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The European Journal of Neuroscience|August 10, 2002
Functional characterization of compound heterozygosity for GlyRalpha1 mutations in the startle disease hyperekplexiaRuth Rea, Marina A Tijssen, Colin Herd, et al.Journal of Neurochemistry|September 4, 2020
Recent advances in gene therapy for neurodevelopmental disorders with epilepsyThomas J Turner, Clara Zourray, Stephanie Schorge, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|September 8, 2009
Clinical neurophysiology of the episodic ataxias: insights into ion channel dysfunction in vivoSusan E Tomlinson, Michael G Hanna, Dimitri M Kullmann, et al.Science (New York, N.Y.)|March 3, 2007
Anti-Hebbian long-term potentiation in the hippocampal feedback inhibitory circuitKarri P Lamsa, Joost H Heeroma, Peter Somogyi, et al.Muscle & Nerve|January 3, 2013
Slow channel congenital myasthenic syndrome responsive to a combination of fluoxetine and salbutamolSarah Finlayson, Jennifer Spillane, Dimitri M Kullmann, et al.Progress in Biophysics and Molecular Biology|October 9, 2004
Presynaptic, extrasynaptic and axonal GABAA receptors in the CNS: where and why?Dimitri M Kullmann, Arnaud Ruiz, Dmitri M Rusakov, et al.Elife|October 29, 2019
Dendritic NMDA receptors in parvalbumin neurons enable strong and stable neuronal assembliesJonathan H Cornford, Marion S Mercier, Marco Leite, et al.Neuron|September 16, 2003
GABAA receptors at hippocampal mossy fibersArnaud Ruiz, Ruth Fabian-Fine, Ricardo Scott, et al.Trends in Neurosciences|March 16, 2010
Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signalingStephanie Schorge, Joyce van de Leemput, Andrew Singleton, et al.Science (New York, N.Y.)|November 15, 2022
On-demand cell-autonomous gene therapy for brain circuit disordersYichen Qiu, Nathanael O'Neill, Benito Maffei, et al.Pageof 19