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

Year Number of Results
1994 1
1997 4
1998 1
1999 1
2001 1
2002 1
2003 1
2004 2
2006 1
2007 1
2008 1
2009 1
2011 1
2012 1
2013 1
2014 1
2016 1
2017 3
2018 1
2019 2
2020 4
2021 3
2022 0
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29 results
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Page 1
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.
Hamdan FF, Myers CT, Cossette P, Lemay P, Spiegelman D, Laporte AD, Nassif C, Diallo O, Monlong J, Cadieux-Dion M, Dobrzeniecka S, Meloche C, Retterer K, Cho MT, Rosenfeld JA, Bi W, Massicotte C, Miguet M, Brunga L, Regan BM, Mo K, Tam C, Schneider A, Hollingsworth G; Deciphering Developmental Disorders Study, FitzPatrick DR, Donaldson A, Canham N, Blair E, Kerr B, Fry AE, Thomas RH, Shelagh J, Hurst JA, Brittain H, Blyth M, Lebel RR, Gerkes EH, Davis-Keppen L, Stein Q, Chung WK, Dorison SJ, Benke PJ, Fassi E, Corsten-Janssen N, Kamsteeg EJ, Mau-Them FT, Bruel AL, Verloes A, Õunap K, Wojcik MH, Albert DVF, Venkateswaran S, Ware T, Jones D, Liu YC, Mohammad SS, Bizargity P, Bacino CA, Leuzzi V, Martinelli S, Dallapiccola B, Tartaglia M, Blumkin L, Wierenga KJ, Purcarin G, O'Byrne JJ, Stockler S, Lehman A, Keren B, Nougues MC, Mignot C, Auvin S, Nava C, Hiatt SM, Bebin M, Shao Y, Scaglia F, Lalani SR, Frye RE, Jarjour IT, Jacques S, Boucher RM, Riou E, Srour M, Carmant L, Lortie A, Major P, Diadori P, Dubeau F, D'Anjou G, Bourque G, Berkovic SF, Sadleir LG, Campeau PM, Kibar Z, Lafrenière RG, Girard SL, Mercimek-Mahmutoglu S, Boelman C, Rouleau GA, Scheffer IE, Mefford HC, Andrade DM, Rossignol E, Minassian BA, Michaud JL. Hamdan FF, et al. Among authors: bebin m. Am J Hum Genet. 2017 Nov 2;101(5):664-685. doi: 10.1016/j.ajhg.2017.09.008. Am J Hum Genet. 2017. PMID: 29100083 Free PMC article.
Antiepileptogenesis and disease modification: Clinical and regulatory issues.
French JA, Bebin M, Dichter MA, Engel J Jr, Hartman AL, Jóźwiak S, Klein P, McNamara J Sr, Twyman R, Vespa P. French JA, et al. Among authors: bebin m. Epilepsia Open. 2021 Sep;6(3):483-492. doi: 10.1002/epi4.12526. Epub 2021 Jul 29. Epilepsia Open. 2021. PMID: 34270884 Free PMC article.
Pediatric partial and generalized seizures.
Bebin M. Bebin M. J Child Neurol. 2002 Jan;17 Suppl 1:S65-9. doi: 10.1177/08830738020170010901. J Child Neurol. 2002. PMID: 11918466 Review.
The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child's Best Possible Life.
Childerhose JE, Rich C, East KM, Kelley WV, Simmons S, Finnila CR, Bowling K, Amaral M, Hiatt SM, Thompson M, Gray DE, Lawlor JMJ, Myers RM, Barsh GS, Lose EJ, Bebin ME, Cooper GM, Brothers KB. Childerhose JE, et al. Among authors: bebin me. AJOB Empir Bioeth. 2021 Jul-Sep;12(3):179-189. doi: 10.1080/23294515.2021.1907475. Epub 2021 Apr 12. AJOB Empir Bioeth. 2021. PMID: 33843487
Deep learning in rare disease. Detection of tubers in tuberous sclerosis complex.
Sánchez Fernández I, Yang E, Calvachi P, Amengual-Gual M, Wu JY, Krueger D, Northrup H, Bebin ME, Sahin M, Yu KH, Peters JM; TACERN Study Group. Sánchez Fernández I, et al. Among authors: bebin me. PLoS One. 2020 Apr 29;15(4):e0232376. doi: 10.1371/journal.pone.0232376. eCollection 2020. PLoS One. 2020. PMID: 32348367 Free PMC article.
29 results