Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Dimitri M Kullmann

Showing results (221-230 of 237) with videos related to

Pageof 24
Sort By:
Annals of Neurology|September 13, 2025
Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental StudyAdeline Ngoh, Maria Clark, Rebecca Greenaway, et al.
Journal of Neuroscience Methods|February 11, 2018
Imaging pathological activities of human brain tissue in organotypic cultureCaroline Le Duigou, Etienne Savary, Mélanie Morin-Brureau, 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.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2018
Spider toxin inhibits gating pore currents underlying periodic paralysisRoope Männikkö, Zakhar O Shenkarev, Michael G Thor, et al.
Frontiers in Pharmacology|September 27, 2019
Cell-Free Expression of Sodium Channel Domains for Pharmacology Studies. Noncanonical Spider Toxin Binding Site in the Second Voltage-Sensing Domain of Human Na<sub>v</sub>1.4 ChannelMikhail Yu Myshkin, Roope Männikkö, Olesya A Krumkacheva, et al.
BMC Biology|June 22, 2018
Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutantsGemma F Codner, Joffrey Mianné, Adam Caulder, et al.
Lancet (London, England)|April 2, 2018
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control studyRoope Männikkö, Leonie Wong, David J Tester, et al.
Epilepsia|November 1, 2022
De novo KCNA6 variants with attenuated K<sub>V</sub> 1.6 channel deactivation in patients with epilepsyVincenzo Salpietro, Valentina Galassi Deforie, Stephanie Efthymiou, et al.
Neurology|October 19, 2012
PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraineAlice R Gardiner, Kailash P Bhatia, Maria Stamelou, et al.
The Lancet. Neurology|May 17, 2024
Climate change and disorders of the nervous systemSanjay M Sisodiya, Medine I Gulcebi, Francesco Fortunato, et al.
Pageof 24

Showing results (221-230 of 237) with videos related to

Sort By:
Pageof 24
Annals of Neurology|September 13, 2025
Clinical and Molecular Genetic Characterization of Landau Kleffner Syndrome: An Observational Cohort and Experimental StudyAdeline Ngoh, Maria Clark, Rebecca Greenaway, et al.
Journal of Neuroscience Methods|February 11, 2018
Imaging pathological activities of human brain tissue in organotypic cultureCaroline Le Duigou, Etienne Savary, Mélanie Morin-Brureau, 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.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2018
Spider toxin inhibits gating pore currents underlying periodic paralysisRoope Männikkö, Zakhar O Shenkarev, Michael G Thor, et al.
Frontiers in Pharmacology|September 27, 2019
Cell-Free Expression of Sodium Channel Domains for Pharmacology Studies. Noncanonical Spider Toxin Binding Site in the Second Voltage-Sensing Domain of Human Na<sub>v</sub>1.4 ChannelMikhail Yu Myshkin, Roope Männikkö, Olesya A Krumkacheva, et al.
BMC Biology|June 22, 2018
Application of long single-stranded DNA donors in genome editing: generation and validation of mouse mutantsGemma F Codner, Joffrey Mianné, Adam Caulder, et al.
Lancet (London, England)|April 2, 2018
Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control studyRoope Männikkö, Leonie Wong, David J Tester, et al.
Epilepsia|November 1, 2022
De novo KCNA6 variants with attenuated K<sub>V</sub> 1.6 channel deactivation in patients with epilepsyVincenzo Salpietro, Valentina Galassi Deforie, Stephanie Efthymiou, et al.
Neurology|October 19, 2012
PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraineAlice R Gardiner, Kailash P Bhatia, Maria Stamelou, et al.
The Lancet. Neurology|May 17, 2024
Climate change and disorders of the nervous systemSanjay M Sisodiya, Medine I Gulcebi, Francesco Fortunato, et al.
Pageof 24