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Year Number of Results
2020 1
2021 5
2022 4
2023 5
2024 2

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14 results

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Page 1
Redox Imbalance in Neurological Disorders in Adults and Children.
Rey F, Berardo C, Maghraby E, Mauri A, Messa L, Esposito L, Casili G, Ottolenghi S, Bonaventura E, Cuzzocrea S, Zuccotti G, Tonduti D, Esposito E, Paterniti I, Cereda C, Carelli S. Rey F, et al. Among authors: bonaventura e. Antioxidants (Basel). 2023 Apr 20;12(4):965. doi: 10.3390/antiox12040965. Antioxidants (Basel). 2023. PMID: 37107340 Free PMC article. Review.
Newborn screening for X-linked adrenoleukodystrophy in Italy: Diagnostic algorithm and disease monitoring.
Bonaventura E, Alberti L, Lucchi S, Cappelletti L, Fazzone S, Cattaneo E, Bellini M, Izzo G, Parazzini C, Bosetti A, Di Profio E, Fiore G, Ferrario M, Mameli C, Sangiorgio A, Masnada S, Zuccotti GV, Veggiotti P, Spaccini L, Iascone M, Verduci E, Cereda C, Tonduti D; XALD-NBS Study Group. Bonaventura E, et al. Front Neurol. 2023 Jan 9;13:1072256. doi: 10.3389/fneur.2022.1072256. eCollection 2022. Front Neurol. 2023. PMID: 36698902 Free PMC article.
Anomalous Optical Properties of KTN:Li Ferroelectric Supercrystals.
Falsi L, Macis S, Gelkop Y, Tartara L, Bonaventura E, Di Pietro P, Perucchi A, Garcia Y, Perepelitsa G, DelRe E, Agranat AJ, Lupi S. Falsi L, et al. Among authors: bonaventura e. Nanomaterials (Basel). 2023 Feb 27;13(5):899. doi: 10.3390/nano13050899. Nanomaterials (Basel). 2023. PMID: 36903777 Free PMC article.
Clinical, molecular and glycophenotype insights in SLC39A8-CDG.
Bonaventura E, Barone R, Sturiale L, Pasquariello R, Alessandrì MG, Pinto AM, Renieri A, Panteghini C, Garavaglia B, Cioni G, Battini R. Bonaventura E, et al. Orphanet J Rare Dis. 2021 Jul 10;16(1):307. doi: 10.1186/s13023-021-01941-y. Orphanet J Rare Dis. 2021. PMID: 34246313 Free PMC article.
Optical and thermal responses of silicene in Xene heterostructures.
Bonaventura E, Dhungana DS, Martella C, Grazianetti C, Macis S, Lupi S, Bonera E, Molle A. Bonaventura E, et al. Nanoscale Horiz. 2022 Jul 25;7(8):924-930. doi: 10.1039/d2nh00219a. Nanoscale Horiz. 2022. PMID: 35788614 Free PMC article.
Menkes disease complicated by concurrent ACY1 deficiency: A case report.
Mauri A, Saielli LA, Alfei E, Iascone M, Marchetti D, Cattaneo E, Di Lauro A, Antonelli L, Alberti L, Bonaventura E, Veggiotti P, Spaccini L, Cereda C. Mauri A, et al. Among authors: bonaventura e. Front Genet. 2023 Mar 2;14:1077625. doi: 10.3389/fgene.2023.1077625. eCollection 2023. Front Genet. 2023. PMID: 36936426 Free PMC article.
Corrigendum: Newborn screening for X-linked adrenoleukodystrophy in Italy: diagnostic algorithm and disease monitoring.
Bonaventura E, Alberti L, Lucchi S, Cappelletti L, Fazzone S, Cattaneo E, Bellini M, Izzo G, Parazzini C, Bosetti A, Di Profio E, Fiore G, Ferrario M, Mameli C, Sangiorgio A, Masnada S, Zuccotti GV, Veggiotti P, Spaccini L, Iascone M, Verduci E, Cereda C, Tonduti D; XALD-NBS Study Group. Bonaventura E, et al. Front Neurol. 2024 Mar 6;15:1376447. doi: 10.3389/fneur.2024.1376447. eCollection 2024. Front Neurol. 2024. PMID: 38510379 Free PMC article.
14 results