• A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay
• Adult-onset opsoclonus-myoclonus-ataxia syndrome as a manifestation of brazilian lyme disease-like syndrome: a case report and review of literature
• Association between coenzyme Q10 and glucose transporter (GLUT1) deficiency
• Auto-immune cerebellar ataxia with anti-GAD antibodies accompanied by de novo late-onset type 1 diabetes mellitus
• Case Report: Dexmedetomidine for Intractable Clusters of Myoclonic Jerks and Paroxysmal Sympathetic Hyperactivity in Progressive Encephalomyelitis With Rigidity and Myoclonus
• Decreased cortical inhibition and yet cerebellar pathology in 'familial cortical myoclonic tremor with epilepsy'
• Epileptic encephalopathy associated with forced normalization after administration of levetiracetam
• Frequency characteristics of the semicircular canals lesion in Hunt syndrome with vertigo
• Novel missense mutation in CLN8 in late infantile neuronal ceroid lipofuscinosis: The first report of a CLN8 mutation in Japan
• NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia
• Oculomotor abnormalities in myoclonic tremor: a comparison with spinocerebellar ataxia type 6
• POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection
• Report of progressive myoclonus ataxia (PMA) in two Chinese pedigrees
• The Guillain-Mollaret triangle: a key player in motor coordination and control with implications for neurological disorders
• Unilateral facial paralysis caused by Ramsay Hunt syndrome