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Effectiveness of antiepileptic therapy in patients with PCDH19 mutations.
Lotte J, Bast T, Borusiak P, Coppola A, Cross JH, Dimova P, Fogarasi A, Graneß I, Guerrini R, Hjalgrim H, Keimer R, Korff CM, Kurlemann G, Leiz S, Linder-Lucht M, Loddenkemper T, Makowski C, Mühe C, Nicolai J, Nikanorova M, Pellacani S, Philip S, Ruf S, Sánchez Fernández I, Schlachter K, Striano P, Sukhudyan B, Valcheva D, Vermeulen RJ, Weisbrod T, Wilken B, Wolf P, Kluger G. Lotte J, et al. Among authors: coppola a. Seizure. 2016 Feb;35:106-10. doi: 10.1016/j.seizure.2016.01.006. Epub 2016 Jan 6. Seizure. 2016. PMID: 26820223 Free article.
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
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.
Myoclonic epilepsy in a child with 17q22-q23.1 deletion.
Coppola A, Tostevin A, McTague A, Pressler RM, Cross JH, Sisodiya SM. Coppola A, et al. Am J Med Genet A. 2013 Aug;161A(8):2036-9. doi: 10.1002/ajmg.a.36010. Epub 2013 Jun 21. Am J Med Genet A. 2013. PMID: 23794376
998 results