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

Year Number of Results
1981 1
1982 3
1984 1
1985 5
1986 1
1988 4
1989 2
1990 2
1991 3
1992 4
1993 6
1994 8
1995 9
1996 5
1997 6
1998 5
1999 5
2000 5
2001 5
2002 6
2003 5
2004 4
2005 9
2006 10
2007 15
2008 17
2009 12
2010 11
2011 9
2012 8
2013 13
2014 6
2015 12
2016 11
2017 15
2018 16
2019 13
2020 18
2021 25
2022 15
2023 12
2024 6

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321 results

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Page 1
Introduction.
Mikati MA. Mikati MA. Semin Pediatr Neurol. 2016 May;23(2):95. doi: 10.1016/j.spen.2016.06.008. Epub 2016 Jun 18. Semin Pediatr Neurol. 2016. PMID: 27544465 No abstract available.
Ataxia.
Winchester S, Singh PK, Mikati MA. Winchester S, et al. Among authors: mikati ma. Handb Clin Neurol. 2013;112:1213-7. doi: 10.1016/B978-0-444-52910-7.00043-X. Handb Clin Neurol. 2013. PMID: 23622331 Review.
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias.
Helbig KL, Lauerer RJ, Bahr JC, Souza IA, Myers CT, Uysal B, Schwarz N, Gandini MA, Huang S, Keren B, Mignot C, Afenjar A, Billette de Villemeur T, Héron D, Nava C, Valence S, Buratti J, Fagerberg CR, Soerensen KP, Kibaek M, Kamsteeg EJ, Koolen DA, Gunning B, Schelhaas HJ, Kruer MC, Fox J, Bakhtiari S, Jarrar R, Padilla-Lopez S, Lindstrom K, Jin SC, Zeng X, Bilguvar K, Papavasileiou A, Xing Q, Zhu C, Boysen K, Vairo F, Lanpher BC, Klee EW, Tillema JM, Payne ET, Cousin MA, Kruisselbrink TM, Wick MJ, Baker J, Haan E, Smith N, Sadeghpour A, Davis EE, Katsanis N; Task Force for Neonatal Genomics; Corbett MA, MacLennan AH, Gecz J, Biskup S, Goldmann E, Rodan LH, Kichula E, Segal E, Jackson KE, Asamoah A, Dimmock D, McCarrier J, Botto LD, Filloux F, Tvrdik T, Cascino GD, Klingerman S, Neumann C, Wang R, Jacobsen JC, Nolan MA, Snell RG, Lehnert K, Sadleir LG, Anderlid BM, Kvarnung M, Guerrini R, Friez MJ, Lyons MJ, Leonhard J, Kringlen G, Casas K, El Achkar CM, Smith LA, Rotenberg A, Poduri A, Sanchis-Juan A, Carss KJ, Rankin J, Zeman A, Raymond FL, Blyth M, Kerr B, Ruiz K, Urquhart J, Hughes I, Banka S; Deciphering Developmental Disorders Study; Hedrich UBS, Scheffer IE, Helbig I, Zampo… See abstract for full author list ➔ Helbig KL, et al. Am J Hum Genet. 2018 Nov 1;103(5):666-678. doi: 10.1016/j.ajhg.2018.09.006. Epub 2018 Oct 18. Am J Hum Genet. 2018. PMID: 30343943 Free PMC article.
Paroxysmal Genetic Movement Disorders and Epilepsy.
de Gusmão CM, Garcia L, Mikati MA, Su S, Silveira-Moriyama L. de Gusmão CM, et al. Among authors: mikati ma. Front Neurol. 2021 Mar 23;12:648031. doi: 10.3389/fneur.2021.648031. eCollection 2021. Front Neurol. 2021. PMID: 33833732 Free PMC article. Review.
Genetic generalized epilepsies.
Gallentine WB, Mikati MA. Gallentine WB, et al. Among authors: mikati ma. J Clin Neurophysiol. 2012 Oct;29(5):408-19. doi: 10.1097/WNP.0b013e31826bd92a. J Clin Neurophysiol. 2012. PMID: 23027098 Review.
Genetics of pediatric epilepsy.
Hani AJ, Mikati HM, Mikati MA. Hani AJ, et al. Among authors: mikati ma. Pediatr Clin North Am. 2015 Jun;62(3):703-22. doi: 10.1016/j.pcl.2015.03.013. Pediatr Clin North Am. 2015. PMID: 26022171 Review.
Therapy of Lennox-Gastaut syndrome.
Tran L, Mikati MA. Tran L, et al. Among authors: mikati ma. Epilepsy Behav. 2021 Feb;115:107665. doi: 10.1016/j.yebeh.2020.107665. Epub 2020 Dec 24. Epilepsy Behav. 2021. PMID: 33358312 No abstract available.
The expanding spectrum of ATP1A3 related disease.
Fernandes C, Mikati MA. Fernandes C, et al. Among authors: mikati ma. Eur J Paediatr Neurol. 2019 May;23(3):345-346. doi: 10.1016/j.ejpn.2019.05.007. Eur J Paediatr Neurol. 2019. PMID: 31178018 No abstract available.
Novel therapies for epilepsy in the pipeline.
Mesraoua B, Deleu D, Kullmann DM, Shetty AK, Boon P, Perucca E, Mikati MA, Asadi-Pooya AA. Mesraoua B, et al. Among authors: mikati ma. Epilepsy Behav. 2019 Aug;97:282-290. doi: 10.1016/j.yebeh.2019.04.042. Epub 2019 Jul 6. Epilepsy Behav. 2019. PMID: 31284159 Review.
321 results