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[Hereditary amyloidosis].
Tashima K, Uyama E, Uchino M, Ando Y. Tashima K, et al. Among authors: uyama e. Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):636-9. Ryoikibetsu Shokogun Shirizu. 1998. PMID: 9645153 Review. Japanese. No abstract available.
Mitochondrial localization of PABPN1 in oculopharyngeal muscular dystrophy.
Doki T, Yamashita S, Wei FY, Hara K, Yamamoto T, Zhang Z, Zhang X, Tawara N, Hino H, Uyama E, Kurashige T, Maruyama H, Tomizawa K, Ando Y. Doki T, et al. Among authors: uyama e. Lab Invest. 2019 Nov;99(11):1728-1740. doi: 10.1038/s41374-019-0243-8. Epub 2019 Mar 20. Lab Invest. 2019. PMID: 30894671 Free article.
Juvenile-onset parkinsonism with digenic parkin and PINK1 mutations treated with subthalamic nucleus stimulation at 45 years after disease onset.
Nakahara K, Ueda M, Yamada K, Koide T, Yoshimochi G, Funayama M, Kim JH, Yamakawa S, Mori A, Misumi Y, Uyama E, Hattori N, Ando Y. Nakahara K, et al. Among authors: uyama e. J Neurol Sci. 2014 Oct 15;345(1-2):276-7. doi: 10.1016/j.jns.2014.07.053. Epub 2014 Aug 1. J Neurol Sci. 2014. PMID: 25106695 No abstract available.
Distribution of dystrophin and dystrophin-associated protein 43DAG (beta-dystroglycan) in the central nervous system of normal controls and patients with Duchenne muscular dystrophy.
Uchino M, Hara A, Mizuno Y, Fujiki M, Nakamura T, Tokunaga M, Hirano T, Yamashita T, Uyama E, Ando Y, Mita S, Ando M. Uchino M, et al. Among authors: uyama e. Intern Med. 1996 Mar;35(3):189-94. doi: 10.2169/internalmedicine.35.189. Intern Med. 1996. PMID: 8785451 Free article.
123 results