Shinichi Magara

A Study of Rolandic Discharges Found in Disabled Children

S. Yamazaki, Rie Izumi, Shinichi Magara, 2008 .

High prevalence of genetic alterations in early-onset epileptic encephalopathies associated with infantile movement disorders

H. Shiraishi, N. Matsumoto, Mitsuhiro Kato, 2016, Brain and Development.

The association of epileptic focus estimated by magnetoencephalography with cognitive function in non-lesional epilepsy with continuous spikes and waves during slow wave sleep (ECSWS) children

J. Tohyama, M. Yoshino, A. Saitoh, 2019, Brain and Development.

Two Cases of Pseudohypoparathyroidism Type Ia in Duozygotic Twins with Different Phenotypes

M. Uchiyama, Y. Shimomura, T. Kikuchi, 2005, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement

T. Tsunoda, T. Morio, H. Shiraishi, 2017, Scientific Reports.

Rub epilepsy in an infant with Turner syndrome

J. Tohyama, Yu Kobayashi, Noriyuki Akasaka, 2015, Brain and Development.

Polymicrogyria with calcification in Pallister-Killian syndrome detected by microarray analysis

Mitsuhiro Kato, J. Tohyama, Toshiyuki Yamamoto, 2020, Brain and Development.

Recurrence rates and risk factors for seizure recurrence following antiseizure medication withdrawal in adolescent patients with genetic generalized epilepsy

J. Tohyama, M. Fukuda, Yu Kobayashi, 2022, Epilepsia open.

Infantile epileptic encephalopathy with a hyperkinetic movement disorder and hand stereotypies associated with a novel SCN1A mutation.

N. Matsumoto, J. Tohyama, H. Saitsu, 2014, Epileptic disorders : international epilepsy journal with videotape.

Megalencephaly, polymicrogyria and ribbon-like band heterotopia: A new cortical malformation

N. Matsumoto, Mitsuhiro Kato, J. Tohyama, 2016, Brain and Development.

De novo variants in CAMK2A and CAMK2B cause neurodevelopmental disorders

K. Yokochi, H. Mutoh, T. Shiihara, 2018, Annals of clinical and translational neurology.

Severe leukoencephalopathy with cortical involvement and peripheral neuropathy due to FOLR1 deficiency

T. Akiyama, N. Matsumoto, J. Tohyama, 2017, Brain and Development.

Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement

T. Tsunoda, T. Morio, H. Shiraishi, 2017, Scientific Reports.

The association of epileptic focus estimated by magnetoencephalography with cognitive function in non-lesional epilepsy with continuous spikes and waves during slow wave sleep (ECSWS) children

J. Tohyama, M. Yoshino, A. Saitoh, 2019, Brain and Development.