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2017 1
2020 1
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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: troisi s. 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.
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. Among authors: troisi s. Brain Sci. 2020 Aug 1;10(8):506. doi: 10.3390/brainsci10080506. Brain Sci. 2020. PMID: 32752208 Free PMC article.