Associated Papers
Genetics of migraine: Delineation of contemporary understanding of the genetic underpinning of migraine.
de Boer I et al.
Handbook of Clinical Neurology, 2023
Functional and Biochemical Consequences of Disease Variants in Neurotransmitter Transporters: A Special Emphasis on Folding and Trafficking Deficits.
Bhat S et al.
Pharmacology & Therapeutics, 2021
Therapeutic Potential of Sodium Channel Blockers as a Targeted Therapy Approach in KCNA1-Associated Episodic Ataxia and a Comprehensive Review of the Literature.
Lauxmann S et al.
Frontiers in Neurology, 2021
Cellular Physiology and Pathophysiology of EAAT Anion Channels.
Kovermann P et al.
Frontiers in Cellular Neuroscience, 2021
Functional consequences of SLC1A3 mutations associated with episodic ataxia 6.
Chivukula AS et al.
Human Mutation, 2020
Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants.
Sutherland HG et al.
Cells, 2020
Genetics of migraine aura: an update.
de Boer I et al.
The Journal of Headache and Pain, 2020
Impaired K+ binding to glial glutamate transporter EAAT1 in migraine.
Kovermann P et al.
Scientific Reports, 2017
Abstracts of the 2nd European Headache and Migraine Trust International Congress (EHMTIC). October 28-31, 2010. Nice, France.
Unknown Author
The Journal of Headache and Pain, 2010
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