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Optogenetic and potassium channel gene therapy in a rodent model of focal neocortical epilepsy. [electronic resource] by
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Glycine receptor autoantibodies disrupt inhibitory neurotransmission. [electronic resource] by
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Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy. [electronic resource] by
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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
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- Schorge, Stephanie
- Kullmann, Dimitri M
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In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2. [electronic resource] by
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188.
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N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes. [electronic resource] by
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- Beeson, David
- Lang, Bethan
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In vivo CRISPRa decreases seizures and rescues cognitive deficits in a rodent model of epilepsy. [electronic resource] by
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- Giannelli, Serena
- Lieb, Andreas
- Schorge, Stephanie
- Kullmann, Dimitri M
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Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1. [electronic resource] by
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- Bamiou, Doris-Eva
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- Sue, Carolyn M
- Giunti, Paola
- Schorge, Stephanie
- Kullmann, Dimitri M
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Olanzapine: A potent agonist at the hM4D(Gi) DREADD amenable to clinical translation of chemogenetics. [electronic resource] by
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- During, Matthew J
- Lignani, Gabriele
- Schorge, Stephanie
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Epilepsy Gene Therapy Using an Engineered Potassium Channel. [electronic resource] by
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- Hughes, Michael P
- Massaro, Giulia
- Rahim, Ahad A
- Hashemi, Kevan S
- Kullmann, Dimitri M
- Walker, Matthew C
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- Kullmann, Dimitri M
- Acevedo-Arozena, Abraham
- Wells, Sara E
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In:
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Rhombencephalitis and Myeloradiculitis Caused by a European Subtype of Tick-Borne Encephalitis Virus. [electronic resource] by
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- Monaghan, Bernadette
- Karunaratne, Kushan
- Ciccarelli, Olga
- Spillane, Jennifer
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In:
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Nanoscale-targeted patch-clamp recordings of functional presynaptic ion channels. [electronic resource] by
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- Moss, Guy W J
- Rusakov, Dmitri A
- Klenerman, David
- Kullmann, Dimitri M
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The clinical and genetic heterogeneity of paroxysmal dyskinesias. [electronic resource] by
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- Meyer, Esther
- Xiromerisiou, Georgia
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- Walker, Matthew
- Kullmann, Dimitri
- Warner, Tom
- Jarman, Paul
- Hanna, Mike
- Kurian, Manju A
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A genetically encoded fluorescent sensor for in vivo imaging of GABA. [electronic resource] by
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- Novak, Ondrej
- Podgorski, Kaspar
- Leidenheimer, Nancy J
- Rusakov, Dmitri A
- Ahrens, Misha B
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Clinical relevance of serum antibodies to extracellular N-methyl-D-aspartate receptor epitopes. [electronic resource] by
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- Jones, Joanne L
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- Lennox, Belinda
- Stamelou, Maria
- Bhatia, Kailash P
- Schott, Jonathan M
- Coles, Alasdair J
- Kullmann, Dimitri M
- Vincent, Angela
Producer: 20150817
In:
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Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2. [electronic resource] by
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- Imbrici, Paola
- Kors, Esther E
- Terwindt, Gisela M
- Eunson, Louise H
- Frants, Rune R
- Haan, Joost
- Ferrari, Michel D
- Goadsby, Peter J
- Hanna, Michael G
- van den Maagdenberg, Arn M J M
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Producer: 20090521
In:
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Mutations in Membrin/GOSR2 Reveal Stringent Secretory Pathway Demands of Dendritic Growth and Synaptic Integrity. [electronic resource] by
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- Malintan, Nancy T
- Giachello, Carlo N G
- Patel, Nian
- Houlden, Henry
- Kullmann, Dimitri M
- Baines, Richard A
- Usowicz, Maria M
- Krishnakumar, Shyam S
- Hodge, James J L
- Rothman, James E
- Jepson, James E C
Producer: 20180522
In:
Cell reports vol. 21
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