Elia M - Search Results

1

Transient Brain Lesions in Neuro-Behçet's Disease without Systemic Involvement.

Amato C, Elia M. Amato C, et al. Among authors: elia m. Neuroradiol J. 2012 Jul;25(3):319-24. doi: 10.1177/197140091202500306. Epub 2012 Jun 26. Neuroradiol J. 2012. PMID: 24028984

2

Transient MRI abnormalities associated with partial status epilepticus: a case report.

Amato C, Elia M, Musumeci SA, Bisceglie P, Moschini M. Amato C, et al. Among authors: elia m. Eur J Radiol. 2001 Apr;38(1):50-4. doi: 10.1016/s0720-048x(00)00284-9. Eur J Radiol. 2001. PMID: 11287165

3

Nervous system involvement in Degos disease.

Amato C, Ferri R, Elia M, Cosentino F, Schepis C, Siragusa M, Moschini M. Amato C, et al. Among authors: elia m. AJNR Am J Neuroradiol. 2005 Mar;26(3):646-9. AJNR Am J Neuroradiol. 2005. PMID: 15760880 Free PMC article.

4

6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.

Elia M, Striano P, Fichera M, Gaggero R, Castiglia L, Galesi O, Malacarne M, Pierluigi M, Amato C, Musumeci SA, Romano C, Majore S, Grammatico P, Zara F, Striano S, Faravelli F. Elia M, et al. Epilepsia. 2006 May;47(5):830-8. doi: 10.1111/j.1528-1167.2006.00522.x. Epilepsia. 2006. PMID: 16686647 Free article.

5

Nail aplasia, microcephaly, severe mental retardation and MRI abnormalities: report of two unrelated cases.

Musumeci SA, Elia M, Fichera M, Amato C, Ferri R, Romano C, Federico A. Musumeci SA, et al. Among authors: elia m. Neurol Sci. 2006 Dec;27(6):425-31. doi: 10.1007/s10072-006-0724-6. Neurol Sci. 2006. PMID: 17205229

6

Posterior fossa abnormalities in hereditary spastic paraparesis with spastin mutations.

Scuderi C, Fichera M, Calabrese G, Elia M, Amato C, Savio M, Borgione E, Vitello GA, Musumeci SA. Scuderi C, et al. Among authors: elia m. J Neurol Neurosurg Psychiatry. 2009 Apr;80(4):440-3. doi: 10.1136/jnnp.2008.154807. J Neurol Neurosurg Psychiatry. 2009. PMID: 19289482

7

Schimmelpenning syndrome: a kind of craniofacial epidermal nevus associated with cerebral and ocular MR imaging abnormalities.

Amato C, Elia M, Schepis C. Amato C, et al. Among authors: elia m. AJNR Am J Neuroradiol. 2010 May;31(5):E47-8. doi: 10.3174/ajnr.A2062. Epub 2010 Mar 18. AJNR Am J Neuroradiol. 2010. PMID: 20299435 Free PMC article. No abstract available.

8

Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortex.

Scuderi C, Borgione E, Castello F, Lo Giudice M, Fichera M, Elia M, Amato C, Savio M, Di Blasi FD, Vitello GA, Romano S, DiMauro S, Musumeci SA. Scuderi C, et al. Among authors: elia m. Mitochondrion. 2010 Aug;10(5):548-54. doi: 10.1016/j.mito.2010.04.004. Epub 2010 Apr 28. Mitochondrion. 2010. PMID: 20433951

9

An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy.

Elia M, Amato C, Bottitta M, Grillo L, Calabrese G, Esposito M, Carotenuto M. Elia M, et al. Brain Dev. 2012 Nov;34(10):873-6. doi: 10.1016/j.braindev.2012.03.005. Epub 2012 Apr 1. Brain Dev. 2012. PMID: 22469695

10

Tuberous sclerosis underlying neonatal poliosis.

Schepis C, Siragusa M, Puzzo A, Amato C, Elia M. Schepis C, et al. Among authors: elia m. J Eur Acad Dermatol Venereol. 2015 Apr;29(4):822-3. doi: 10.1111/jdv.12427. Epub 2014 Mar 5. J Eur Acad Dermatol Venereol. 2015. PMID: 24593831 No abstract available.

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