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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1990 1
1992 3
1993 3
1994 2
1995 1
1996 2
1997 4
1998 2
1999 3
2000 1
2001 4
2002 2
2003 10
2004 1
2005 5
2006 7
2007 6
2008 3
2009 7
2010 4
2011 12
2012 7
2013 10
2014 8
2015 7
2016 6
2017 11
2018 12
2019 11
2020 15
2021 17
2022 9
2023 13
2024 9

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198 results

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Page 1
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: granata t. Brain. 2018 Nov 1;141(11):3160-3178. doi: 10.1093/brain/awy263. Brain. 2018. PMID: 30351409 Free article.
Immune-mediated epilepsies.
Granata T, Cross H, Theodore W, Avanzini G. Granata T, et al. Epilepsia. 2011 May;52 Suppl 3(Suppl 3):5-11. doi: 10.1111/j.1528-1167.2011.03029.x. Epilepsia. 2011. PMID: 21542839 Free PMC article. Review.
Rasmussen encephalitis.
Granata T, Andermann F. Granata T, et al. Handb Clin Neurol. 2013;111:511-9. doi: 10.1016/B978-0-444-52891-9.00054-3. Handb Clin Neurol. 2013. PMID: 23622199 Review.
Rasmussen's syndrome.
Granata T. Granata T. Neurol Sci. 2003 Oct;24 Suppl 4:S239-43. doi: 10.1007/s10072-003-0086-2. Neurol Sci. 2003. PMID: 14598051 Review.
Schizencephaly.
Granata T, Battaglia G. Granata T, et al. Handb Clin Neurol. 2008;87:235-46. doi: 10.1016/S0072-9752(07)87015-1. Handb Clin Neurol. 2008. PMID: 18809029 No abstract available.
A registry for Dravet syndrome: The Italian experience.
Balestrini S, Doccini V, Giometto S, Lucenteforte E, De Masi S, Giarola E, Brambilla I, Pieroni F, Perulli M, Battaglia D, Specchio N, Ragona F, Granata T, Pellacani S, Ferrari A, Marini C, Matricardi S, Cesaroni E, Giordano L, Accorsi P, Sciruicchio V, Tinuper P, Messana T, Russo A, Pruna D, Nosadini M, De Giorgis V, Caputo D; Residras Collaboration Group; Pellegrin S, Lo Barco T, Darra F, Dalla Bernardina B, Guerrini R. Balestrini S, et al. Among authors: granata t. Epilepsia Open. 2023 Jun;8(2):517-534. doi: 10.1002/epi4.12730. Epub 2023 Mar 30. Epilepsia Open. 2023. PMID: 36938796 Free PMC article.
Inflammatory pathways of seizure disorders.
Marchi N, Granata T, Janigro D. Marchi N, et al. Among authors: granata t. Trends Neurosci. 2014 Feb;37(2):55-65. doi: 10.1016/j.tins.2013.11.002. Epub 2013 Dec 16. Trends Neurosci. 2014. PMID: 24355813 Free PMC article. Review.
A novel de novo HCN2 loss-of-function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet.
DiFrancesco JC, Ragona F, Murano C, Frosio A, Melgari D, Binda A, Calamaio S, Prevostini R, Mauri M, Canafoglia L, Castellotti B, Messina G, Gellera C, Previtali R, Veggiotti P, Milanesi R, Barbuti A, Solazzi R, Freri E, Granata T, Rivolta I. DiFrancesco JC, et al. Among authors: granata t. Epilepsia. 2023 Dec;64(12):e222-e228. doi: 10.1111/epi.17777. Epub 2023 Oct 7. Epilepsia. 2023. PMID: 37746765
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations.
Tsai MH, Ke HC, Lin WC, Nian FS, Huang CW, Cheng HY, Hsu CS, Granata T, Chang CH, Castellotti B, Lin SY, Doniselli FM, Lu CJ, Franceschetti S, Ragona F, Hou PS, Canafoglia L, Tung CY, Lee MH, Wang WJ, Tsai JW. Tsai MH, et al. Among authors: granata t. Acta Neuropathol. 2024 Jan 9;147(1):13. doi: 10.1007/s00401-023-02665-y. Acta Neuropathol. 2024. PMID: 38194050 Free PMC article.
A novel KCNC1 gain-of-function variant causing developmental and epileptic encephalopathy: "Precision medicine" approach with fluoxetine.
Ambrosino P, Ragona F, Mosca I, Vannicola C, Canafoglia L, Solazzi R, Rivolta I, Freri E, Granata T, Messina G, Castellotti B, Gellera C, Soldovieri MV, DiFrancesco JC, Taglialatela M. Ambrosino P, et al. Among authors: granata t. Epilepsia. 2023 Jul;64(7):e148-e155. doi: 10.1111/epi.17656. Epub 2023 Jun 2. Epilepsia. 2023. PMID: 37203213
198 results