Musumeci SA - Search Results

1

A new family with periventricular nodular heterotopia and peculiar dysmorphic features. A probable X-linked dominant trait.

Musumeci SA, Ferri R, Elia M, Scuderi C, Del Gracco S, Azan G, Stefanini MC. Musumeci SA, et al. Arch Neurol. 1997 Jan;54(1):61-4. doi: 10.1001/archneur.1997.00550130045014. Arch Neurol. 1997. PMID: 9006415

2

Clinical and neurophysiological aspects of epilepsy in subjects with autism and mental retardation.

Elia M, Musumeci SA, Ferri R, Bergonzi P. Elia M, et al. Among authors: musumeci sa. Am J Ment Retard. 1995 Jul;100(1):6-16. Am J Ment Retard. 1995. PMID: 7546638

3

Saethre-Chotzen syndrome: a clinical, EEG and neuroradiological study.

Elia M, Musumeci SA, Ferri R, Greco D, Romano C, Del Gracco S, Stefanini MC. Elia M, et al. Among authors: musumeci sa. Childs Nerv Syst. 1996 Nov;12(11):699-704. doi: 10.1007/BF00366154. Childs Nerv Syst. 1996. PMID: 9118134

4

Familial cortical tremor, epilepsy, and mental retardation: a distinct clinical entity?

Elia M, Musumeci SA, Ferri R, Scuderi C, Del Gracco S, Bottitta M, Michelucci R, Tassinari CA. Elia M, et al. Among authors: musumeci sa. Arch Neurol. 1998 Dec;55(12):1569-73. doi: 10.1001/archneur.55.12.1569. Arch Neurol. 1998. PMID: 9865802

5

Eyelid myoclonia with absences in three subjects with mental retardation.

Scuderi C, Musumeci SA, Ferri R, Calabrese G, Elia M. Scuderi C, et al. Among authors: musumeci sa. Neurol Sci. 2000 Aug;21(4):247-50. doi: 10.1007/s100720070084. Neurol Sci. 2000. PMID: 11214665

6

CDKL5 mutations in boys with severe encephalopathy and early-onset intractable epilepsy.

Elia M, Falco M, Ferri R, Spalletta A, Bottitta M, Calabrese G, Carotenuto M, Musumeci SA, Lo Giudice M, Fichera M. Elia M, et al. Among authors: musumeci sa. Neurology. 2008 Sep 23;71(13):997-9. doi: 10.1212/01.wnl.0000326592.37105.88. Neurology. 2008. PMID: 18809835

7

Does a peculiar EEG pattern exist also for FRAXE mental retardation?

Musumeci SA, Scuderi C, Ferri R, Anello G, Salluzzo R, Bosco P, Elia M. Musumeci SA, et al. Clin Neurophysiol. 2000 Sep;111(9):1632-6. doi: 10.1016/s1388-2457(00)00367-9. Clin Neurophysiol. 2000. PMID: 10964075

8

Audiogenic seizure susceptibility is reduced in fragile X knockout mice after introduction of FMR1 transgenes.

Musumeci SA, Calabrese G, Bonaccorso CM, D'Antoni S, Brouwer JR, Bakker CE, Elia M, Ferri R, Nelson DL, Oostra BA, Catania MV. Musumeci SA, et al. Exp Neurol. 2007 Jan;203(1):233-40. doi: 10.1016/j.expneurol.2006.08.007. Epub 2006 Sep 27. Exp Neurol. 2007. PMID: 17007840

9

Epilepsy and fragile X syndrome: a follow-up study.

Musumeci SA, Ferri R, Elia M, Colognola RM, Bergonzi P, Tassinari CA. Musumeci SA, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):511-3. doi: 10.1002/ajmg.1320380276. Am J Med Genet. 1991. PMID: 2018098

10

Seizures in Klinefelter's syndrome: a clinical and EEG study of five patients.

Elia M, Musumeci SA, Ferri R, Scuderi C, Del Gracco S, Stefanini MC. Elia M, et al. Among authors: musumeci sa. Ital J Neurol Sci. 1995 May;16(4):231-8. doi: 10.1007/BF02282994. Ital J Neurol Sci. 1995. PMID: 7591675

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