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

Year Number of Results
1944 1
1960 3
1961 5
1962 2
1963 4
1964 2
1965 6
1966 3
1967 3
1968 3
1969 3
1970 6
1971 8
1972 5
1973 4
1974 5
1975 9
1976 5
1977 3
1978 4
1979 4
1980 5
1981 7
1982 9
1983 10
1984 6
1985 6
1986 5
1987 5
1988 6
1989 9
1990 7
1991 10
1992 11
1993 5
1994 4
1995 3
1996 11
1997 13
1998 12
1999 16
2000 16
2001 12
2002 22
2003 21
2004 24
2005 16
2006 17
2007 13
2008 15
2009 23
2010 23
2011 33
2012 21
2013 24
2014 25
2015 19
2016 28
2017 26
2018 17
2019 23
2020 17
2021 23
2022 7
Text availability
Article attribute
Article type
Publication date

Search Results

672 results
Results by year
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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: frye re. 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.
Patient care standards for primary mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society.
Parikh S, Goldstein A, Karaa A, Koenig MK, Anselm I, Brunel-Guitton C, Christodoulou J, Cohen BH, Dimmock D, Enns GM, Falk MJ, Feigenbaum A, Frye RE, Ganesh J, Griesemer D, Haas R, Horvath R, Korson M, Kruer MC, Mancuso M, McCormack S, Raboisson MJ, Reimschisel T, Salvarinova R, Saneto RP, Scaglia F, Shoffner J, Stacpoole PW, Sue CM, Tarnopolsky M, Van Karnebeek C, Wolfe LA, Cunningham ZZ, Rahman S, Chinnery PF. Parikh S, et al. Among authors: frye re. Genet Med. 2017 Dec;19(12):10.1038/gim.2017.107. doi: 10.1038/gim.2017.107. Epub 2017 Jul 27. Genet Med. 2017. PMID: 28749475 Free PMC article. Review.
Folinic acid improves verbal communication in children with autism and language impairment: a randomized double-blind placebo-controlled trial.
Frye RE, Slattery J, Delhey L, Furgerson B, Strickland T, Tippett M, Sailey A, Wynne R, Rose S, Melnyk S, Jill James S, Sequeira JM, Quadros EV. Frye RE, et al. Mol Psychiatry. 2018 Feb;23(2):247-256. doi: 10.1038/mp.2016.168. Epub 2016 Oct 18. Mol Psychiatry. 2018. PMID: 27752075 Free PMC article. Clinical Trial.
Introduction.
Frye RE, Slattery J. Frye RE, et al. Microb Ecol Health Dis. 2015 May 7;26:28168. doi: 10.3402/mehd.v26.28168. eCollection 2015. Microb Ecol Health Dis. 2015. PMID: 25956239 Free PMC article. No abstract available.
Introduction to Part 1.
Frye RE. Frye RE. Semin Pediatr Neurol. 2020 Jul;34:100802. doi: 10.1016/j.spen.2020.100802. Epub 2020 Mar 7. Semin Pediatr Neurol. 2020. PMID: 32446436
Introduction to Part 2.
Frye RE. Frye RE. Semin Pediatr Neurol. 2020 Oct;35:100828. doi: 10.1016/j.spen.2020.100828. Epub 2020 Jun 22. Semin Pediatr Neurol. 2020. PMID: 32892955
672 results