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201 results

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Page 1
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform.
Della Mina E, Ciccone R, Brustia F, Bayindir B, Limongelli I, Vetro A, Iascone M, Pezzoli L, Bellazzi R, Perotti G, De Giorgis V, Lunghi S, Coppola G, Orcesi S, Merli P, Savasta S, Veggiotti P, Zuffardi O. Della Mina E, et al. Among authors: savasta s. Eur J Hum Genet. 2015 Mar;23(3):354-62. doi: 10.1038/ejhg.2014.92. Epub 2014 May 21. Eur J Hum Genet. 2015. PMID: 24848745 Free PMC article.
Ehlers-Danlos syndrome and neurological features: a review.
Savasta S, Merli P, Ruggieri M, Bianchi L, Spartà MV. Savasta S, et al. Childs Nerv Syst. 2011 Mar;27(3):365-71. doi: 10.1007/s00381-010-1256-1. Epub 2010 Aug 10. Childs Nerv Syst. 2011. PMID: 20697718 Review.
Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndrome.
Verrotti A, Cusmai R, Nicita F, Pizzolorusso A, Elia M, Zamponi N, Cesaroni E, Granata T, De Giorgi I, Giordano L, Grosso S, Pavone P, Franzoni E, Coppola G, Cerminara C, Curatolo P, Savasta S, Striano P, Parisi P, Romeo A, Spalice A. Verrotti A, et al. Among authors: savasta s. J Pediatr. 2013 Dec;163(6):1754-8. doi: 10.1016/j.jpeds.2013.07.022. Epub 2013 Aug 27. J Pediatr. 2013. PMID: 23992680
Long-term follow-up in children with benign convulsions associated with gastroenteritis.
Verrotti A, Moavero R, Vigevano F, Cantonetti L, Guerra A, Spezia E, Tricarico A, Nanni G, Agostinelli S, Chiarelli F, Parisi P, Capovilla G, Beccaria F, Spalice A, Coppola G, Franzoni E, Gentile V, Casellato S, Veggiotti P, Malgesini S, Crichiutti G, Balestri P, Grosso S, Zamponi N, Incorpora G, Savasta S, Costa P, Pruna D, Cusmai R. Verrotti A, et al. Among authors: savasta s. Eur J Paediatr Neurol. 2014 Sep;18(5):572-7. doi: 10.1016/j.ejpn.2014.04.006. Epub 2014 Apr 14. Eur J Paediatr Neurol. 2014. PMID: 24780603
Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication.
Verrotti A, Laino D, Rinaldi VE, Suppiej A, Giordano L, Toldo I, Margari L, Parisi P, Rizzo R, Matricardi S, Cusmai R, Grosso S, Gaggero R, Zamponi N, Pavone P, Capovilla G, Rauchenzauner M, Cerminara C, Di Gennaro G, Esposito M, Striano P, Savasta S, Coppola G, Siliquini S, Operto F, Belcastro V, Ragona F, Marseglia GL, Spalice A. Verrotti A, et al. Among authors: savasta s. Eur J Neurol. 2016 Feb;23(2):241-6. doi: 10.1111/ene.12840. Epub 2015 Oct 25. Eur J Neurol. 2016. PMID: 26498733
MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome.
Vetro A, Savasta S, Russo Raucci A, Cerqua C, Sartori G, Limongelli I, Forlino A, Maruelli S, Perucca P, Vergani D, Mazzini G, Mattevi A, Stivala LA, Salviati L, Zuffardi O. Vetro A, et al. Among authors: savasta s. Eur J Hum Genet. 2017 May;25(5):646-650. doi: 10.1038/ejhg.2017.5. Epub 2017 Feb 15. Eur J Hum Genet. 2017. PMID: 28198391 Free PMC article.
Electroclinical features of epilepsy monosomy 1p36 syndrome and their implications.
Verrotti A, Greco M, Varriale G, Tamborino A, Savasta S, Carotenuto M, Elia M, Operto F, Margari L, Belcastro V, Selicorni A, Freri E, Matricardi S, Granata T, Ragona F, Capovilla G, Spalice A, Coppola G, Striano P. Verrotti A, et al. Among authors: savasta s. Acta Neurol Scand. 2018 Dec;138(6):523-530. doi: 10.1111/ane.13006. Epub 2018 Aug 14. Acta Neurol Scand. 2018. PMID: 30109707
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study.
Iapadre G, Zagaroli L, Cimini N, Belcastro V, Concolino D, Coppola G, Del Giudice E, Farello G, Iezzi ML, Margari L, Matricardi S, Orsini A, Parisi P, Piccioli M, Di Donato G, Savasta S, Siliquini S, Spalice A, Striano S, Striano P, Verrotti A. Iapadre G, et al. Among authors: savasta s. Epilepsy Behav. 2020 Feb;103(Pt A):106578. doi: 10.1016/j.yebeh.2019.106578. Epub 2019 Nov 1. Epilepsy Behav. 2020. PMID: 31680025
201 results