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Page 1
Electroencephalographic and epileptic patterns in X chromosome anomalies.
Grosso S, Farnetani MA, Di Bartolo RM, Berardi R, Pucci L, Mostardini R, Anichini C, Bartalini G, Galimberti D, Morgese G, Balestri P. Grosso S, et al. Among authors: berardi r. J Clin Neurophysiol. 2004 Jul-Aug;21(4):249-53. doi: 10.1097/00004691-200407000-00003. J Clin Neurophysiol. 2004. PMID: 15509914
Medial temporal lobe dysgenesis in Muenke syndrome and hypochondroplasia.
Grosso S, Farnetani MA, Berardi R, Bartalini G, Carpentieri M, Galluzzi P, Mostardini R, Morgese G, Balestri P. Grosso S, et al. Among authors: berardi r. Am J Med Genet A. 2003 Jul 1;120A(1):88-91. doi: 10.1002/ajmg.a.10171. Am J Med Genet A. 2003. PMID: 12794698
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: berardi r. 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
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: berardi r. 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
637 results