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Page 1
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome.
Masnada S, Pichiecchio A, Formica M, Arrigoni F, Borrelli P, Accorsi P, Bonanni P, Borgatti R, Bernardina BD, Danieli A, Darra F, Deconinck N, De Giorgis V, Dulac O, Gataullina S, Giordano L, Guerrini R, La Briola F, Mastrangelo M, Montomoli M, Mortilla M, Osanni E, Parisi P, Perucca E, Pinelli L, Romaniello R, Severino M, Vigevano F, Vignoli A, Bahi-Buisson N, Cavallin M, Accogli A, Burgeois M, Capra V, Chaves-Vischer V, Chiapparini L, Colafati G, D'Arrigo S, Desguerre I, Doco-Fenzy M, d'Orsi G, Epitashvili N, Fazzi E, Ferretti A, Fiorini E, Fradin M, Fusco C, Granata T, Johannesen KM, Lebon S, Loget P, Moller RS, Montanaro D, Orcesi S, Quelin C, Rebessi E, Romeo A, Solazzi R, Spagnoli C, Uebler C, Zara F, Arzimanoglou A, Veggiotti P; Aicardi Syndrome International Study Group. Masnada S, et al. Among authors: spagnoli c. Neurology. 2021 Mar 2;96(9):e1319-e1333. doi: 10.1212/WNL.0000000000011237. Epub 2020 Dec 4. Neurology. 2021. PMID: 33277420 Free PMC article.
KCNQ2 encephalopathy: A case due to a de novo deletion.
Spagnoli C, Salerno GG, Iodice A, Frattini D, Pisani F, Fusco C. Spagnoli C, et al. Brain Dev. 2018 Jan;40(1):65-68. doi: 10.1016/j.braindev.2017.06.008. Epub 2017 Jul 17. Brain Dev. 2018. PMID: 28728838
Corticosteroid treatment in Sydenham's chorea.
Fusco C, Spagnoli C. Fusco C, et al. Among authors: spagnoli c. Eur J Paediatr Neurol. 2018 Mar;22(2):327-331. doi: 10.1016/j.ejpn.2017.11.011. Epub 2017 Dec 16. Eur J Paediatr Neurol. 2018. PMID: 29287833
HCN1 mutation spectrum: from neonatal epileptic encephalopathy to benign generalized epilepsy and beyond.
Marini C, Porro A, Rastetter A, Dalle C, Rivolta I, Bauer D, Oegema R, Nava C, Parrini E, Mei D, Mercer C, Dhamija R, Chambers C, Coubes C, Thévenon J, Kuentz P, Julia S, Pasquier L, Dubourg C, Carré W, Rosati A, Melani F, Pisano T, Giardino M, Innes AM, Alembik Y, Scheidecker S, Santos M, Figueiroa S, Garrido C, Fusco C, Frattini D, Spagnoli C, Binda A, Granata T, Ragona F, Freri E, Franceschetti S, Canafoglia L, Castellotti B, Gellera C, Milanesi R, Mancardi MM, Clark DR, Kok F, Helbig KL, Ichikawa S, Sadler L, Neupauerová J, Laššuthova P, Šterbová K, Laridon A, Brilstra E, Koeleman B, Lemke JR, Zara F, Striano P, Soblet J, Smits G, Deconinck N, Barbuti A, DiFrancesco D, LeGuern E, Guerrini R, Santoro B, Hamacher K, Thiel G, Moroni A, DiFrancesco JC, Depienne C. Marini C, et al. Among authors: spagnoli c. Brain. 2018 Nov 1;141(11):3160-3178. doi: 10.1093/brain/awy263. Brain. 2018. PMID: 30351409 Free article.
Restless Legs Syndrome in NKX2-1-related chorea: An expansion of the disease spectrum.
Iodice A, Carecchio M, Zorzi G, Garavaglia B, Spagnoli C, Salerno GG, Frattini D, Mencacci NE, Invernizzi F, Veneziano L, Mantuano E, Angriman M, Fusco C. Iodice A, et al. Among authors: spagnoli c. Brain Dev. 2019 Mar;41(3):250-256. doi: 10.1016/j.braindev.2018.10.001. Epub 2018 Oct 21. Brain Dev. 2019. PMID: 30352709
New biallelic GBA2 variant in a patient with SPG46.
Spagnoli C, Schiavoni S, Rizzi S, Salerno GG, Frattini D, Fusco C. Spagnoli C, et al. Clin Neurol Neurosurg. 2020 Apr;191:105676. doi: 10.1016/j.clineuro.2020.105676. Epub 2020 Jan 13. Clin Neurol Neurosurg. 2020. PMID: 31955126 No abstract available.
EEG Monitoring of the Epileptic Newborn.
Pisani F, Spagnoli C, Fusco C. Pisani F, et al. Among authors: spagnoli c. Curr Neurol Neurosci Rep. 2020 Mar 12;20(4):6. doi: 10.1007/s11910-020-1027-7. Curr Neurol Neurosci Rep. 2020. PMID: 32166392 Review.
130 results