Takeshi Nakamura

Genetic Creutzfeldt–Jakob disease‐M232R with the cooccurrence of multiple prion strains, M1 + M2C + M2T: Report of an autopsy case

A. Shinde, H. Kusaka, T. Kitamoto, 2021, Neuropathology : official journal of the Japanese Society of Neuropathology.

Syndrome of Inappropriate Antidiuretic Hormone Secretion Associated with Amyotrophic Lateral Sclerosis in a Patient Developing Carbon Dioxide Narcosis

I. Nishino, S. Yonemitsu, Tomoko S. Kato, 2017, Internal medicine.

Chédiak–Higashi syndrome presenting as a hereditary spastic paraplegia

H. Shimazaki, H. Ishiura, Y. Takiyama, 2021, Journal of Human Genetics.

Sensorineural hearing loss and hypoplastic cochlea in Axenfeld-Rieger syndrome with FOXC1 mutation.

H. Yamazaki, Y. Hiratsuka, Y. Hotta, 2020, Auris, nasus, larynx.

A case of late‐onset Chediak‐Higashi syndrome with progressive gait disturbance and cognitive dysfunction caused by novel variant in LYST gene

Y. Takiyama, K. Koh, Makio Takahashi, 2020 .

Posterior Reversible Encephalopathy Syndrome with Extensive Deep White Matter Lesions Including the Temporal Pole

N. Mori, S. Kajikawa, J. Ohira, 2016, Internal medicine.

Chédiak–Higashi syndrome presenting as a hereditary spastic paraplegia

H. Shimazaki, H. Ishiura, Y. Takiyama, 2021, Journal of human genetics.