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Page 1
Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes.
Kumutpongpanich T, Ogasawara M, Ozaki A, Ishiura H, Tsuji S, Minami N, Hayashi S, Noguchi S, Iida A, Nishino I; OPDM_LRP12 Study Group; Mori-Yoshimura M, Oya Y, Ono K, Shimizu T, Kawata A, Shimohama S, Toyooka K, Endo K, Toru S, Sasaki O, Isahaya K, Takahashi MP, Iwasa K, Kira JI, Yamamoto T, Kawamoto M, Hamano T, Sugie K, Eura N, Shiota T, Koide M, Sekiya K, Kishi H, Hideyama T, Kawai S, Yanagimoto S, Sato H, Arahata H, Murayama S, Saito K, Hara H, Kanda T, Yaguchi H, Imai N, Kawagashira Y, Sanada M, Obara K, Kaido M, Furuta M, Kurashige T, Hara W, Kuzume D, Yamamoto M, Tsugawa J, Kishida H, Ishizuka N, Morimoto K, Tsuji Y, Tsuneyama A, Matsuno A, Sasaki R, Tamakoshi D, Abe E, Yamada S, Uzawa A. Kumutpongpanich T, et al. Among authors: hamano t. JAMA Neurol. 2021 Jul 1;78(7):853-863. doi: 10.1001/jamaneurol.2021.1509. JAMA Neurol. 2021. PMID: 34047774 Free PMC article.
Muscle MRI in myotonic dystrophy type 1 with foot drop.
Hamano T, Kawamura Y, Mutoh T, Hirayama M, Kuriyama M. Hamano T, et al. Eur Neurol. 2010;63(3):144-8. doi: 10.1159/000280763. Epub 2010 Feb 5. Eur Neurol. 2010. PMID: 20134167 Free article.
Muscle MRI of the Upper Extremity in the Myotonic Dystrophy Type 1.
Hayashi K, Hamano T, Kawamura Y, Kimura H, Matsunaga A, Ikawa M, Yamamura O, Mutoh T, Higuchi I, Kuriyama M, Nakamoto Y. Hayashi K, et al. Among authors: hamano t. Eur Neurol. 2016;76(1-2):87-94. doi: 10.1159/000448328. Epub 2016 Jul 29. Eur Neurol. 2016. PMID: 27466802
[A case of anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase antibody-positive paraneoplastic necrotizing myopathy associated with advanced gastric cancer that responded to intravenous immunoglobulin therapy].
Yamaguchi T, Matsunaga A, Ikawa M, Shirafuji N, Nishino I, Hamano T. Yamaguchi T, et al. Among authors: hamano t. Rinsho Shinkeigaku. 2017 Mar 28;57(3):118-123. doi: 10.5692/clinicalneurol.cn-000982. Epub 2017 Feb 22. Rinsho Shinkeigaku. 2017. PMID: 28228619 Japanese.
Simultaneous measurement of the size and methylation of chromosome 4qA-D4Z4 repeats in facioscapulohumeral muscular dystrophy by long-read sequencing.
Hiramuki Y, Kure Y, Saito Y, Ogawa M, Ishikawa K, Mori-Yoshimura M, Oya Y, Takahashi Y, Kim DS, Arai N, Mori C, Matsumura T, Hamano T, Nakamura K, Ikezoe K, Hayashi S, Goto Y, Noguchi S, Nishino I. Hiramuki Y, et al. Among authors: hamano t. J Transl Med. 2022 Nov 8;20(1):517. doi: 10.1186/s12967-022-03743-7. J Transl Med. 2022. PMID: 36348371 Free PMC article.
691 results