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

Year Number of Results
2003 1
2004 1
2006 1
2007 4
2008 3
2009 2
2010 2
2011 2
2012 1
2013 1
2014 1
2015 3
2016 1
2017 2
2018 1
2019 5
2020 5
2021 5
2022 3
2023 6
2024 1

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Page 1
Complete agenesis of corpus callosum and unilateral cortical formation anomalies detected on fetal MR imaging: a phenotype strongly associated with the male fetuses.
Vola EA, Griffiths PD, Parazzini C, Palumbo G, Scola E, Severino M, Pinelli L, D'Errico I, Di Maurizio M, Pecco N, Rossi A, Triulzi F, Righini A. Vola EA, et al. Among authors: palumbo g. Eur Radiol. 2023 Mar;33(3):2258-2265. doi: 10.1007/s00330-022-09173-9. Epub 2022 Oct 20. Eur Radiol. 2023. PMID: 36264312
Cerebral folate transporter deficiency syndrome in three siblings: Why genetic testing for developmental and epileptic encephalopathies should be performed early and include the FOLR1 gene.
Brunetti S, Malerba L, Giordano L, Parrini E, Guerrini R, Palumbo G, Parazzini C, Bestetti I, Accorsi P. Brunetti S, et al. Among authors: palumbo g. Am J Med Genet A. 2021 Aug;185(8):2526-2531. doi: 10.1002/ajmg.a.62345. Epub 2021 May 19. Am J Med Genet A. 2021. PMID: 34008900
Teaching NeuroImage: Nitromethane-Induced Acute Reversible Encephalopathy.
Palumbo G, Besana M, Ananiadou S, Giordano C, Maccabelli G, Riccio M, Campana C, Giossi A, Piovan E, Lonati D, Pinelli L. Palumbo G, et al. Neurology. 2021 Sep 28;97(13):e1361-e1362. doi: 10.1212/WNL.0000000000012178. Epub 2021 May 12. Neurology. 2021. PMID: 33980707 No abstract available.
43 results