Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2017 | 1 |
2022 | 2 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Common synaptic phenotypes arising from diverse mutations in the human NMDA receptor subunit GluN2A.
Commun Biol. 2022 Feb 28;5(1):174. doi: 10.1038/s42003-022-03115-3.
Commun Biol. 2022.
PMID: 35228668
Free PMC article.
Synaptic Dysfunction by Mutations in GRIN2B: Influence of Triheteromeric NMDA Receptors on Gain-of-Function and Loss-of-Function Mutant Classification.
Elmasri M, Lotti JS, Aziz W, Steele OG, Karachaliou E, Sakimura K, Hansen KB, Penn AC.
Elmasri M, et al.
Brain Sci. 2022 Jun 15;12(6):789. doi: 10.3390/brainsci12060789.
Brain Sci. 2022.
PMID: 35741674
Free PMC article.
Item in Clipboard
Decreased functional connectivity within a language subnetwork in benign epilepsy with centrotemporal spikes.
McGinnity CJ, Smith AB, Yaakub SN, Weidenbach Gerbase S, Gammerman A, Tyson AL, Bell TK, Elmasri M, Barker GJ, Richardson MP, Pal DK.
McGinnity CJ, et al. Among authors: elmasri m.
Epilepsia Open. 2017 Apr 27;2(2):214-225. doi: 10.1002/epi4.12051. eCollection 2017 Jun.
Epilepsia Open. 2017.
PMID: 29588950
Free PMC article.
Item in Clipboard
Cite
Cite