ejpn.2020.07.007. Epub 2020 Jul 29. Eur J Paediatr Neurol. 2020. PMID: 32800686
38 results