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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
1988 4
1989 2
1990 1
1991 2
1992 3
1993 2
1994 6
1995 4
1996 4
1997 5
1998 3
1999 2
2000 2
2001 4
2002 4
2003 3
2004 3
2005 7
2006 7
2007 13
2008 14
2009 12
2010 8
2011 9
2012 8
2013 13
2014 6
2015 10
2016 9
2017 14
2018 15
2019 10
2020 16
2021 23
2022 12
2023 2

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248 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.
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.
First-line medication dosing in pediatric refractory status epilepticus.
Vasquez A, Gaínza-Lein M, Abend NS, Amengual-Gual M, Anderson A, Arya R, Brenton JN, Carpenter JL, Chapman K, Clark J, Farias-Moeller R, Gaillard WD, Glauser T, Goldstein JL, Goodkin HP, Guerriero RM, Kapur K, Lai YC, McDonough TL, Mikati MA, Morgan LA, Novotny EJ, Ostendorf AP, Payne ET, Peariso K, Piantino J, Riviello JJ, Sannagowdara K, Tasker RC, Tchapyjnikov D, Topjian A, Wainwright MS, Wilfong A, Williams K, Loddenkemper T; Pediatric Status Epilepticus Research Group (pSERG). Vasquez A, et al. Among authors: mikati ma. Neurology. 2020 Nov 10;95(19):e2683-e2696. doi: 10.1212/WNL.0000000000010828. Epub 2020 Sep 10. Neurology. 2020. PMID: 32913024 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.
Super-Refractory Status Epilepticus in Children: A Retrospective Cohort Study.
Vasquez A, Farias-Moeller R, Sánchez-Fernández I, Abend NS, Amengual-Gual M, Anderson A, Arya R, Brenton JN, Carpenter JL, Chapman K, Clark J, Gaillard WD, Glauser T, Goldstein JL, Goodkin HP, Guerriero RM, Lai YC, McDonough TL, Mikati MA, Morgan LA, Novotny EJ, Ostendorf AP, Payne ET, Peariso K, Piantino J, Riviello JJ, Sands TT, Sannagowdara K, Tasker RC, Tchapyjnikov D, Topjian A, Wainwright MS, Wilfong A, Williams K, Loddenkemper T; Pediatric Status Epilepticus Research Group (pSERG). Vasquez A, et al. Among authors: mikati ma. Pediatr Crit Care Med. 2021 Dec 1;22(12):e613-e625. doi: 10.1097/PCC.0000000000002786. Pediatr Crit Care Med. 2021. PMID: 34120133
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.
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.
248 results