CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation

The International Classification of Headache Disorders, 3rd edition (beta version)

Cephalalgia · 2013 · 8.2K citations · Full text

Medicine, Neurology, Psychiatry +14

A novel recurrent mutation in ATP1A3 causes CAPOS syndrome

Michelle Demos, Clara DM van Karnebeek, Colin J.D. Ross et al. · Orphanet Journal of Rare Diseases · 2014 · 192 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Alternating hemiplegia of childhood or familial hemiplegic migraine?: A novel <i>ATP1A2</i> mutation

Kathryn J. Swoboda, Emmanuel Kanavakis, Athina Xaidara et al. · Annals of Neurology · 2004 · 169 citations

Life Sciences, Genetics, Neurology +17

Phenotypes of Spinocerebellar Ataxia Type 6 and Familial Hemiplegic Migraine Caused by a Unique CACNA1A Missense Mutation in Patients From a Large Family

Isabel Alonso, José Barros, Assunção Tuna et al. · Archives of Neurology · 2003 · 86 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome.

Paola Nicolaides, RichardE. Appleton, Alan Fryer · Journal of Medical Genetics · 1996 · 63 citations · Full text

Life Sciences, Neurology, Neuroscience +15