Amato C - Search Results

1

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: amato c. J Neurol Neurosurg Psychiatry. 2009 Apr;80(4):440-3. doi: 10.1136/jnnp.2008.154807. J Neurol Neurosurg Psychiatry. 2009. PMID: 19289482

2

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: amato c. Mitochondrion. 2010 Aug;10(5):548-54. doi: 10.1016/j.mito.2010.04.004. Epub 2010 Apr 28. Mitochondrion. 2010. PMID: 20433951

3

The in cis T251I and P587L POLG1 base changes: description of a new family and literature review.

Scuderi C, Borgione E, Castello F, Lo Giudice M, Santa Paola S, Giambirtone M, Di Blasi FD, Elia M, Amato C, Città S, Gagliano C, Barbarino G, Vitello GA, Musumeci SA. Scuderi C, et al. Among authors: amato c. Neuromuscul Disord. 2015 Apr;25(4):333-9. doi: 10.1016/j.nmd.2015.01.004. Epub 2015 Jan 19. Neuromuscul Disord. 2015. PMID: 25660390 Review.

4

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: amato c. Neurol Sci. 2006 Dec;27(6):425-31. doi: 10.1007/s10072-006-0724-6. Neurol Sci. 2006. PMID: 17205229

5

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. Among authors: amato c. Epilepsia. 2006 May;47(5):830-8. doi: 10.1111/j.1528-1167.2006.00522.x. Epilepsia. 2006. PMID: 16686647 Free article.

6

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. Eur J Radiol. 2001 Apr;38(1):50-4. doi: 10.1016/s0720-048x(00)00284-9. Eur J Radiol. 2001. PMID: 11287165

7

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

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

8

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. Among authors: amato c. 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

9

Long faun tail: a rare cutaneous marker of spinal dysraphism.

Schepis C, Elia M, Amato C. Schepis C, et al. Among authors: amato c. G Ital Dermatol Venereol. 2016 Oct;151(5):572-4. Epub 2015 Sep 16. G Ital Dermatol Venereol. 2016. PMID: 26376040 No abstract available.

10

Nervous system involvement in Degos disease.

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

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