Fig. 1From: GABAB receptor encephalitis in a patient diagnosed with amyotrophic lateral sclerosisCerebral MRI six months after symptom onset showed cortical atrophy (a), multiple, mainly periventricular white matter lesions (b), bilateral mesiotemporal atrophy (c) and cerebellar atrophy (d). The findings are not characteristic for ALS, but occur regularly in patients with GABAB receptor encephalitisBack to article page