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

Year Number of Results
1962 1
1963 1
1964 2
1965 2
1967 1
1968 1
1969 4
1970 2
1971 2
1991 1
1994 1
1995 3
1997 1
1998 2
1999 2
2000 1
2001 5
2002 2
2003 1
2004 5
2006 3
2007 3
2008 3
2009 2
2010 7
2011 2
2012 3
2013 5
2014 2
2015 2
2016 4
2017 1
2019 3
2020 9
2021 16
2022 17
2023 11
2024 8

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128 results

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Page 1
Therapeutic Options in Hereditary Optic Neuropathies.
Amore G, Romagnoli M, Carbonelli M, Barboni P, Carelli V, La Morgia C. Amore G, et al. Drugs. 2021 Jan;81(1):57-86. doi: 10.1007/s40265-020-01428-3. Drugs. 2021. PMID: 33159657 Free PMC article. Review.
Artificial Intelligence to Detect Papilledema from Ocular Fundus Photographs.
Milea D, Najjar RP, Zhubo J, Ting D, Vasseneix C, Xu X, Aghsaei Fard M, Fonseca P, Vanikieti K, Lagrèze WA, La Morgia C, Cheung CY, Hamann S, Chiquet C, Sanda N, Yang H, Mejico LJ, Rougier M-B, Kho R, Thi Ha Chau T, Singhal S, Gohier P, Clermont-Vignal C, Cheng C-Y, Jonas JB, Yu-Wai-Man P, Fraser CL, Chen JJ, Ambika S, Miller NR, Liu Y, Newman NJ, Wong TY, Biousse V; BONSAI Group. Milea D, et al. N Engl J Med. 2020 Apr 30;382(18):1687-1695. doi: 10.1056/NEJMoa1917130. Epub 2020 Apr 14. N Engl J Med. 2020. PMID: 32286748
Treatment of multiple sclerosis in children: A brief overview.
Nicotera AG, Spoto G, Saia MC, Midiri M, Turriziani L, Amore G, Di Rosa G. Nicotera AG, et al. Among authors: amore g. Clin Immunol. 2022 Apr;237:108947. doi: 10.1016/j.clim.2022.108947. Epub 2022 Feb 2. Clin Immunol. 2022. PMID: 35123059 Review.
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease.
Calì E, Lin SJ, Rocca C, Sahin Y, Al Shamsi A, El Chehadeh S, Chaabouni M, Mankad K, Galanaki E, Efthymiou S, Sudhakar S, Athanasiou-Fragkouli A, Çelik T, Narlı N, Bianca S, Murphy D, De Carvalho Moreira FM; SYNaPS Study Group; Andrea Accogli, Petree C, Huang K, Monastiri K, Edizadeh M, Nardello R, Ognibene M, De Marco P, Ruggieri M, Zara F, Striano P, Şahin Y, Al-Gazali L, Abi Warde MT, Gerard B, Zifarelli G, Beetz C, Fortuna S, Soler M, Valente EM, Varshney G, Maroofian R, Salpietro V, Houlden H. Calì E, et al. Genet Med. 2022 Oct;24(10):2194-2203. doi: 10.1016/j.gim.2022.07.013. Epub 2022 Aug 24. Genet Med. 2022. PMID: 36001086 Free PMC article.
[Renal Replacement Therapy in Cancer Patients with AKI].
Pozzato M, Fenoglio R, Caruso N, Ceruti C, Amore G, Sciascia S, Roccatello D. Pozzato M, et al. Among authors: amore g. G Ital Nefrol. 2023 Oct 3;40(Suppl 81):2023-S81. G Ital Nefrol. 2023. PMID: 38007827 Review. Italian.
The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10.
Fiorini C, Ormanbekova D, Palombo F, Carbonelli M, Amore G, Romagnoli M, d'Agati P, Valentino ML, Barboni P, Cascavilla ML, De Negri A, Sadun F, Carta A, Testa F, Petruzzella V, Guerriero S, Bianchi Marzoli S, Carelli V, La Morgia C, Caporali L. Fiorini C, et al. Among authors: amore g. Brain. 2023 Sep 1;146(9):e67-e70. doi: 10.1093/brain/awad080. Brain. 2023. PMID: 36913248 Free PMC article. No abstract available.
128 results