Fingerprint Fingerprint is based on mining the text of the persons scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 8 Similar Profiles
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Sodium Channels Medicine & Life Sciences
Proteins Medicine & Life Sciences
Neurons Medicine & Life Sciences
Amylases Medicine & Life Sciences
Epilepsy Medicine & Life Sciences
Exons Medicine & Life Sciences

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Grants 1987 2021

Research Output 1966 2017

Aberrant sodium channel currents and hyperexcitability of medial entorhinal cortex neurons in a mouse model of SCN8A encephalopathy

Ottolini, M., Barker, B. S., Gaykema, R. P., Meisler, M. H. & Patel, M. K. 2017 In : Journal of Neuroscience. 37, 32, p. 7643-7655 13 p.

Research output: Contribution to journalArticle

Entorhinal Cortex
Sodium Channels
Seizures
Neurons
Mutation
1 Citations

Altered gene expression profile in a mouse model of SCN8A encephalopathy

Sprissler, R. S., Wagnon, J. L., Bunton-Stasyshyn, R. K., Meisler, M. H. & Hammer, M. F. Feb 1 2017 In : Experimental Neurology. 288, p. 134-141 8 p.

Research output: Contribution to journalArticle

Transcriptome
Seizures
Mutation
Voltage-Gated Sodium Channels
Gliosis
1 Citations
Neurons
Action Potentials
Mutation
Riluzole
Voltage-Gated Sodium Channels

Severe bone loss and multiple fractures in SCN8A-related epileptic encephalopathy

Rolvien, T., Butscheidt, S., Jeschke, A., Neu, A., Denecke, J., Kubisch, C., Meisler, M. H., Pueschel, K., Barvencik, F., Yorgan, T., Oheim, R., Schinke, T. & Amling, M. Oct 1 2017 In : Bone. 103, p. 136-143 8 p.

Research output: Contribution to journalArticle

Bone and Bones
Mutation
NAV1.6 Voltage-Gated Sodium Channel
Photon Absorptiometry
Osteoclasts
6 Citations

Biallelic Mutations of VAC14 in Pediatric-Onset Neurological Disease

Lenk, G. M., Szymanska, K., Debska-Vielhaber, G., Rydzanicz, M., Walczak, A., Bekiesinska-Figatowska, M., Vielhaber, S., Hallmann, K., Stawinski, P., Buehring, S., Hsu, D. A., Kunz, W. S., Meisler, M. H. & Ploski, R. Jul 7 2016 In : American Journal of Human Genetics. 99, 1, p. 188-194 7 p.

Research output: Contribution to journalArticle

Pediatrics
Mutation
Fibroblasts
Leigh Disease
Exome