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

Year Number of Results
2005 2
2006 1
2007 3
2008 1
2009 4
2010 2
2011 1
2012 1
2019 1
2020 2
2021 5
2022 6
2023 9
2024 2

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31 results

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Page 1
A systematic review on gender dysphoria in adolescents and young adults: focus on suicidal and self-harming ideation and behaviours.
Marconi E, Monti L, Marfoli A, Kotzalidis GD, Janiri D, Cianfriglia C, Moriconi F, Costa S, Veredice C, Sani G, Chieffo DPR. Marconi E, et al. Among authors: veredice c. Child Adolesc Psychiatry Ment Health. 2023 Sep 21;17(1):110. doi: 10.1186/s13034-023-00654-3. Child Adolesc Psychiatry Ment Health. 2023. PMID: 37735422 Free PMC article. Review.
Adult phenotype in Koolen-de Vries/KANSL1 haploinsufficiency syndrome.
Amenta S, Frangella S, Marangi G, Lattante S, Ricciardi S, Doronzio PN, Orteschi D, Veredice C, Contaldo I, Zampino G, Gentile M, Scarano E, Graziano C, Zollino M. Amenta S, et al. Among authors: veredice c. J Med Genet. 2022 Feb;59(2):189-195. doi: 10.1136/jmedgenet-2020-107225. Epub 2020 Dec 24. J Med Genet. 2022. PMID: 33361104
Cortical Visual Impairment in CDKL5 Deficiency Disorder.
Quintiliani M, Ricci D, Petrianni M, Leone S, Orazi L, Amore F, Gambardella ML, Contaldo I, Veredice C, Perulli M, Musto E, Mercuri EM, Battaglia DI. Quintiliani M, et al. Among authors: veredice c. Front Neurol. 2022 Jan 26;12:805745. doi: 10.3389/fneur.2021.805745. eCollection 2021. Front Neurol. 2022. PMID: 35153983 Free PMC article.
Visual Function in Children with GNAO1-Related Encephalopathy.
Gambardella ML, Pede E, Orazi L, Leone S, Quintiliani M, Amorelli GM, Petrianni M, Galanti M, Amore F, Musto E, Perulli M, Contaldo I, Veredice C, Mercuri EM, Battaglia DI, Ricci D. Gambardella ML, et al. Among authors: veredice c. Genes (Basel). 2023 Feb 22;14(3):544. doi: 10.3390/genes14030544. Genes (Basel). 2023. PMID: 36980817 Free PMC article.
Epilepsy and BRAF Mutations: Phenotypes, Natural History and Genotype-Phenotype Correlations.
Battaglia DI, Gambardella ML, Veltri S, Contaldo I, Chillemi G, Veredice C, Quintiliani M, Leoni C, Onesimo R, Verdolotti T, Radio FC, Martinelli D, Trivisano M, Specchio N, Dravet C, Tartaglia M, Zampino G. Battaglia DI, et al. Among authors: veredice c. Genes (Basel). 2021 Aug 26;12(9):1316. doi: 10.3390/genes12091316. Genes (Basel). 2021. PMID: 34573299 Free PMC article.
Chiari 1 Malformation and Epilepsy in Children: A Missing Relationship.
Massimi L, Palombi D, Contaldo I, Veredice C, Chieffo DRP, Calandrelli R, Tamburrini G, Battaglia DI. Massimi L, et al. Among authors: veredice c. J Clin Med. 2022 Oct 20;11(20):6182. doi: 10.3390/jcm11206182. J Clin Med. 2022. PMID: 36294502 Free PMC article.
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders.
Nicita F, Ginevrino M, Travaglini L, D'Arrigo S, Zorzi G, Borgatti R, Terrone G, Catteruccia M, Vasco G, Brankovic V, Siliquini S, Romano S, Veredice C, Pedemonte M, Armando M, Lettori D, Stregapede F, Bosco L, Sferra A, Tessarollo V, Romaniello R, Ristori G, Bertini E, Valente EM, Zanni G. Nicita F, et al. Among authors: veredice c. J Med Genet. 2021 Jul;58(7):475-483. doi: 10.1136/jmedgenet-2020-107007. Epub 2020 Jul 31. J Med Genet. 2021. PMID: 32737135
Fighting autoinflammation in FIRES: The role of interleukins and early immunomodulation.
Perulli M, Cicala G, Turrini I, Musto E, Quintiliani M, Gambardella ML, Pulitanò SM, Bompard S, Staccioli S, Carmillo L, Di Sante G, Ria F, Veredice C, Contaldo I, Battaglia D. Perulli M, et al. Among authors: veredice c. Epilepsy Behav Rep. 2022 Feb 22;18:100531. doi: 10.1016/j.ebr.2022.100531. eCollection 2022. Epilepsy Behav Rep. 2022. PMID: 35356746 Free PMC article.
31 results