Associated Papers
Shared genetics in epilepsy and migraine: A scoping review.
Sahu P et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2025
Benign paroxysmal torticollis of infancy does not lead to neurological sequelae.
Danielsson A et al.
Developmental Medicine and Child Neurology, 2018
Retrospective genotype-phenotype analysis in a 305 patient cohort referred for testing of a targeted epilepsy panel.
Hesse AN et al.
Epilepsy Research, 2018
ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of Disease.
Friedrich T et al.
Frontiers in Physiology, 2016
27445835 (PubMed )
Supplement: Table1.PDF
Sporadic Hemiplegic Migraine with ATP1A2 and Prothrombin Gene Mutations.
Aceves J et al.
Case Reports in Neurological Medicine, 2013
Familial hemiplegic migraine in pediatric patients: A genetic, clinical, and follow-up study.
Mangano GD et al.
Headache, 0
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