Coppola A - Search Results

1

Epilepsy in Rett Syndrome: can seizures play an encephalopathic effect in this disorder?

Bernardo P, Coppola A, Terrone G, Riccio MP, Santoro C, Del Giudice E, Bravaccio C. Bernardo P, et al. Among authors: coppola a. Minerva Pediatr. 2019 Aug;71(4):391-393. doi: 10.23736/S0026-4946.19.05309-X. Epub 2019 Apr 5. Minerva Pediatr. 2019. PMID: 30961341 No abstract available.

2

17q21.31 microdeletion syndrome: Description of a case further contributing to the delineation of Koolen-de Vries syndrome.

Bernardo P, Madia F, Santulli L, Del Gaudio L, Caccavale C, Zara F, Traverso M, Cirillo M, Striano S, Coppola A. Bernardo P, et al. Among authors: coppola a. Brain Dev. 2016 Aug;38(7):663-8. doi: 10.1016/j.braindev.2016.02.002. Epub 2016 Feb 17. Brain Dev. 2016. PMID: 26897099

3

CHD2 mutations: Only epilepsy? Description of cognitive and behavioral profile in a case with a new mutation.

Bernardo P, Galletta D, Iasevoli F, D'Ambrosio L, Troisi S, Gennaro E, Zara F, Striano S, de Bartolomeis A, Coppola A. Bernardo P, et al. Among authors: coppola a. Seizure. 2017 Oct;51:186-189. doi: 10.1016/j.seizure.2017.09.001. Epub 2017 Sep 6. Seizure. 2017. PMID: 28910737 Free article. No abstract available.

4

Seizures in children with neurofibromatosis type 1: is neurofibromatosis type 1 enough?

Santoro C, Bernardo P, Coppola A, Pugliese U, Cirillo M, Giugliano T, Piluso G, Cinalli G, Striano S, Bravaccio C, Perrotta S. Santoro C, et al. Among authors: coppola a. Ital J Pediatr. 2018 Mar 22;44(1):41. doi: 10.1186/s13052-018-0477-x. Ital J Pediatr. 2018. PMID: 29566708 Free PMC article.

5

High-functioning autism spectrum disorder with fluent speech and late-onset epilepsy: an unusual presentation of Inv-Dup (15) syndrome.

Bernardo P, Del Gaudio L, Madia F, Riccio MP, Marino M, Santoro C, Caccavale C, Striano S, Bravaccio C, Coppola A. Bernardo P, et al. Among authors: coppola a. Neurocase. 2019 Feb-Apr;25(1-2):62-65. doi: 10.1080/13554794.2019.1602144. Epub 2019 Apr 16. Neurocase. 2019. PMID: 30991884

6

Clinical evolution and epilepsy outcome in three patients with CDKL5-related developmental encephalopathy.

Bernardo P, Ferretti A, Terrone G, Santoro C, Bravaccio C, Striano S, Coppola A, Striano P. Bernardo P, et al. Among authors: coppola a. Epileptic Disord. 2019 Jun 1;21(3):271-277. doi: 10.1684/epd.2019.1071. Epileptic Disord. 2019. PMID: 31225800

7

Consolidating the Role of TDP2 Mutations in Recessive Spinocerebellar Ataxia Associated with Pediatric Onset Drug Resistant Epilepsy and Intellectual Disability (SCAR23).

Ciaccio C, Castello R, Esposito S, Pinelli M, Nigro V, Casari G, Chiapparini L, Pantaleoni C; TUDP Study Group; D'Arrigo S. Ciaccio C, et al. Cerebellum. 2019 Oct;18(5):972-975. doi: 10.1007/s12311-019-01069-7. Cerebellum. 2019. PMID: 31410782

8

Xq25 microduplication syndrome: a further contribution to its definition. A case report and review of the literature.

Turchi G, Bernardo P, Consales A, Bilo L, Coppola A. Turchi G, et al. Among authors: coppola a. Clin Dysmorphol. 2020 Apr;29(2):90-96. doi: 10.1097/MCD.0000000000000303. Clin Dysmorphol. 2020. PMID: 31609727 Review. No abstract available.

9

Neurophysiological Signatures of Motor Impairment in Patients with Rett Syndrome.

Bernardo P, Cobb S, Coppola A, Tomasevic L, Di Lazzaro V, Bravaccio C, Manganelli F, Dubbioso R. Bernardo P, et al. Among authors: coppola a. Ann Neurol. 2020 May;87(5):763-773. doi: 10.1002/ana.25712. Epub 2020 Mar 17. Ann Neurol. 2020. PMID: 32129908

10

Dual diagnosis in a child with familial SCN8A-related encephalopathy complicated by a 1p13.2 deletion involving NRAS gene.

Alagia M, Bernardo P, Genesio R, Gennaro E, Brunetti-Pierri N, Coppola A, Zara F, Striano P, Striano S, Terrone G. Alagia M, et al. Among authors: coppola a. Neurol Sci. 2021 May;42(5):2115-2117. doi: 10.1007/s10072-020-04898-1. Epub 2020 Nov 17. Neurol Sci. 2021. PMID: 33201365 No abstract available.

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