Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.


The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page


My NCBI Filters

Results by year

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

Year Number of Results
1975 1
1976 1
1977 1
1979 1
1983 3
1984 1
1985 1
1987 1
1988 1
1989 4
1990 3
1991 3
1992 1
1993 11
1994 4
1995 4
1996 5
1997 7
1998 11
1999 6
2000 4
2001 6
2002 5
2003 9
2004 9
2005 7
2006 6
2007 6
2008 11
2009 6
2010 9
2011 8
2012 14
2013 11
2014 11
2015 10
2016 9
2017 5
2018 10
2019 11
2020 12
2021 8
2022 8
2023 6
2024 3

Text availability

Article attribute

Article type

Publication date

Search Results

252 results

Results by year

Filters applied: . Clear all
Page 1
Artificial Tears: A Systematic Review.
Semp DA, Beeson D, Sheppard AL, Dutta D, Wolffsohn JS. Semp DA, et al. Among authors: beeson d. Clin Optom (Auckl). 2023 Jan 10;15:9-27. doi: 10.2147/OPTO.S350185. eCollection 2023. Clin Optom (Auckl). 2023. PMID: 36647552 Free PMC article. Review.
Congenital myasthenic syndromes.
Henehan L, Beeson D, Palace J. Henehan L, et al. Among authors: beeson d. Pract Neurol. 2024 May 29;24(3):185-187. doi: 10.1136/pn-2024-004098. Pract Neurol. 2024. PMID: 38631903 Review. No abstract available.
Congenital myasthenic syndromes.
Beeson D, Palace J, Vincent A. Beeson D, et al. Curr Opin Neurol. 1997 Oct;10(5):402-7. doi: 10.1097/00019052-199710000-00008. Curr Opin Neurol. 1997. PMID: 9330886 Review.
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases.
Pagnamenta AT, Camps C, Giacopuzzi E, Taylor JM, Hashim M, Calpena E, Kaisaki PJ, Hashimoto A, Yu J, Sanders E, Schwessinger R, Hughes JR, Lunter G, Dreau H, Ferla M, Lange L, Kesim Y, Ragoussis V, Vavoulis DV, Allroggen H, Ansorge O, Babbs C, Banka S, Baños-Piñero B, Beeson D, Ben-Ami T, Bennett DL, Bento C, Blair E, Brasch-Andersen C, Bull KR, Cario H, Cilliers D, Conti V, Davies EG, Dhalla F, Dacal BD, Dong Y, Dunford JE, Guerrini R, Harris AL, Hartley J, Hollander G, Javaid K, Kane M, Kelly D, Kelly D, Knight SJL, Kreins AY, Kvikstad EM, Langman CB, Lester T, Lines KE, Lord SR, Lu X, Mansour S, Manzur A, Maroofian R, Marsden B, Mason J, McGowan SJ, Mei D, Mlcochova H, Murakami Y, Németh AH, Okoli S, Ormondroyd E, Ousager LB, Palace J, Patel SY, Pentony MM, Pugh C, Rad A, Ramesh A, Riva SG, Roberts I, Roy N, Salminen O, Schilling KD, Scott C, Sen A, Smith C, Stevenson M, Thakker RV, Twigg SRF, Uhlig HH, van Wijk R, Vona B, Wall S, Wang J, Watkins H, Zak J, Schuh AH, Kini U, Wilkie AOM, Popitsch N, Taylor JC. Pagnamenta AT, et al. Among authors: beeson d. Genome Med. 2023 Nov 9;15(1):94. doi: 10.1186/s13073-023-01240-0. Genome Med. 2023. PMID: 37946251 Free PMC article.
Inherited disorders of the neuromuscular junction: an update.
Rodríguez Cruz PM, Palace J, Beeson D. Rodríguez Cruz PM, et al. Among authors: beeson d. J Neurol. 2014 Nov;261(11):2234-43. doi: 10.1007/s00415-014-7520-7. Epub 2014 Oct 11. J Neurol. 2014. PMID: 25305004 Review.
252 results