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Results by year

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

Year Number of Results
1995 1
1999 2
2002 1
2007 1
2008 2
2009 1
2010 1
2011 2
2012 4
2013 3
2014 1
2015 3
2016 1
2019 1
2020 2
2022 4
2023 1
2024 0

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28 results

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Page 1
Striatal Development in Early-Onset Huntington's Disease.
Schultz JL, Epping EA, van der Plas E, Magnotta VA, Nopoulos PC. Schultz JL, et al. Among authors: epping ea. Mov Disord. 2022 Dec;37(12):2459-2460. doi: 10.1002/mds.29227. Epub 2022 Sep 29. Mov Disord. 2022. PMID: 36177602 Free PMC article. No abstract available.
Behavioral features in child and adolescent huntingtin gene-mutation carriers.
Reasoner EE, van der Plas E, Al-Kaylani HM, Langbehn DR, Conrad AL, Schultz JL, Epping EA, Magnotta VA, Nopoulos PC. Reasoner EE, et al. Among authors: epping ea. Brain Behav. 2022 Jul;12(7):e2630. doi: 10.1002/brb3.2630. Epub 2022 May 23. Brain Behav. 2022. PMID: 35604958 Free PMC article.
Abnormal development of cerebellar-striatal circuitry in Huntington disease.
Tereshchenko AV, Schultz JL, Bruss JE, Magnotta VA, Epping EA, Nopoulos PC. Tereshchenko AV, et al. Among authors: epping ea. Neurology. 2020 May 5;94(18):e1908-e1915. doi: 10.1212/WNL.0000000000009364. Epub 2020 Apr 7. Neurology. 2020. PMID: 32265233 Free PMC article.
Pax6 3' deletion results in aniridia, autism and mental retardation.
Davis LK, Meyer KJ, Rudd DS, Librant AL, Epping EA, Sheffield VC, Wassink TH. Davis LK, et al. Among authors: epping ea. Hum Genet. 2008 May;123(4):371-8. doi: 10.1007/s00439-008-0484-x. Epub 2008 Mar 6. Hum Genet. 2008. PMID: 18322702 Free PMC article. Review.
Unawareness of motor phenoconversion in Huntington disease.
McCusker EA, Gunn DG, Epping EA, Loy CT, Radford K, Griffith J, Mills JA, Long JD, Paulsen JS; PREDICT-HD Investigators of the Huntington Study Group. McCusker EA, et al. Among authors: epping ea. Neurology. 2013 Sep 24;81(13):1141-7. doi: 10.1212/WNL.0b013e3182a55f05. Epub 2013 Aug 21. Neurology. 2013. PMID: 23966256 Free PMC article.
Abnormal brain development in child and adolescent carriers of mutant huntingtin.
van der Plas E, Langbehn DR, Conrad AL, Koscik TR, Tereshchenko A, Epping EA, Magnotta VA, Nopoulos PC. van der Plas E, et al. Among authors: epping ea. Neurology. 2019 Sep 3;93(10):e1021-e1030. doi: 10.1212/WNL.0000000000008066. Epub 2019 Aug 1. Neurology. 2019. PMID: 31371571 Free PMC article.
Depression in the early stages of Huntington disease.
Epping EA, Paulsen JS. Epping EA, et al. Neurodegener Dis Manag. 2011 Oct 1;1(5):407-414. doi: 10.2217/nmt.11.45. Neurodegener Dis Manag. 2011. PMID: 22942903 Free PMC article.
28 results