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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 10
2017 15
2018 15
2019 11
2020 18
2021 25
2022 15
2023 11
2024 9

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318 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.
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction.
den Hoed J, de Boer E, Voisin N, Dingemans AJM, Guex N, Wiel L, Nellaker C, Amudhavalli SM, Banka S, Bena FS, Ben-Zeev B, Bonagura VR, Bruel AL, Brunet T, Brunner HG, Chew HB, Chrast J, Cimbalistienė L, Coon H; DDD Study; Délot EC, Démurger F, Denommé-Pichon AS, Depienne C, Donnai D, Dyment DA, Elpeleg O, Faivre L, Gilissen C, Granger L, Haber B, Hachiya Y, Abedi YH, Hanebeck J, Hehir-Kwa JY, Horist B, Itai T, Jackson A, Jewell R, Jones KL, Joss S, Kashii H, Kato M, Kattentidt-Mouravieva AA, Kok F, Kotzaeridou U, Krishnamurthy V, Kučinskas V, Kuechler A, Lavillaureix A, Liu P, Manwaring L, Matsumoto N, Mazel B, McWalter K, Meiner V, Mikati MA, Miyatake S, Mizuguchi T, Moey LH, Mohammed S, Mor-Shaked H, Mountford H, Newbury-Ecob R, Odent S, Orec L, Osmond M, Palculict TB, Parker M, Petersen AK, Pfundt R, Preikšaitienė E, Radtke K, Ranza E, Rosenfeld JA, Santiago-Sim T, Schwager C, Sinnema M, Snijders Blok L, Spillmann RC, Stegmann APA, Thiffault I, Tran L, Vaknin-Dembinsky A, Vedovato-Dos-Santos JH, Schrier Vergano SA, Vilain E, Vitobello A, Wagner M, Waheeb A, Willing M, Zuccarelli B, Kini U, Newbury DF, Kleefstra T, Reymond A, Fisher SE, Vissers LELM. den Hoed J, et al. Among authors: mikati ma. Am J Hum Genet. 2021 Feb 4;108(2):346-356. doi: 10.1016/j.ajhg.2021.01.007. Epub 2021 Jan 28. Am J Hum Genet. 2021. PMID: 33513338 Free PMC article.
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.
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.
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.
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.
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.
Early Clinical Variables Associated With Refractory Convulsive Status Epilepticus in Children.
Peariso K, Arya R, Glauser T, Abend NS, Barcia Aguilar C, Amengual-Gual M, Anderson A, Appavu BL, Brenton JN, Carpenter J, Chapman KE, Clark J, Gaillard WD, Gaínza-Lein M, Goldstein J, Goodkin H, Grinspan Z, Guerriero RM, Horn PS, Huh L, Kahoud R, Kelley SA, Kossoff EH, Kapur K, Lai YC, Marquis BO, McDonough T, Mikati MA, Morgan L, Novotny E, Ostendorf AP, Payne ET, Piantino J, Riviello J, Sands T, Stafstrom CE, Tasker RC, Tchapyjnikov D, Vasquez A, Wainwright MS, Wilfong A, Williams K, Loddenkemper T; for Pediatric Status Epilepticus Research Group (pSERG). Peariso K, et al. Among authors: mikati ma. Neurology. 2023 Aug 1;101(5):e546-e557. doi: 10.1212/WNL.0000000000207472. Epub 2023 Jun 9. Neurology. 2023. PMID: 37295955 Free PMC article.
Somatic variants in diverse genes leads to a spectrum of focal cortical malformations.
Lai D, Gade M, Yang E, Koh HY, Lu J, Walley NM, Buckley AF, Sands TT, Akman CI, Mikati MA, McKhann GM, Goldman JE, Canoll P, Alexander AL, Park KL, Von Allmen GK, Rodziyevska O, Bhattacharjee MB, Lidov HGW, Vogel H, Grant GA, Porter BE, Poduri AH, Crino PB, Heinzen EL. Lai D, et al. Among authors: mikati ma. Brain. 2022 Aug 27;145(8):2704-2720. doi: 10.1093/brain/awac117. Brain. 2022. PMID: 35441233 Free PMC article.
318 results