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Page 1
DPP6 gene disruption in a family with Gilles de la Tourette syndrome.
Prontera P, Napolioni V, Ottaviani V, Rogaia D, Fusco C, Augello B, Serino D, Parisi V, Bernardini L, Merla G, Cavanna AE, Donti E. Prontera P, et al. Among authors: serino d. Neurogenetics. 2014 Oct;15(4):237-42. doi: 10.1007/s10048-014-0418-9. Epub 2014 Aug 17. Neurogenetics. 2014. PMID: 25129042
Epilepsy in patients with duplications of chromosome 14 harboring FOXG1.
Pontrelli G, Cappelletti S, Claps D, Sirleto P, Ciocca L, Petrocchi S, Terracciano A, Serino D, Fusco L, Vigevano F, Specchio N. Pontrelli G, et al. Among authors: serino d. Pediatr Neurol. 2014 May;50(5):530-5. doi: 10.1016/j.pediatrneurol.2014.01.022. Epub 2014 Jan 11. Pediatr Neurol. 2014. PMID: 24731847 Review.
Evaluation of BRAF, RAS, RET/PTC, and PAX8/PPARg alterations in different Bethesda diagnostic categories: A multicentric prospective study on the validity of the 7-gene panel test in 1172 thyroid FNAs deriving from different hospitals in South Italy.
Bellevicine C, Migliatico I, Sgariglia R, Nacchio M, Vigliar E, Pisapia P, Iaccarino A, Bruzzese D, Fonderico F, Salvatore D, Biondi B, Masone S, Novizio V, Scavuzzo F, Serino D, De Palma M, Chiofalo MG, Botti G, Pezzullo L, Nuzzo V, Spiezia S, De Chiara G, Iorio S, Conzo G, Docimo G, Faggiano A, Bongiovanni M, Malapelle U, Colao A, Triassi M, Troncone G; Tiroide Network. Bellevicine C, et al. Among authors: serino d. Cancer Cytopathol. 2020 Feb;128(2):107-118. doi: 10.1002/cncy.22217. Epub 2019 Dec 10. Cancer Cytopathol. 2020. PMID: 31821746 Free article.
Epilepsy in KBG syndrome.
Auconi M, Serino D, Digilio MC, Gnazzo M, Conti M, Vigevano F, Fusco L. Auconi M, et al. Among authors: serino d. Dev Med Child Neurol. 2023 May;65(5):712-720. doi: 10.1111/dmcn.15428. Epub 2022 Oct 4. Dev Med Child Neurol. 2023. PMID: 36196002 Free article.
37 results