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A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3.
Mastrangelo M, Mei D, Cesario S, Fioriello F, Bernardini L, Brinciotti M, Guerrini R, Leuzzi V. Mastrangelo M, et al. Among authors: brinciotti m. Parkinsonism Relat Disord. 2019 Nov;68:1-3. doi: 10.1016/j.parkreldis.2019.09.016. Epub 2019 Sep 18. Parkinsonism Relat Disord. 2019. PMID: 31621611 No abstract available.
Familial occurrence of benign myoclonus of early infancy.
Galletti F, Brinciotti M, Emanuelli O. Galletti F, et al. Among authors: brinciotti m. Epilepsia. 1989 Sep-Oct;30(5):579-81. doi: 10.1111/j.1528-1157.1989.tb05475.x. Epilepsia. 1989. PMID: 2507303
Long-term outcome of pattern-sensitive epilepsy.
Brinciotti M, Matricardi M, Cantonetti L, Lauretti G, Pugliatti M. Brinciotti M, et al. Epilepsia. 2006;47 Suppl 5:36-40. doi: 10.1111/j.1528-1167.2006.00875.x. Epilepsia. 2006. PMID: 17239104 Free article.
Self-induced pattern-sensitive epilepsy in childhood.
Matricardi M, Brinciotti M, Trasatti G, Porro G. Matricardi M, et al. Among authors: brinciotti m. Acta Paediatr Scand. 1990 Feb;79(2):237-40. doi: 10.1111/j.1651-2227.1990.tb11448.x. Acta Paediatr Scand. 1990. PMID: 2108529
Epilepsy phenotype in patients with Xp22.31 microduplication.
Brinciotti M, Fioriello F, Mittica A, Bernardini L, Goldoni M, Matricardi M. Brinciotti M, et al. Epilepsy Behav Case Rep. 2018 Nov 4;11:31-34. doi: 10.1016/j.ebcr.2018.10.004. eCollection 2019. Epilepsy Behav Case Rep. 2018. PMID: 30603611 Free PMC article.
[Continuous localized EEG discharges during sleep in children].
Pelliccia A, Galletti F, Pierantoni R, Gulotta E, Ferrara M, Brinciotti M, Benedetti P. Pelliccia A, et al. Among authors: brinciotti m. Neurophysiol Clin. 1989 May;19(2):145-54. doi: 10.1016/s0987-7053(89)80054-1. Neurophysiol Clin. 1989. PMID: 2498627 French.
40 results