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CDKL5 deficiency disorder in males: Five new variants and review of the literature.
Siri B, Varesio C, Freri E, Darra F, Gana S, Mei D, Porta F, Fontana E, Galati G, Solazzi R, Niceta M, Veggiotti P, Alfei E. Siri B, et al. Among authors: fontana e. Eur J Paediatr Neurol. 2021 Jul;33:9-20. doi: 10.1016/j.ejpn.2021.04.007. Epub 2021 Apr 30. Eur J Paediatr Neurol. 2021. PMID: 33989939 Review.
Myoclonic status in nonprogressive encephalopathies.
Dalla Bernardina B, Fontana E, Darra F. Dalla Bernardina B, et al. Among authors: fontana e. Adv Neurol. 2005;95:59-70. Adv Neurol. 2005. PMID: 15508914 Review. No abstract available.
Electroclinical findings in four patients with karyotype 47,XYY.
Torniero C, Bernardina BD, Fontana E, Darra F, Danesino C, Elia M. Torniero C, et al. Among authors: fontana e. Brain Dev. 2011 May;33(5):384-9. doi: 10.1016/j.braindev.2010.07.010. Epub 2010 Sep 16. Brain Dev. 2011. PMID: 20817432
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.
Ragona F, Granata T, Dalla Bernardina B, Offredi F, Darra F, Battaglia D, Morbi M, Brazzo D, Cappelletti S, Chieffo D, De Giorgi I, Fontana E, Freri E, Marini C, Toraldo A, Specchio N, Veggiotti P, Vigevano F, Guerrini R, Guzzetta F, Dravet C. Ragona F, et al. Among authors: fontana e. Epilepsia. 2011 Feb;52(2):386-92. doi: 10.1111/j.1528-1167.2010.02925.x. Epub 2011 Jan 26. Epilepsia. 2011. PMID: 21269283 Free article.
334 results