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A case of sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: long-term observation of neurological symptoms after autologous stem-cell transplantation.
Ando T, Sato T, Kurahashi S, Kawaguchi Y, Kagaya Y, Ozawa Y, Hirano S, Goto Y, Mano K, Yokoi S, Nakamura T, Murakami A, Noda S, Kimura S, Sone J, Kuru S, Sobue G, Katsuno M. Ando T, et al. Among authors: noda s. Nagoya J Med Sci. 2021 Aug;83(3):641-647. doi: 10.18999/nagjms.83.3.641. Nagoya J Med Sci. 2021. PMID: 34552296 Free PMC article.
Impaired muscle uptake of creatine in spinal and bulbar muscular atrophy.
Hijikata Y, Katsuno M, Suzuki K, Hashizume A, Araki A, Yamada S, Inagaki T, Iida M, Noda S, Nakanishi H, Banno H, Mano T, Hirakawa A, Adachi H, Watanabe H, Yamamoto M, Sobue G. Hijikata Y, et al. Among authors: noda s. Ann Clin Transl Neurol. 2016 Jun 23;3(7):537-46. doi: 10.1002/acn3.324. eCollection 2016 Jul. Ann Clin Transl Neurol. 2016. PMID: 27386502 Free PMC article.
HMGCR antibody-associated myopathy as a paraneoplastic manifestation of esophageal carcinoma.
Tsujikawa K, Hara K, Muro Y, Nakanishi H, Niwa Y, Koike M, Noda S, Riku Y, Sahashi K, Atsuta N, Ito M, Shimoyama Y, Akiyama M, Katsuno M. Tsujikawa K, et al. Among authors: noda s. Neurology. 2016 Aug 23;87(8):841-3. doi: 10.1212/WNL.0000000000003006. Epub 2016 Jul 22. Neurology. 2016. PMID: 27449065 Free PMC article. No abstract available.
Decreased Peak Expiratory Flow Associated with Muscle Fiber-Type Switching in Spinal and Bulbar Muscular Atrophy.
Yamada S, Hashizume A, Hijikata Y, Inagaki T, Suzuki K, Kondo N, Kawai K, Noda S, Nakanishi H, Banno H, Hirakawa A, Koike H, Halievski K, Jordan CL, Katsuno M, Sobue G. Yamada S, et al. Among authors: noda s. PLoS One. 2016 Dec 22;11(12):e0168846. doi: 10.1371/journal.pone.0168846. eCollection 2016. PLoS One. 2016. PMID: 28005993 Free PMC article.
Inflammatory myopathy associated with PD-1 inhibitors.
Seki M, Uruha A, Ohnuki Y, Kamada S, Noda T, Onda A, Ohira M, Isami A, Hiramatsu S, Hibino M, Nakane S, Noda S, Yutani S, Hanazono A, Yaguchi H, Takao M, Shiina T, Katsuno M, Nakahara J, Matsubara S, Nishino I, Suzuki S. Seki M, et al. Among authors: noda s, noda t. J Autoimmun. 2019 Jun;100:105-113. doi: 10.1016/j.jaut.2019.03.005. Epub 2019 Mar 10. J Autoimmun. 2019. PMID: 30862448 Clinical Trial.
Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy.
Iida M, Sahashi K, Kondo N, Nakatsuji H, Tohnai G, Tsutsumi Y, Noda S, Murakami A, Onodera K, Okada Y, Nakatochi M, Tsukagoshi Okabe Y, Shimizu S, Mizuno M, Adachi H, Okano H, Sobue G, Katsuno M. Iida M, et al. Among authors: noda s. Nat Commun. 2019 Sep 19;10(1):4262. doi: 10.1038/s41467-019-12282-7. Nat Commun. 2019. PMID: 31537808 Free PMC article.
The wide-ranging clinical and genetic features in Japanese families with valosin-containing protein proteinopathy.
Ando T, Nakamura R, Kuru S, Yokoi D, Atsuta N, Koike H, Suzuki M, Hara K, Iguchi Y, Harada Y, Yoshida Y, Hattori M, Murakami A, Noda S, Kimura S, Sone J, Nakamura T, Goto Y, Mano K, Okada H, Okuda S, Nishino I, Ogi T, Sobue G, Katsuno M. Ando T, et al. Among authors: noda s. Neurobiol Aging. 2021 Apr;100:120.e1-120.e6. doi: 10.1016/j.neurobiolaging.2020.10.028. Epub 2020 Nov 14. Neurobiol Aging. 2021. PMID: 33339634
1,333 results