Coppola A - Search Results

1

Diagnosis and Management of Type 1 Sialidosis: Clinical Insights from Long-Term Care of Four Unrelated Patients.

Coppola A, Ianniciello M, Vanli-Yavuz EN, Rossi S, Simonelli F, Castellotti B, Esposito M, Tozza S, Troisi S, Bellofatto M, Ugga L, Striano S, D'Amico A, Baykan B, Striano P, Bilo L. Coppola A, et al. Brain Sci. 2020 Aug 1;10(8):506. doi: 10.3390/brainsci10080506. Brain Sci. 2020. PMID: 32752208 Free PMC article.

2

Levetiracetam for cerebellar tremor in multiple sclerosis: an open-label pilot tolerability and efficacy study.

Striano P, Coppola A, Vacca G, Zara F, Brescia Morra V, Orefice G, Striano S. Striano P, et al. Among authors: coppola a. J Neurol. 2006 Jun;253(6):762-6. doi: 10.1007/s00415-006-0112-4. Epub 2006 May 12. J Neurol. 2006. PMID: 16683063

3

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases.

Striano P, Malacarne M, Cavani S, Pierluigi M, Rinaldi R, Cavaliere ML, Rinaldi MM, De Bernardo C, Coppola A, Pintaudi M, Gaggero R, Grammatico P, Striano S, Dallapiccola B, Zara F, Faravelli F. Striano P, et al. Among authors: coppola a. Am J Med Genet A. 2006 Sep 15;140(18):1944-9. doi: 10.1002/ajmg.a.31435. Am J Med Genet A. 2006. PMID: 16906558

4

Inherited neuromyotonia: a clinical and genetic study of a family.

Falace A, Striano P, Manganelli F, Coppola A, Striano S, Minetti C, Zara F. Falace A, et al. Among authors: coppola a. Neuromuscul Disord. 2007 Jan;17(1):23-7. doi: 10.1016/j.nmd.2006.09.014. Epub 2006 Nov 30. Neuromuscul Disord. 2007. PMID: 17140792

5

Life-threatening status epilepticus following gabapentin administration in a patient with benign adult familial myoclonic epilepsy.

Striano P, Coppola A, Madia F, Pezzella M, Ciampa C, Zara F, Striano S. Striano P, et al. Among authors: coppola a. Epilepsia. 2007 Oct;48(10):1995-8. doi: 10.1111/j.1528-1167.2007.01198.x. Epub 2007 Jul 21. Epilepsia. 2007. PMID: 17645541 Free article.

6

Familial mesial temporal lobe epilepsy (FMTLE) : a clinical and genetic study of 15 Italian families.

Striano P, Gambardella A, Coppola A, Di Bonaventura C, Bovo G, Diani E, Boaretto F, Egeo G, Ciampa C, Labate A, Testoni S, Passarelli D, Manna I, Sferro C, Aguglia U, Caranci F, Giallonardo AT, Striano S, Nobile C, Michelucci R. Striano P, et al. Among authors: coppola a. J Neurol. 2008 Jan;255(1):16-23. doi: 10.1007/s00415-007-0653-1. Epub 2007 Nov 21. J Neurol. 2008. PMID: 18004642

7

A pilot trial of levetiracetam in eyelid myoclonia with absences (Jeavons syndrome).

Striano P, Sofia V, Capovilla G, Rubboli G, Di Bonaventura C, Coppola A, Vitale G, Fontanillas L, Giallonardo AT, Biondi R, Romeo A, Viri M, Zara F, Striano S. Striano P, et al. Among authors: coppola a. Epilepsia. 2008 Mar;49(3):425-30. doi: 10.1111/j.1528-1167.2007.01524.x. Epub 2008 Jan 29. Epilepsia. 2008. PMID: 18248445 Free article. Clinical Trial.

8

A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms.

Coppola A, Striano P, Gimelli S, Ciampa C, Santulli L, Caranci F, Zuffardi O, Gimelli G, Striano S, Zara F. Coppola A, et al. Brain Dev. 2010 Mar;32(3):248-52. doi: 10.1016/j.braindev.2009.01.003. Epub 2009 Feb 11. Brain Dev. 2010. PMID: 19216040

9

The syndrome gelastic seizures-hypothalamic hamartoma: severe, potentially reversible encephalopathy.

Striano S, Striano P, Coppola A, Romanelli P. Striano S, et al. Among authors: coppola a. Epilepsia. 2009 May;50 Suppl 5:62-5. doi: 10.1111/j.1528-1167.2009.02125.x. Epilepsia. 2009. PMID: 19469851 Free article. Review.

10

A pilot open-label trial of zonisamide in Unverricht-Lundborg disease.

Italiano D, Pezzella M, Coppola A, Magaudda A, Ferlazzo E, Bramanti P, Striano S, Zara F, Striano P. Italiano D, et al. Among authors: coppola a. Mov Disord. 2011 Feb 1;26(2):341-3. doi: 10.1002/mds.23392. Epub 2010 Oct 11. Mov Disord. 2011. PMID: 20939070

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