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Results by year

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

Year Number of Results
1959 1
1961 1
1962 2
1963 1
1964 3
1968 1
1970 1
1971 2
1973 1
1974 1
1976 2
1977 2
1978 1
1979 3
1980 4
1981 2
1982 3
1983 2
1984 2
1985 2
1986 1
1987 1
1989 4
1990 2
1991 4
1992 5
1993 7
1994 2
1995 4
1998 1
1999 1
2000 2
2001 1
2004 2
2005 1
2007 1
2009 1
2010 1
2011 2
2012 5
2013 6
2014 3
2015 8
2016 10
2017 6
2018 10
2019 10
2020 4
2021 10
2022 5
Text availability
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Article type
Publication date

Search Results

151 results
Results by year
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Page 1
Review of the Diagnosis and Treatment of Periodic Paralysis.
Statland JM, Fontaine B, Hanna MG, Johnson NE, Kissel JT, Sansone VA, Shieh PB, Tawil RN, Trivedi J, Cannon SC, Griggs RC. Statland JM, et al. Among authors: johnson ne. Muscle Nerve. 2018 Apr;57(4):522-530. doi: 10.1002/mus.26009. Epub 2017 Nov 29. Muscle Nerve. 2018. PMID: 29125635 Free PMC article. Review.
Myotonic Muscular Dystrophies.
Johnson NE. Johnson NE. Continuum (Minneap Minn). 2019 Dec;25(6):1682-1695. doi: 10.1212/CON.0000000000000793. Continuum (Minneap Minn). 2019. PMID: 31794466 Review.
Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study.
Pipis M, Feely SME, Polke JM, Skorupinska M, Perez L, Shy RR, Laura M, Morrow JM, Moroni I, Pisciotta C, Taroni F, Vujovic D, Lloyd TE, Acsadi G, Yum SW, Lewis RA, Finkel RS, Herrmann DN, Day JW, Li J, Saporta M, Sadjadi R, Walk D, Burns J, Muntoni F, Ramchandren S, Horvath R, Johnson NE, Züchner S, Pareyson D, Scherer SS, Rossor AM, Shy ME, Reilly MM; Inherited Neuropathies Consortium - Rare Disease Clinical Research Network (INC-RDCRN). Pipis M, et al. Among authors: johnson ne. Brain. 2020 Dec 1;143(12):3589-3602. doi: 10.1093/brain/awaa323. Brain. 2020. PMID: 33415332 Free PMC article.
p53 convergently activates Dux/DUX4 in embryonic stem cells and in facioscapulohumeral muscular dystrophy cell models.
Grow EJ, Weaver BD, Smith CM, Guo J, Stein P, Shadle SC, Hendrickson PG, Johnson NE, Butterfield RJ, Menafra R, Kloet SL, van der Maarel SM, Williams CJ, Cairns BR. Grow EJ, et al. Among authors: johnson ne. Nat Genet. 2021 Aug;53(8):1207-1220. doi: 10.1038/s41588-021-00893-0. Epub 2021 Jul 15. Nat Genet. 2021. PMID: 34267371 Free PMC article.
Neuromuscular Disease.
Butterfield RJ, Johnson NE. Butterfield RJ, et al. Among authors: johnson ne. J Pediatr Rehabil Med. 2016;9(1):1-2. doi: 10.3233/PRM-160354. J Pediatr Rehabil Med. 2016. PMID: 26966793 No abstract available.
Repeat-associated RNA structure and aberrant splicing.
Hale MA, Johnson NE, Berglund JA. Hale MA, et al. Among authors: johnson ne. Biochim Biophys Acta Gene Regul Mech. 2019 Nov-Dec;1862(11-12):194405. doi: 10.1016/j.bbagrm.2019.07.006. Epub 2019 Jul 16. Biochim Biophys Acta Gene Regul Mech. 2019. PMID: 31323433 Free PMC article. Review.
Myotonic dystrophy: from bench to bedside.
Johnson NE, Heatwole CR. Johnson NE, et al. Semin Neurol. 2012 Jul;32(3):246-54. doi: 10.1055/s-0032-1329202. Epub 2012 Nov 1. Semin Neurol. 2012. PMID: 23117949 Review.
151 results