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Page 1
Epilepsy in neurofibromatosis 1.
Vivarelli R, Grosso S, Calabrese F, Farnetani M, Di Bartolo R, Morgese G, Balestri P. Vivarelli R, et al. Among authors: balestri p. J Child Neurol. 2003 May;18(5):338-42. doi: 10.1177/08830738030180050501. J Child Neurol. 2003. PMID: 12822818
Late-onset childhood occipital epilepsy (Gastaut type): a family study.
Grosso S, Vivarelli R, Gobbi G, Di Bartolo R, Berardi R, Balestri P. Grosso S, et al. Among authors: balestri p. Eur J Paediatr Neurol. 2008 Sep;12(5):421-6. doi: 10.1016/j.ejpn.2007.11.007. Epub 2008 Jan 30. Eur J Paediatr Neurol. 2008. PMID: 18249143
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability.
Mari F, Marozza A, Mencarelli MA, Lo Rizzo C, Fallerini C, Dosa L, Di Marco C, Carignani G, Baldassarri M, Cianci P, Vivarelli R, Vascotto M, Grosso S, Rubegni P, Caffarelli C, Pretegiani E, Fimiani M, Garavelli L, Cristofoli F, Vermeesch JR, Nuti R, Dotti MT, Balestri P, Hayek J, Selicorni A, Renieri A. Mari F, et al. Among authors: balestri p. Brain Dev. 2015 May;37(5):527-36. doi: 10.1016/j.braindev.2014.08.009. Epub 2014 Sep 22. Brain Dev. 2015. PMID: 25249037
Molecular study in von Recklinghausen neurofibromatosis (NF1).
Vivarelli R, Bartalini G, Calistri L, Balestri P, Figus A, Pirastu M, Cao A, Fois A. Vivarelli R, et al. Among authors: balestri p. Childs Nerv Syst. 1991 Apr;7(2):98-9. doi: 10.1007/BF00247864. Childs Nerv Syst. 1991. PMID: 1907526
Malformations of cortical development in neurofibromatosis type 1.
Balestri P, Vivarelli R, Grosso S, Santori L, Farnetani MA, Galluzzi P, Vatti GP, Calabrese F, Morgese G. Balestri P, et al. Neurology. 2003 Dec 23;61(12):1799-801. doi: 10.1212/01.wnl.0000099080.90726.ba. Neurology. 2003. PMID: 14694053
Craniofacial dyssynostosis: case report and review.
Grosso S, Vivarelli R, Muraca MC, Berardi R, Marconcini S, Morgese G, Balestri P. Grosso S, et al. Among authors: balestri p. Am J Med Genet A. 2004 Sep 1;129A(3):300-2. doi: 10.1002/ajmg.a.30186. Am J Med Genet A. 2004. PMID: 15326632
178 results