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

Year Number of Results
1999 1
2000 1
2002 1
2003 1
2004 2
2005 1
2006 4
2007 1
2010 1
2011 1
2012 1
2013 6
2014 4
2015 8
2016 5
2017 3
2018 8
2019 8
2020 14
2021 12
2022 13
2023 0
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86 results
Results by year
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Page 1
Interhemispheric Pediatric Meningioma, YAP1 Fusion-Positive.
Esposito S, Marucci G, Antonelli M, Miele E, Modena P, Giagnacovo M, Massimino M, Biassoni V, Taddei M, Schiariti MP, Doniselli FM, Moscatelli M, Chiapparini L, Pollo B. Esposito S, et al. Among authors: moscatelli m. Diagnostics (Basel). 2022 Sep 29;12(10):2367. doi: 10.3390/diagnostics12102367. Diagnostics (Basel). 2022. PMID: 36292056 Free PMC article.
The Wafer Technique: Histomorphometric Results.
Merli M, Mariotti G, Mazzoni A, Moscatelli M, Pagliaro U, Nieri M. Merli M, et al. Among authors: moscatelli m. Int J Periodontics Restorative Dent. 2020 Nov/Dec;40(6):815-823. doi: 10.11607/prd.4280. Int J Periodontics Restorative Dent. 2020. PMID: 33151186
Selfing is the safest sex for Caenorhabditis tropicalis.
Noble LM, Yuen J, Stevens L, Moya N, Persaud R, Moscatelli M, Jackson JL, Zhang G, Chitrakar R, Baugh LR, Braendle C, Andersen EC, Seidel HS, Rockman MV. Noble LM, et al. Among authors: moscatelli m. Elife. 2021 Jan 11;10:e62587. doi: 10.7554/eLife.62587. Elife. 2021. PMID: 33427200 Free PMC article.
Abnormal cerebellar foliation in EBF3 mutation.
D'Arrigo S, Moscatelli M, Ciaccio C, Pantaleoni C, Castello R, Chiapparini L; TUDP Study Group. D'Arrigo S, et al. Among authors: moscatelli m. Neurology. 2020 May 26;94(21):933-935. doi: 10.1212/WNL.0000000000009486. Epub 2020 May 4. Neurology. 2020. PMID: 32366537 No abstract available.
3-Methylglutaconic Aciduria Type I: A Rare Cause of Late-Onset Leukoencephalopathy.
Benzoni C, Magri S, Moscatelli M, Fenu S, Caccia C, Taroni F, Salsano E, Di Bella D. Benzoni C, et al. Among authors: moscatelli m. Neurol Genet. 2022 Sep 7;8(5):e200023. doi: 10.1212/NXG.0000000000200023. eCollection 2022 Oct. Neurol Genet. 2022. PMID: 36092981 Free PMC article. No abstract available.
Hypomyelinating leukodystrophies in adults: Clinical and genetic features.
Di Bella D, Magri S, Benzoni C, Farina L, Maccagnano C, Sarto E, Moscatelli M, Baratta S, Ciano C, Piacentini SHMJ, Draghi L, Mauro E, Pareyson D, Gellera C, Taroni F, Salsano E. Di Bella D, et al. Among authors: moscatelli m. Eur J Neurol. 2021 Mar;28(3):934-944. doi: 10.1111/ene.14646. Epub 2020 Dec 3. Eur J Neurol. 2021. PMID: 33190326
86 results