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BMC Neurology|January 13, 2019
Spinocerebellar ataxia type 31 associated with REM sleep behavior disorder: a case reportKazumasa Shindo, Tohko Sato, Hiroaki Murata, et al.
Internal Medicine (Tokyo, Japan)|April 19, 2019
Clinical and Genetic Study of the First Japanese FTDP-17 Patient with a Mutation of +3 in Intron 10 in the MAPT GeneHaitian Nan, Ryusuke Takaki, Keisuke Shimozono, et al.
Heliyon|December 14, 2020
A patient with ossification of the yellow ligament and ventriculomegaly with 22q11.2 deletion syndrome undiagnosed until adulthoodYuta Ichinose, Takafumi Kurita, Akane Satake, et al.
Journal of the Peripheral Nervous System : JPNS|November 6, 2018
Novel GARS mutation presenting as autosomal dominant intermediate Charcot-Marie-Tooth diseaseHaitian Nan, Ryusuke Takaki, Takanori Hata, et al.
Internal Medicine (Tokyo, Japan)|October 19, 2018
Exome Sequencing Reveals a Novel Homozygous Frameshift Mutation in the CYP7B1 Gene in a Japanese Patient with SPG5Haitian Nan, Keisuke Shimozono, Yuta Ichinose, et al.
BMC Neurology|June 14, 2019
Pathological findings in a patient with non-dystrophic myotonia with a mutation of the SCN4A gene; a case reportTakanori Hata, Takamura Nagasaka, Kishin Koh, et al.
Neurology. Clinical Practice|May 3, 2014
Characteristic MRI findings in beta-propeller protein-associated neurodegeneration (BPAN)Yuta Ichinose, Michiaki Miwa, Akiko Onohara, et al.
Internal Medicine (Tokyo, Japan)|June 12, 2020
A Japanese SPG4 Patient with a Confirmed De Novo Mutation of the SPAST GeneHaitian Nan, Kensho Okamoto, Lihua Gao, et al.
Epilepsy & Behavior Case Reports|March 21, 2019
Non-convulsive status epilepticus associated with neuronal intranuclear inclusion disease: A case report and literature reviewKazumasa Shindo, Mai Tsuchiya, Takanori Hata, et al.
Journal of the Neurological Sciences|September 6, 2017
Pre- and postganglionic vasomotor dysfunction causes distal limb coldness in multiple system atrophyKazumasa Shindo, Mai Tsuchiya, Yuta Ichinose, et al.
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