Ryosuke Miyamoto

A mutation in the low voltage-gated calcium channel CACNA1G alters the physiological properties of the channel, causing spinocerebellar ataxia

Hiroyuki Morino, Yukiko Matsuda, Keiko Muguruma et al. · Molecular Brain · 2015 · 114 citations · Full text

Cerebellar ataxia with <i>SYNE1</i> mutation accompanying motor neuron disease

Yuishin Izumi, Ryosuke Miyamoto, Hiroyuki Morino et al. · Neurology · 2013 · 66 citations

Motor Control Disorders, Motor Neuron Disease, Neurological Disorder +18

Neurologic attack and dynamic perfusion abnormality in neuronal intranuclear inclusion disease

Koji Fujita, Yusuke Osaki, Ryosuke Miyamoto et al. · Neurology Clinical Practice · 2017 · 45 citations · Full text

Neurological Disorder, Brain Lesion, Dynamic Perfusion Abnormality +20

Phenotype variability and allelic heterogeneity in KMT2B-Associated disease

Toshitaka Kawarai, Ryosuke Miyamoto, Eiji Nakagawa et al. · Parkinsonism & Related Disorders · 2018 · 38 citations

Allelic Variant, Genetics, Genetic Epidemiology +2

Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient

Hiroyuki Morino, Ryosuke Miyamoto, Shizuo Ohnishi et al. · BMC Neurology · 2014 · 36 citations · Full text