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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 2
2012 3
2013 4
2014 4
2015 3
2018 1
2019 4
2022 0
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97 results
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Page 1
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.
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.
Treatment of Reye syndrome.
Trauner DA. Trauner DA. Ann Neurol. 1980 Jan;7(1):2-4. doi: 10.1002/ana.410070103. Ann Neurol. 1980. PMID: 6987947 Review.
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. West J Med. 1984 Aug;141(2):206-9. West J Med. 1984. PMID: 6495727 Free PMC article.
Auditory neglect in children following perinatal stroke.
Martin K, Trauner DA. Martin K, et al. Among authors: trauner da. Behav Brain Res. 2019 Feb 1;359:878-885. doi: 10.1016/j.bbr.2018.06.026. Epub 2018 Jun 25. Behav Brain Res. 2019. PMID: 29953906
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
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.
Executive function in nephropathic cystinosis.
Ballantyne AO, Spilkin AM, Trauner DA. Ballantyne AO, et al. Among authors: trauner da. Cogn Behav Neurol. 2013 Mar;26(1):14-22. doi: 10.1097/WNN.0b013e31828b9f11. Cogn Behav Neurol. 2013. PMID: 23538568 Free PMC article.
97 results