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.

Https

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

Filters

My Custom Filters

Results by year

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

Year Number of Results
1989 2
1990 2
1991 1
1992 3
1993 1
1994 2
1995 5
1996 2
1997 4
1998 2
1999 1
2000 2
2002 3
2003 1
2004 1
2007 1
2008 1
2009 1
2010 2
2012 3
2013 1
2016 2
2017 7
2018 6
2019 8
2020 10
2021 2
2022 4
2023 4
2024 5
2025 3

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

81 results

Results by year

Filters applied: . Clear all
Page 1
Detailed Analysis of ITPR1 Missense Variants Guides Diagnostics and Therapeutic Design.
Tolonen JP, Parolin Schnekenberg R, McGowan S, Sims D, McEntagart M, Elmslie F, Shears D, Stewart H, Tofaris GK, Dabir T, Morrison PJ, Johnson D, Hadjivassiliou M, Ellard S, Shaw-Smith C, Znaczko A, Dixit A, Suri M, Sarkar A, Harrison RE, Jones G, Houlden H, Ceravolo G, Jarvis J, Williams J, Shanks ME, Clouston P, Rankin J, Blumkin L, Lerman-Sagie T, Ponger P, Raskin S, Granath K, Uusimaa J, Conti H, McCann E, Joss S, Blakes AJM, Metcalfe K, Kingston H, Bertoli M, Kneen R, Lynch SA, Martínez Albaladejo I, Moore AP, Jones WD; Genomics England Research Consortium; Becker EBE, Németh AH. Tolonen JP, et al. Among authors: clouston p. Mov Disord. 2024 Jan;39(1):141-151. doi: 10.1002/mds.29651. Epub 2023 Nov 14. Mov Disord. 2024. PMID: 37964426 Free PMC article.
Radiation-induced 'Meige syndrome'.
Jankelowitz SK, Clouston PD. Jankelowitz SK, et al. Among authors: clouston pd. Mov Disord. 2000 Nov;15(6):1287-8. doi: 10.1002/1531-8257(200011)15:6<1287::aid-mds1045>3.0.co;2-p. Mov Disord. 2000. PMID: 11104230 No abstract available.
Paraneoplastic syndromes.
Dalmau J, Clouston PD. Dalmau J, et al. Among authors: clouston pd. Neurology. 1992 Jul;42(7):1429. doi: 10.1212/wnl.42.7.1429. Neurology. 1992. PMID: 1620362 No abstract available.
Novel non-contiguous exon duplication in choroideremia.
Edwards TL, Williams J, Patrício MI, Simunovic MP, Shanks M, Clouston P, MacLaren RE. Edwards TL, et al. Among authors: clouston p. Clin Genet. 2018 Jan;93(1):144-148. doi: 10.1111/cge.13021. Epub 2017 Apr 19. Clin Genet. 2018. PMID: 28369842
MERTK missense variants in three patients with retinitis pigmentosa.
Poli FE, Yusuf IH, Clouston P, Shanks M, Whitfield J, Charbel Issa P, MacLaren RE. Poli FE, et al. Among authors: clouston p. Ophthalmic Genet. 2023 Feb;44(1):74-82. doi: 10.1080/13816810.2022.2113541. Epub 2022 Aug 29. Ophthalmic Genet. 2023. PMID: 36036427 Free PMC article.
CNS demyelination and quadrivalent HPV vaccination.
Sutton I, Lahoria R, Tan I, Clouston P, Barnett M. Sutton I, et al. Among authors: clouston p. Mult Scler. 2009 Jan;15(1):116-9. doi: 10.1177/1352458508096868. Epub 2008 Sep 19. Mult Scler. 2009. PMID: 18805844
Fragile XE: an important differential diagnosis.
Krishnan V, Clouston P, Crocker M, Macpherson J, Heydon F, Stewart H. Krishnan V, et al. Among authors: clouston p. BMJ Case Rep. 2010;2010:bcr06.2009.1964. doi: 10.1136/bcr.06.2009.1964. Epub 2010 Mar 23. BMJ Case Rep. 2010. PMID: 22442650 Free PMC article.
Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher Genes.
Feenstra HM, Al-Khuzaei S, Shah M, Broadgate S, Shanks M, Kamath A, Yu J, Jolly JK, MacLaren RE, Clouston P, Halford S, Downes SM. Feenstra HM, et al. Among authors: clouston p. Genes (Basel). 2022 Aug 10;13(8):1423. doi: 10.3390/genes13081423. Genes (Basel). 2022. PMID: 36011334 Free PMC article.
81 results