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Synapsin- and actin-dependent frequency enhancement in mouse hippocampal mossy fiber synapses. [electronic resource] by
- Owe, Simen G
- Jensen, Vidar
- Evergren, Emma
- Ruiz, Arnaud
- Shupliakov, Oleg
- Kullmann, Dimitri M
- Storm-Mathisen, Jon
- Walaas, S Ivar
- Hvalby, Øivind
- Bergersen, Linda H
Producer: 20091217
In:
Cerebral cortex (New York, N.Y. : 1991) vol. 19
Availability: No items available.
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176.
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Anti-N-methyl-D-aspartate receptor antibodies: a potentially treatable cause of encephalitis in the intensive care unit. [electronic resource] by
- Davies, Gerard
- Irani, Sarosh R
- Coltart, Cordelia
- Ingle, Gordon
- Amin, Yogen
- Taylor, Christopher
- Radcliffe, Jeremy
- Hirsch, Nicholas P
- Howard, Robin S
- Vincent, Angela
- Kullmann, Dimitri M
Producer: 20100222
In:
Critical care medicine vol. 38
Availability: No items available.
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177.
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Optogenetic and potassium channel gene therapy in a rodent model of focal neocortical epilepsy. [electronic resource] by
- Wykes, Robert C
- Heeroma, Joost H
- Mantoan, Laura
- Zheng, Kaiyu
- MacDonald, Douglas C
- Deisseroth, Karl
- Hashemi, Kevan S
- Walker, Matthew C
- Schorge, Stephanie
- Kullmann, Dimitri M
Producer: 20130619
In:
Science translational medicine vol. 4
Availability: No items available.
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178.
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Glycine receptor autoantibodies disrupt inhibitory neurotransmission. [electronic resource] by
- Crisp, Sarah J
- Dixon, Christine L
- Jacobson, Leslie
- Chabrol, Elodie
- Irani, Sarosh R
- Leite, M Isabel
- Leschziner, Guy
- Slaght, Sean J
- Vincent, Angela
- Kullmann, Dimitri M
Producer: 20200526
In:
Brain : a journal of neurology vol. 142
Availability: No items available.
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179.
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Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy. [electronic resource] by
- Rajakulendran, Sanjeev
- Graves, Tracey D
- Labrum, Robyn W
- Kotzadimitriou, Dimitrios
- Eunson, Louise
- Davis, Mary B
- Davies, Rosalyn
- Wood, Nicholas W
- Kullmann, Dimitri M
- Hanna, Michael G
- Schorge, Stephanie
Producer: 20100827
In:
The Journal of physiology vol. 588
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180.
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Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation. [electronic resource] by
- Thor, Michael G
- Vivekanandam, Vinojini
- Sampedro-Castañeda, Marisol
- Tan, S Veronica
- Suetterlin, Karen
- Sud, Richa
- Durran, Siobhan
- Schorge, Stephanie
- Kullmann, Dimitri M
- Hanna, Michael G
- Matthews, Emma
- Männikkö, Roope
Producer: 20201109
In:
Scientific reports vol. 9
Availability: No items available.
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