Yasushi Oya

Affiliations: 
Neurology Musashi Hospital, Kawasaki-shi, Kanagawa-ken, Japan 
Google:
"Yasushi Oya"
Bio:

MUSASHI HOSPITAL
NEUROLOGY DEPT NCNPM
4-1-1 IGAWAHIGASHI-CHO
KODAIRA CITY
TOKYO, 187 8551
Japan

Mean distance: 17.82 (cluster 32)
 
SNBCP
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Sano T, Kawazoe T, Shioya A, et al. (2022) Unique Lewy pathology in myotonic dystrophy type 1. Neuropathology : Official Journal of the Japanese Society of Neuropathology. 42: 104-116
Kumutpongpanich T, Ogasawara M, Ozaki A, et al. (2021) Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes. Jama Neurology
Mori-Yoshimura M, Oya Y, Komaki H, et al. (2020) Respiratory Dysfunction in Becker Muscular Dystrophy Patients: A Case Series and Autopsy Report. Journal of Neuromuscular Diseases
Kawazoe T, Uruha A, Mori-Yoshimura M, et al. (2020) A 67-Year-Old Man with Leg Weakness and Hypertrophic Cardiomyopathy. Brain Pathology (Zurich, Switzerland). 30: 427-428
Miyazaki M, Mori-Yoshimura M, Yamamoto T, et al. (2019) Chronic sarcoid myopathy mimicking sporadic inclusion body myositis. Clinical Neurology and Neurosurgery. 182: 84-86
Isobe T, Mori-Yoshimura M, Oya Y, et al. (2017) A case of chronic sarcoid myopathy with Basedow's disease and Sjogren's syndrome: A case series of sarcoid myopathy. Rinsho Shinkeigaku = Clinical Neurology
Nishikawa A, Mori-Yoshimura M, Segawa K, et al. (2015) Respiratory and cardiac function in Japanese patients with dysferlinopathy. Muscle & Nerve
Oya Y, Proia RL, Norflus F, et al. (2000) Distribution of enzyme-bearing cells in GM2 gangliosidosis mice: regionally specific pattern of cellular infiltration following bone marrow transplantation. Acta Neuropathologica. 99: 161-8
Ezoe T, Vanier MT, Oya Y, et al. (2000) Twitcher mice with only a single active galactosylceramide synthase gene exhibit clearly detectable but therapeutically minor phenotypic improvements. Journal of Neuroscience Research. 59: 179-87
Ezoe T, Vanier MT, Oya Y, et al. (2000) Biochemistry and neuropathology of mice doubly deficient in synthesis and degradation of galactosylceramide. Journal of Neuroscience Research. 59: 170-8
See more...