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Dimitri M Kullmann

Showing results (201-210 of 237) with videos related to

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The Journal of Physiology|February 17, 2010
Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsySanjeev Rajakulendran, Tracey D Graves, Robyn W Labrum, et al.
Scientific Reports|November 28, 2019
Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutationMichael G Thor, Vinojini Vivekanandam, Marisol Sampedro-Castañeda, et al.
Brain : a Journal of Neurology|September 16, 2021
Translating genetic and functional data into clinical practice: a series of 223 families with myotoniaKaren Suetterlin, Emma Matthews, Richa Sud, et al.
Brain : a Journal of Neurology|February 26, 2016
In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2Susan E Tomlinson, S Veronica Tan, David Burke, et al.
Brain : a Journal of Neurology|December 15, 2023
Anti-seizure gene therapy for focal cortical dysplasiaAmanda Almacellas Barbanoj, Robert T Graham, Benito Maffei, et al.
The Lancet. Neurology|July 1, 2026
UCL Queen Square Institute of Neurology: 75 years of innovationDimitri M Kullmann, Martina F Callaghan, Olga Ciccarelli, et al.
Brain : a Journal of Neurology|June 1, 2010
N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexesSarosh R Irani, Katarzyna Bera, Patrick Waters, et al.
Brain : a Journal of Neurology|March 5, 2020
In vivo CRISPRa decreases seizures and rescues cognitive deficits in a rodent model of epilepsyGaia Colasante, Yichen Qiu, Luca Massimino, et al.
Science Advances|April 20, 2019
Olanzapine: A potent agonist at the hM4D(Gi) DREADD amenable to clinical translation of chemogeneticsMikail Weston, Teresa Kaserer, Angela Wu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 26, 2013
Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1Susan Elizabeth Tomlinson, Sanjeev Rajakulendran, Stella Veronica Tan, et al.
Pageof 24

Showing results (201-210 of 237) with videos related to

Sort By:
Pageof 24
The Journal of Physiology|February 17, 2010
Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsySanjeev Rajakulendran, Tracey D Graves, Robyn W Labrum, et al.
Scientific Reports|November 28, 2019
Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutationMichael G Thor, Vinojini Vivekanandam, Marisol Sampedro-Castañeda, et al.
Brain : a Journal of Neurology|September 16, 2021
Translating genetic and functional data into clinical practice: a series of 223 families with myotoniaKaren Suetterlin, Emma Matthews, Richa Sud, et al.
Brain : a Journal of Neurology|February 26, 2016
In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2Susan E Tomlinson, S Veronica Tan, David Burke, et al.
Brain : a Journal of Neurology|December 15, 2023
Anti-seizure gene therapy for focal cortical dysplasiaAmanda Almacellas Barbanoj, Robert T Graham, Benito Maffei, et al.
The Lancet. Neurology|July 1, 2026
UCL Queen Square Institute of Neurology: 75 years of innovationDimitri M Kullmann, Martina F Callaghan, Olga Ciccarelli, et al.
Brain : a Journal of Neurology|June 1, 2010
N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexesSarosh R Irani, Katarzyna Bera, Patrick Waters, et al.
Brain : a Journal of Neurology|March 5, 2020
In vivo CRISPRa decreases seizures and rescues cognitive deficits in a rodent model of epilepsyGaia Colasante, Yichen Qiu, Luca Massimino, et al.
Science Advances|April 20, 2019
Olanzapine: A potent agonist at the hM4D(Gi) DREADD amenable to clinical translation of chemogeneticsMikail Weston, Teresa Kaserer, Angela Wu, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 26, 2013
Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1Susan Elizabeth Tomlinson, Sanjeev Rajakulendran, Stella Veronica Tan, et al.
Pageof 24