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Dimitri M Kullmann

Showing results (231-240 of 237) with videos related to

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Cell Reports|June 1, 2017
Progressive Motor Neuron Pathology and the Role of Astrocytes in a Human Stem Cell Model of VCP-Related ALSClaire E Hall, Zhi Yao, Minee Choi, et al.
Brain : a Journal of Neurology|October 21, 2017
Clinical, pathological and functional characterization of riboflavin-responsive neuropathyAndreea Manole, Zane Jaunmuktane, Iain Hargreaves, et al.
Nature Communications|September 4, 2015
Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizuresTommy Stödberg, Amy McTague, Arnaud J Ruiz, et al.
Epilepsy & Behavior : E&B|September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approachesFelix Rosenow, Natascha van Alphen, Albert Becker, et al.
Epilepsy & Behavior : E&B|September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part II: Experimental and translational approachesSebastian Bauer, Natascha van Alphen, Albert Becker, et al.
American Journal of Human Genetics|April 2, 2019
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human NeurodevelopmentVincenzo Salpietro, Nancy T Malintan, Isabel Llano-Rivas, et al.
Nature Communications|July 14, 2019
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disordersVincenzo Salpietro, Christine L Dixon, Hui Guo, et al.
Pageof 24

Showing results (231-240 of 237) with videos related to

Sort By:
Pageof 24
You have reached the last page of results.This site can display upto 237 results.
Cell Reports|June 1, 2017
Progressive Motor Neuron Pathology and the Role of Astrocytes in a Human Stem Cell Model of VCP-Related ALSClaire E Hall, Zhi Yao, Minee Choi, et al.
Brain : a Journal of Neurology|October 21, 2017
Clinical, pathological and functional characterization of riboflavin-responsive neuropathyAndreea Manole, Zane Jaunmuktane, Iain Hargreaves, et al.
Nature Communications|September 4, 2015
Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizuresTommy Stödberg, Amy McTague, Arnaud J Ruiz, et al.
Epilepsy & Behavior : E&B|September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part I: Clinical and network analysis approachesFelix Rosenow, Natascha van Alphen, Albert Becker, et al.
Epilepsy & Behavior : E&B|September 18, 2017
Personalized translational epilepsy research - Novel approaches and future perspectives: Part II: Experimental and translational approachesSebastian Bauer, Natascha van Alphen, Albert Becker, et al.
American Journal of Human Genetics|April 2, 2019
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human NeurodevelopmentVincenzo Salpietro, Nancy T Malintan, Isabel Llano-Rivas, et al.
Nature Communications|July 14, 2019
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disordersVincenzo Salpietro, Christine L Dixon, Hui Guo, et al.
Pageof 24