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Ohtahara syndrome with emphasis on recent genetic discovery.
Pavone P, Spalice A, Polizzi A, Parisi P, Ruggieri M. Pavone P, et al. Among authors: parisi p. Brain Dev. 2012 Jun;34(6):459-68. doi: 10.1016/j.braindev.2011.09.004. Epub 2011 Oct 2. Brain Dev. 2012. PMID: 21967765 Review.
Neuronal heterotopia.
Iannetti P, Spalice A, Raucci U, Parisi P. Iannetti P, et al. Among authors: parisi p. Neurology. 1995 Oct;45(10):1945-6. doi: 10.1212/wnl.45.10.1945. Neurology. 1995. PMID: 7478004 No abstract available.
Efficacy and safety of topiramate in refractory epilepsy of childhood: long-term follow-up study.
Grosso S, Franzoni E, Iannetti P, Incorpora G, Cardinali C, Toldo I, Verrotti A, Caterina Moscano F, Lo Faro V, Mazzone L, Zamponi N, Boniver C, Spalice A, Parisi P, Morgese G, Balestri P. Grosso S, et al. Among authors: parisi p. J Child Neurol. 2005 Nov;20(11):893-7. doi: 10.1177/08830738050200110601. J Child Neurol. 2005. PMID: 16417859 Clinical Trial.
Bilateral perysilvian polymicrogyria in Chiari I malformation.
Spalice A, Parisi P, Mastrangelo M, De Luca F, Verrotti A, Iannetti P. Spalice A, et al. Among authors: parisi p. Childs Nerv Syst. 2006 Dec;22(12):1635-7. doi: 10.1007/s00381-006-0180-x. Epub 2006 Oct 13. Childs Nerv Syst. 2006. PMID: 17058087
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders.
Brancati F, Travaglini L, Zablocka D, Boltshauser E, Accorsi P, Montagna G, Silhavy JL, Barrano G, Bertini E, Emma F, Rigoli L; International JSRD Study Group; Dallapiccola B, Gleeson JG, Valente EM. Brancati F, et al. Clin Genet. 2008 Aug;74(2):164-70. doi: 10.1111/j.1399-0004.2008.01047.x. Epub 2008 Jun 28. Clin Genet. 2008. PMID: 18565097 Free PMC article.
407 results