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

Year Number of Results
1984 1
1986 1
1990 2
1991 3
1992 2
1993 3
1994 3
1995 3
1996 5
1997 8
1998 2
1999 2
2000 4
2002 3
2003 4
2004 1
2005 2
2006 3
2007 5
2008 3
2009 6
2010 4
2011 5
2012 3
2013 3
2014 6
2015 1
2017 2
2018 1
2022 1
2024 0

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84 results

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Page 1
Huntington disease: natural history, biomarkers and prospects for therapeutics.
Ross CA, Aylward EH, Wild EJ, Langbehn DR, Long JD, Warner JH, Scahill RI, Leavitt BR, Stout JC, Paulsen JS, Reilmann R, Unschuld PG, Wexler A, Margolis RL, Tabrizi SJ. Ross CA, et al. Among authors: aylward eh. Nat Rev Neurol. 2014 Apr;10(4):204-16. doi: 10.1038/nrneurol.2014.24. Epub 2014 Mar 11. Nat Rev Neurol. 2014. PMID: 24614516 Free article. Review.
Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset.
McAllister B, Donaldson J, Binda CS, Powell S, Chughtai U, Edwards G, Stone J, Lobanov S, Elliston L, Schuhmacher LN, Rees E, Menzies G, Ciosi M, Maxwell A, Chao MJ, Hong EP, Lucente D, Wheeler V, Lee JM, MacDonald ME, Long JD, Aylward EH, Landwehrmeyer GB, Rosser AE; REGISTRY Investigators of the European Huntington’s disease network; Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group; Williams NM, Gusella JF, Monckton DG, Allen ND, Holmans P, Jones L, Massey TH. McAllister B, et al. Among authors: aylward eh. Nat Neurosci. 2022 Apr;25(4):446-457. doi: 10.1038/s41593-022-01033-5. Epub 2022 Apr 4. Nat Neurosci. 2022. PMID: 35379994 Free PMC article.
Converging evidence for triple word form theory in children with dyslexia.
Richards TL, Aylward EH, Field KM, Grimme AC, Raskind W, Richards AL, Nagy W, Eckert M, Leonard C, Abbott RD, Berninger VW. Richards TL, et al. Among authors: aylward eh. Dev Neuropsychol. 2006;30(1):547-89. doi: 10.1207/s15326942dn3001_3. Dev Neuropsychol. 2006. PMID: 16925475 Review.
Neurocognitive signs in prodromal Huntington disease.
Stout JC, Paulsen JS, Queller S, Solomon AC, Whitlock KB, Campbell JC, Carlozzi N, Duff K, Beglinger LJ, Langbehn DR, Johnson SA, Biglan KM, Aylward EH. Stout JC, et al. Among authors: aylward eh. Neuropsychology. 2011 Jan;25(1):1-14. doi: 10.1037/a0020937. Neuropsychology. 2011. PMID: 20919768 Free PMC article.
Genetic Modification of Huntington Disease Acts Early in the Prediagnosis Phase.
Long JD, Lee JM, Aylward EH, Gillis T, Mysore JS, Abu Elneel K, Chao MJ, Paulsen JS, MacDonald ME, Gusella JF. Long JD, et al. Among authors: aylward eh. Am J Hum Genet. 2018 Sep 6;103(3):349-357. doi: 10.1016/j.ajhg.2018.07.017. Epub 2018 Aug 16. Am J Hum Genet. 2018. PMID: 30122542 Free PMC article.
Neurochemical correlates of caudate atrophy in Huntington's disease.
Padowski JM, Weaver KE, Richards TL, Laurino MY, Samii A, Aylward EH, Conley KE. Padowski JM, et al. Among authors: aylward eh. Mov Disord. 2014 Mar;29(3):327-35. doi: 10.1002/mds.25801. Epub 2014 Jan 17. Mov Disord. 2014. PMID: 24442623 Free PMC article.
84 results