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

Year Number of Results
1969 1
1971 1
1972 1
1973 1
1975 2
1976 1
1977 1
1978 3
1979 1
1980 2
1981 2
1982 4
1983 2
1984 2
1985 6
1986 3
1987 2
1988 2
1989 1
1990 1
1991 3
1993 3
1994 2
1996 4
1997 2
1999 1
2000 3
2001 6
2002 2
2003 1
2004 1
2005 3
2007 6
2008 1
2009 3
2010 3
2012 4
2013 5
2014 4
2015 4
2016 3
2017 2
2018 1
2019 4
2022 1
2025 0

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105 results

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Page 1
Editorial: Neurodevelopmental disabilities.
Trauner DA. Trauner DA. Curr Opin Neurol. 2019 Aug;32(4):610. doi: 10.1097/WCO.0000000000000720. Curr Opin Neurol. 2019. PMID: 31232715 No abstract available.
Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy.
Glauser TA, Cnaan A, Shinnar S, Hirtz DG, Dlugos D, Masur D, Clark PO, Capparelli EV, Adamson PC; Childhood Absence Epilepsy Study Group. Glauser TA, et al. N Engl J Med. 2010 Mar 4;362(9):790-9. doi: 10.1056/NEJMoa0902014. N Engl J Med. 2010. PMID: 20200383 Free PMC article. Clinical Trial.
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy.
O'Donnell-Luria AH, Pais LS, Faundes V, Wood JC, Sveden A, Luria V, Abou Jamra R, Accogli A, Amburgey K, Anderlid BM, Azzarello-Burri S, Basinger AA, Bianchini C, Bird LM, Buchert R, Carre W, Ceulemans S, Charles P, Cox H, Culliton L, Currò A; Deciphering Developmental Disorders (DDD) Study; Demurger F, Dowling JJ, Duban-Bedu B, Dubourg C, Eiset SE, Escobar LF, Ferrarini A, Haack TB, Hashim M, Heide S, Helbig KL, Helbig I, Heredia R, Héron D, Isidor B, Jonasson AR, Joset P, Keren B, Kok F, Kroes HY, Lavillaureix A, Lu X, Maas SM, Maegawa GHB, Marcelis CLM, Mark PR, Masruha MR, McLaughlin HM, McWalter K, Melchinger EU, Mercimek-Andrews S, Nava C, Pendziwiat M, Person R, Ramelli GP, Ramos LLP, Rauch A, Reavey C, Renieri A, Rieß A, Sanchez-Valle A, Sattar S, Saunders C, Schwarz N, Smol T, Srour M, Steindl K, Syrbe S, Taylor JC, Telegrafi A, Thiffault I, Trauner DA, van der Linden H Jr, van Koningsbruggen S, Villard L, Vogel I, Vogt J, Weber YG, Wentzensen IM, Widjaja E, Zak J, Baxter S, Banka S, Rodan LH. O'Donnell-Luria AH, et al. Among authors: trauner da. Am J Hum Genet. 2019 Jun 6;104(6):1210-1222. doi: 10.1016/j.ajhg.2019.03.021. Epub 2019 May 9. Am J Hum Genet. 2019. PMID: 31079897 Free PMC article.
Reye's syndrome.
Trauner DA. Trauner DA. West J Med. 1984 Aug;141(2):206-9. West J Med. 1984. PMID: 6495727 Free PMC article.
Big strokes for little folks.
Trauner DA, Lo W. Trauner DA, et al. Neurology. 2014 Mar 4;82(9):742-3. doi: 10.1212/WNL.0000000000000174. Epub 2014 Jan 31. Neurology. 2014. PMID: 24489127 No abstract available.
Reye's syndrome.
Trauner DA. Trauner DA. Curr Probl Pediatr. 1982 May;12(7):1-31. doi: 10.1016/0045-9380(82)90041-x. Curr Probl Pediatr. 1982. PMID: 7094621 No abstract available.
First NIH/Office of Rare Diseases Conference on Cystinosis: past, present, and future.
Kleta R, Kaskel F, Dohil R, Goodyer P, Guay-Woodford LM, Harms E, Ingelfinger JR, Koch VH, Langman CB, Leonard MB, Mannon RB, Sarwal M, Schneider JA, Skovby F, Sonies BC, Thoene JG, Trauner DA, Gahl WA; NIH Office of Rare Diseases. Kleta R, et al. Among authors: trauner da. Pediatr Nephrol. 2005 Apr;20(4):452-4. doi: 10.1007/s00467-004-1777-5. Epub 2005 Jan 27. Pediatr Nephrol. 2005. PMID: 15747161 Review. No abstract available.
Visual and verbal learning and memory in cystinosis.
Frankel AM, Trauner DA. Frankel AM, et al. Among authors: trauner da. Brain Cogn. 2019 Oct;135:103578. doi: 10.1016/j.bandc.2019.103578. Epub 2019 Jun 21. Brain Cogn. 2019. PMID: 31233961
Clock drawing in children with perinatal stroke.
Yousefian O, Ballantyne AO, Doo A, Trauner DA. Yousefian O, et al. Among authors: trauner da. Pediatr Neurol. 2015 Jun;52(6):592-8. doi: 10.1016/j.pediatrneurol.2014.07.036. Epub 2015 Jan 31. Pediatr Neurol. 2015. PMID: 26002051 Free PMC article.
105 results