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Rinsho Shinkeigaku = Clinical Neurology|January 18, 2005
[Clinical features and molecular genetics of autosomal recessive spinocerebellar degenerations]Shoji TsujiRinsho Shinkeigaku = Clinical Neurology|May 22, 2004
[How should we establish professional education system for neurologists?]Shoji TsujiRinsho Shinkeigaku = Clinical Neurology|December 3, 2013
[Overview -- exploring molecular basis of sporadic neurologic disorders]Shoji TsujiCerebellum (London, England)|November 30, 2021
Frequency of FMR1 Premutation Alleles in Patients with Undiagnosed Cerebellar Ataxia and Multiple System Atrophy in the Japanese PopulationAsem Almansour, Hiroyuki Ishiura, Jun Mitsui, et al.Journal of the Neurological Sciences|August 29, 2021
COQ2 V393A confers high risk susceptibility for multiple system atrophy in East Asian populationKristine Joyce Porto, Makito Hirano, Jun Mitsui, et al.Neurogenetics|January 27, 2011
Posterior column ataxia with retinitis pigmentosa in a Japanese family with a novel mutation in FLVCR1Hiroyuki Ishiura, Yoko Fukuda, Jun Mitsui, et al.Journal of the Neurological Sciences|January 31, 2006
Pathology of the sympathetic nervous system corresponding to the decreased cardiac uptake in 123I-metaiodobenzylguanidine (MIBG) scintigraphy in a patient with Parkinson diseaseJun Mitsui, Yuko Saito, Toshimitsu Momose, et al.Cerebellum (London, England)|October 13, 2022
A Novel de novo KIF1A Mutation in a Patient with Ataxia, Intellectual Disability and Mild Foot DeformityYuka Hama, Hidetoshi Date, Akiko Fujimoto, et al.Internal Medicine (Tokyo, Japan)|December 10, 2019
A Novel de novo KIF1A Mutation in a Patient with Autism, Hyperactivity, Epilepsy, Sensory Disturbance, and Spastic ParaplegiaMasanori Kurihara, Hiroyuki Ishiura, Taro Bannai, et al.Pageof 53