N. Yamashiro

发表

A Japanese SCA5 family with a novel three-nucleotide in-frame deletion mutation in the SPTBN2 gene: a clinical and genetic study

Y. Takiyama, Ying Wang, K. Koh, 2014, Journal of Human Genetics.

No relation between sympathetic outflow to muscles and respiratory function in amyotrophic lateral sclerosis

Y. Takiyama, K. Koh, N. Yamashiro, 2015, Journal of the Neurological Sciences.

Pre- and postganglionic vasomotor dysfunction causes distal limb coldness in multiple system atrophy

Y. Takiyama, K. Koh, N. Yamashiro, 2017, Journal of the Neurological Sciences.

[A case of hypokalemic myopathy induced by excessive drinking of a beverage containing green tea extract].

Y. Takiyama, N. Yamashiro, Megumi Fukumoto, 2013, Rinsho shinkeigaku = Clinical neurology.

Vasomotor regulation in patients with multiple system atrophy

Y. Takiyama, K. Koh, N. Yamashiro, 2017, Journal of Neural Transmission.

Exome sequencing reveals a novel missense mutation in the KIAA0196 gene in a Japanese patient with SPG8

S. Tsuji, H. Ishiura, K. Koh, 2016, Clinical Neurology and Neurosurgery.

[A case of cryptococcal ventriculitis with slowly progressive gait disturbance and memory impairment as initial symptoms].

Y. Takiyama, Michiaki Miwa, N. Yamashiro, 2015, Rinsho shinkeigaku = Clinical neurology.

[An Autopsy Case of Meningoencephalitis and Cerebral Infarction that Developed with Ramsay Hunt Syndrome and Disseminated Herpes Zoster].

Y. Takiyama, N. Yamashiro, K. Shindo, 2018, Brain and nerve = Shinkei kenkyu no shinpo.

[Cheyne-Stokes respiration appeared in an early stage of the disease in a patient with Creutzfeldt-Jakob disease].

Y. Takiyama, K. Koh, N. Yamashiro, 2013, Rinsho shinkeigaku = Clinical neurology.

Neuroimaging, genetic, and enzymatic study in a Japanese family with a GBA gross deletion.

S. Tsuji, H. Onishi, S. Morishita, 2019, Parkinsonism & related disorders.