R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update
The Journal of Headache and Pain, 05/01/2012
Di Cristofori A et al. – The heterogeneous spectrum of CACNA1A gene mutations probably causes sporadic hemiplegic migraine (SHM) to be misdiagnosed. Given the therapeutic opportunities, SHM/FHM1 should be considered in differential diagnosis of patients with cerebellar ataxia and migraine with aura.



