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GABRA1-Related Disorders: From Genetic to Functional Pathways.
Musto E, Liao VWY, Johannesen KM, Fenger CD, Lederer D, Kothur K, Fisk K, Bennetts B, Vrielynck P, Delaby D, Ceulemans B, Weckhuysen S, Sparber P, Bouman A, Ardern-Holmes S, Troedson C, Battaglia DI, Goel H, Feyma T, Bakhtiari S, Tjoa L, Boxill M, Demina N, Shchagina O, Dadali E, Kruer M, Cantalupo G, Contaldo I, Polster T, Isidor B, Bova SM, Fazeli W, Wouters L, Miranda MJ, Darra F, Pede E, Le Duc D, Jamra RA, Küry S, Proietti J, McSweeney N, Brokamp E, Andrews PI, Gouray Garcia M, Chebib M, Møller RS, Ahring PK, Gardella E. Musto E, et al. Among authors: contaldo i. Ann Neurol. 2023 Aug 22. doi: 10.1002/ana.26774. Online ahead of print. Ann Neurol. 2023. PMID: 37606373
Cognitive decline in Dravet syndrome: is there a cerebellar role?
Battaglia D, Chieffo D, Siracusano R, Waure Cd, Brogna C, Ranalli D, Contaldo I, Tortorella G, Dravet C, Mercuri E, Guzzetta F. Battaglia D, et al. Among authors: contaldo i. Epilepsy Res. 2013 Sep;106(1-2):211-21. doi: 10.1016/j.eplepsyres.2013.03.012. Epub 2013 Apr 30. Epilepsy Res. 2013. PMID: 23642572
Surgery for posterior quadrantic cortical dysplasia. A review.
Tamburrini G, Battaglia D, Albamonte E, Contaldo I, Massimi L, Caldarelli M, Di Rocco C. Tamburrini G, et al. Among authors: contaldo i. Childs Nerv Syst. 2014 Nov;30(11):1859-68. doi: 10.1007/s00381-014-2449-9. Epub 2014 Oct 9. Childs Nerv Syst. 2014. PMID: 25296547 Review.
Cognitive-behavioral profiles in teenagers with Dravet syndrome.
Olivieri G, Battaglia D, Chieffo D, Rubbino R, Ranalli D, Contaldo I, Dravet C, Mercuri E, Guzzetta F. Olivieri G, et al. Among authors: contaldo i. Brain Dev. 2016 Jun;38(6):554-62. doi: 10.1016/j.braindev.2015.12.014. Epub 2016 Jan 18. Brain Dev. 2016. PMID: 26797655
Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations.
Cetica V, Chiari S, Mei D, Parrini E, Grisotto L, Marini C, Pucatti D, Ferrari A, Sicca F, Specchio N, Trivisano M, Battaglia D, Contaldo I, Zamponi N, Petrelli C, Granata T, Ragona F, Avanzini G, Guerrini R. Cetica V, et al. Among authors: contaldo i. Neurology. 2017 Mar 14;88(11):1037-1044. doi: 10.1212/WNL.0000000000003716. Epub 2017 Feb 15. Neurology. 2017. PMID: 28202706 Free PMC article.
Heart rate variability alterations in Dravet Syndrome: The role of status epilepticus and a possible association with mortality risk.
Perulli M, Battista A, Sivo S, Turrini I, Musto E, Quintiliani M, Gambardella ML, Contaldo I, Veredice C, Mercuri EM, Lanza GA, Dravet C, Delogu AB, Battaglia DI. Perulli M, et al. Among authors: contaldo i. Seizure. 2022 Jan;94:129-135. doi: 10.1016/j.seizure.2021.11.023. Epub 2021 Nov 27. Seizure. 2022. PMID: 34896816 Free article.
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: contaldo i. Front Neurol. 2022 Jan 26;12:805745. doi: 10.3389/fneur.2021.805745. eCollection 2021. Front Neurol. 2022. PMID: 35153983 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: contaldo i. J Clin Med. 2022 Oct 20;11(20):6182. doi: 10.3390/jcm11206182. J Clin Med. 2022. PMID: 36294502 Free PMC article.
40 results