Yuka Urata

发表

Sleep Disorders in Four Patients With Myotonic Dystrophy Type 1

A. Sano, Masayuki Nakamura, T. Ishizuka, 2020, Frontiers in Neurology.

A patient with McLeod syndrome showing involvement of the central sensorimotor tracts for the legs

M. Abe, H. Matsumoto, Y. Ugawa, 2019, BMC Neurology.

Chorein interacts with α‐tubulin and histone deacetylase 6, and overexpression preserves cell viability during nutrient deprivation in human embryonic kidney 293 cells

A. Sano, Natsuki Sasaki, Masayuki Nakamura, 2016, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Novel pathogenic XK mutations in McLeod syndrome and interaction between XK protein and chorein

Y. Ugawa, T. Murakami, A. Sano, 2019, Neurology: Genetics.

Novel pathogenic VPS13A gene mutations in Japanese patients with chorea-acanthocytosis

T. Fujii, Yuji Takahashi, H. Mochizuki, 2019, Neurology: Genetics.

Mouse model of chorea-acanthocytosis exhibits male infertility caused by impaired sperm motility as a result of ultrastructural morphological abnormalities in the mitochondrial sheath in the sperm midpiece.

A. Sano, Natsuki Sasaki, Masayuki Nakamura, 2018, Biochemical and biophysical research communications.

DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

Y. Goto, S. Niwa, A. Sano, 2020, Journal of Human Genetics.

A. Sano, Masayuki Nakamura, Yuka Urata, 2023, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Correction to: DNA analysis of benign adult familial myoclonic epilepsy reveals associations between the pathogenic TTTCA repeat insertion in SAMD12 and the nonpathogenic TTTTA repeat expansion in TNRC6A

Y. Goto, S. Niwa, A. Sano, 2020, Journal of human genetics.