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Seizure semiology of lesional frontal lobe epilepsies in children.
Battaglia D, Lettori D, Contaldo I, Veredice C, Sacco A, Vasco J, Martinelli D, Chieffo D, Tartaglione T, Colosimo C, Di Rocco C, Guzzetta F. Battaglia D, et al. Among authors: veredice c. Neuropediatrics. 2007 Dec;38(6):287-91. doi: 10.1055/s-2008-1062705. Neuropediatrics. 2007. PMID: 18461504
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
A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset.
De Rose DU, Gallini F, Battaglia DI, Tiberi E, Gaudino S, Contaldo I, Veredice C, Romeo DM, Massimi L, Asaro A, Cereda C, Vento G, Mercuri EM. De Rose DU, et al. Among authors: veredice c. Neurol Sci. 2021 Nov;42(11):4759-4765. doi: 10.1007/s10072-021-05480-z. Epub 2021 Jul 22. Neurol Sci. 2021. PMID: 34292449 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.
31 results