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
Search Results
3 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.
Nat Genet. 2013 Sep;45(9):1067-72. doi: 10.1038/ng.2728. Epub 2013 Aug 11.
Nat Genet. 2013.
PMID: 23933819
Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region.
Reutlinger C, Helbig I, Gawelczyk B, Subero JI, Tönnies H, Muhle H, Finsterwalder K, Vermeer S, Pfundt R, Sperner J, Stefanova I, Gillessen-Kaesbach G, von Spiczak S, van Baalen A, Boor R, Siebert R, Stephani U, Caliebe A.
Reutlinger C, et al. Among authors: finsterwalder k.
Epilepsia. 2010 Sep;51(9):1870-3. doi: 10.1111/j.1528-1167.2010.02555.x.
Epilepsia. 2010.
PMID: 20384727
Free article.
Item in Clipboard
Comprehensive analysis of candidate genes for photosensitivity using a complementary bioinformatic and experimental approach.
von Spiczak S, Finsterwalder K, Muhle H, Franke A, Schilhabel M, Stephani U, Helbig I.
von Spiczak S, et al. Among authors: finsterwalder k.
Epilepsia. 2011 Oct;52(10):e143-7. doi: 10.1111/j.1528-1167.2011.03197.x. Epub 2011 Aug 29.
Epilepsia. 2011.
PMID: 21883175
Free article.
Item in Clipboard
Cite
Cite