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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

86 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
CHD2 mutations in Lennox-Gastaut syndrome.
Lund C, Brodtkorb E, Øye AM, Røsby O, Selmer KK. Lund C, et al. Among authors: selmer kk. Epilepsy Behav. 2014 Apr;33:18-21. doi: 10.1016/j.yebeh.2014.02.005. Epub 2014 Mar 12. Epilepsy Behav. 2014. PMID: 24614520
Longitudinal changes of serum cytokines in patients with chronic low back pain and Modic changes.
Gjefsen E, Gervin K, Bråten LCH, Goll GL, Aass HCD, Schistad EI, Wigemyr M, Pedersen LM, Skouen JS, Vigeland MD, Selmer KK, Storheim K, Zwart JA. Gjefsen E, et al. Among authors: selmer kk. Osteoarthritis Cartilage. 2023 Apr;31(4):543-547. doi: 10.1016/j.joca.2023.01.001. Epub 2023 Jan 12. Osteoarthritis Cartilage. 2023. PMID: 36640896 Free article. Clinical Trial.
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.
Gilfillan GD, Selmer KK, Roxrud I, Smith R, Kyllerman M, Eiklid K, Kroken M, Mattingsdal M, Egeland T, Stenmark H, Sjøholm H, Server A, Samuelsson L, Christianson A, Tarpey P, Whibley A, Stratton MR, Futreal PA, Teague J, Edkins S, Gecz J, Turner G, Raymond FL, Schwartz C, Stevenson RE, Undlien DE, Strømme P. Gilfillan GD, et al. Among authors: selmer kk. Am J Hum Genet. 2008 Apr;82(4):1003-10. doi: 10.1016/j.ajhg.2008.01.013. Epub 2008 Mar 13. Am J Hum Genet. 2008. PMID: 18342287 Free PMC article.
[Dravet syndrome as a cause of epilepsy and learning disability].
Lund C, Bremer A, Lossius MI, Selmer KK, Brodtkorb E, Nakken KO. Lund C, et al. Among authors: selmer kk. Tidsskr Nor Laegeforen. 2012 Jan 10;132(1):44-7. doi: 10.4045/tidsskr.11.0539. Tidsskr Nor Laegeforen. 2012. PMID: 22240828 Free article. Review. Norwegian.
Aicardi syndrome: an epidemiologic and clinical study in Norway.
Lund C, Bjørnvold M, Tuft M, Kostov H, Røsby O, Selmer KK. Lund C, et al. Among authors: selmer kk. Pediatr Neurol. 2015 Feb;52(2):182-6.e3. doi: 10.1016/j.pediatrneurol.2014.10.022. Epub 2014 Oct 31. Pediatr Neurol. 2015. PMID: 25443581
86 results