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

Year Number of Results
2009 3
2010 15
2011 10
2012 10
2013 12
2014 7
2015 9
2016 9
2017 10
2018 2
2019 5
2023 1
2024 0

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80 results

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Page 1
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders.
Salpietro V, Dixon CL, Guo H, Bello OD, Vandrovcova J, Efthymiou S, Maroofian R, Heimer G, Burglen L, Valence S, Torti E, Hacke M, Rankin J, Tariq H, Colin E, Procaccio V, Striano P, Mankad K, Lieb A, Chen S, Pisani L, Bettencourt C, Männikkö R, Manole A, Brusco A, Grosso E, Ferrero GB, Armstrong-Moron J, Gueden S, Bar-Yosef O, Tzadok M, Monaghan KG, Santiago-Sim T, Person RE, Cho MT, Willaert R, Yoo Y, Chae JH, Quan Y, Wu H, Wang T, Bernier RA, Xia K, Blesson A, Jain M, Motazacker MM, Jaeger B, Schneider AL, Boysen K, Muir AM, Myers CT, Gavrilova RH, Gunderson L, Schultz-Rogers L, Klee EW, Dyment D, Osmond M, Parellada M, Llorente C, Gonzalez-Peñas J, Carracedo A, Van Haeringen A, Ruivenkamp C, Nava C, Heron D, Nardello R, Iacomino M, Minetti C, Skabar A, Fabretto A; SYNAPS Study Group; Raspall-Chaure M, Chez M, Tsai A, Fassi E, Shinawi M, Constantino JN, De Zorzi R, Fortuna S, Kok F, Keren B, Bonneau D, Choi M, Benzeev B, Zara F, Mefford HC, Scheffer IE, Clayton-Smith J, Macaya A, Rothman JE, Eichler EE, Kullmann DM, Houlden H. Salpietro V, et al. Nat Commun. 2019 Jul 12;10(1):3094. doi: 10.1038/s41467-019-10910-w. Nat Commun. 2019. PMID: 31300657 Free PMC article.
Autoimmune synaptopathies.
Crisp SJ, Kullmann DM, Vincent A. Crisp SJ, et al. Nat Rev Neurosci. 2016 Feb;17(2):103-17. doi: 10.1038/nrn.2015.27. Nat Rev Neurosci. 2016. PMID: 26806629 Review.
Neurological channelopathies.
Kullmann DM. Kullmann DM. Annu Rev Neurosci. 2010;33:151-72. doi: 10.1146/annurev-neuro-060909-153122. Annu Rev Neurosci. 2010. PMID: 20331364 Review.
Interneurons go plastic.
Kullmann DM, Lamsa KP. Kullmann DM, et al. Neuropharmacology. 2011 Apr;60(5):711. doi: 10.1016/j.neuropharm.2011.02.001. Epub 2011 Feb 4. Neuropharmacology. 2011. PMID: 21296094 No abstract available.
Optogenetic approaches to treat epilepsy.
Wykes RC, Kullmann DM, Pavlov I, Magloire V. Wykes RC, et al. J Neurosci Methods. 2016 Feb 15;260:215-20. doi: 10.1016/j.jneumeth.2015.06.004. Epub 2015 Jun 10. J Neurosci Methods. 2016. PMID: 26072246 Review.
Myasthenia gravis.
Spillane J, Higham E, Kullmann DM. Spillane J, et al. BMJ. 2012 Dec 21;345:e8497. doi: 10.1136/bmj.e8497. BMJ. 2012. PMID: 23261848 Review. No abstract available.
The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Gardiner AR, Jaffer F, Dale RC, Labrum R, Erro R, Meyer E, Xiromerisiou G, Stamelou M, Walker M, Kullmann D, Warner T, Jarman P, Hanna M, Kurian MA, Bhatia KP, Houlden H. Gardiner AR, et al. Brain. 2015 Dec;138(Pt 12):3567-80. doi: 10.1093/brain/awv310. Epub 2015 Nov 23. Brain. 2015. PMID: 26598494 Free PMC article. Review.
Interneuron networks in the hippocampus.
Kullmann DM. Kullmann DM. Curr Opin Neurobiol. 2011 Oct;21(5):709-16. doi: 10.1016/j.conb.2011.05.006. Epub 2011 Jun 1. Curr Opin Neurobiol. 2011. PMID: 21636266 Review.
Gene therapy in status epilepticus.
Walker MC, Schorge S, Kullmann DM, Wykes RC, Heeroma JH, Mantoan L. Walker MC, et al. Epilepsia. 2013 Sep;54 Suppl 6:43-5. doi: 10.1111/epi.12275. Epilepsia. 2013. PMID: 24001071 Free article. Review.
Myasthenia and related disorders of the neuromuscular junction.
Spillane J, Beeson DJ, Kullmann DM. Spillane J, et al. J Neurol Neurosurg Psychiatry. 2010 Aug;81(8):850-7. doi: 10.1136/jnnp.2008.169367. Epub 2010 Jun 14. J Neurol Neurosurg Psychiatry. 2010. PMID: 20547629 Review.
80 results