◆ 2016 ◆

• Uruha A, Noguchi N, Hayashi YK, Tsuburaya RS, Yonekawa T, Nonaka I, Nishino I．Hepatitis C virus infection in inclusion body myositis: A case-control study. Neurology 86(3):211–217., 2016
• Sugie K, Yoshizawa H, Onoue K, Nakanishi Y, Eura N, Ogawa M, Nakano T, Sakaguchi Y, Hayashi YK, Kishimoto T, Shima M, Saito Y, Nishino I, Ueno S. Early onset of cardiomyopathy and intellectual disability in a girl with Danon disease associated with a de novo novel mutation of the LAMP2 gene. Neuropathology 36(6):561–565., 2016
• Nishikawa A, Mori-Yoshimura M, Segawa K, Hayashi YK, Takahashi T, Saito Y, Nonaka I, Krahn M, Levy N, Shimizu J, Kimura E, Goto J, Yonemoto N, Aoki M, Nishino I, Oya Y, Murata M. Respiratory and cardiac function in japanese patients with dysferlinopathy. Muscle Nerve 53(3):394–401., 2016
• Liang W-C, Choua P-C, Hung C-C, Su Y-N, Kan T-M, Chen W-Z, Hayashi YK, Nishiino I, Jong Y-J.Probable high prevalence of limb-girdle muscular dystrophy type 2D in Taiwan. J Neurol Sci 362:304–308., 2016
• Kawahara G, Hayashi YK. Characterization of Zebrafish Models of Marinesco-Sjogren Syndrome. PLoS One 11:e0165563., 2016
• Ikeda K, Mori-Yoshimura M, Yamamoto T, Sonoo M, Suzuki S, Kondo Y, Nakamura H, Mitsuhashi K, Maeda MH, Shimizu J, Hayashi YK, Nishino I, Oya Y, Murata M. Chronic Myopathy Associated With Anti-Signal Recognition Particle Antibodies Can Be Misdiagnosed As Facioscapulohumeral Muscular Dystrophy. J Clin Neuromuscul Dis 17(4):197–206., 2016
• Hamanaka K, Inami I, Wada T, Mitsuhashi S, Noguchi S, Hayashi YK, Nishino I.Muscle from a 20-week-old myotubular myopathy fetus is not myotubular. Neuromuscul Disord 26(3):234–235., 2016
• Hamanaka K, Goto K, Arai M, Nagao K, Obuse C, Noguchi S, Hayashi YK, Mitsuhashi S, Nishino I. Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations. Neuromuscul Disord 26(4-5):300–308., 2016
• Furuta M, Sumi-Akamaru H, Takahashi MP, Hayashi YK, Nishino I, Mochizuki H.An elderly-onset limb girdle muscular dystrophy type 1B (LGMD1B) with pseudo-hypertrophy of paraspinal muscles. Neuromuscul Disord 26:593–597., 2016
• Matsubara S, Shimizu T, Komori T, Mori M, Minami N, Nishino I, Hasyashi YK. Nuclear inclusions mimicking the poly(A )-binding protein nuclear 1 inclusion in a case of inclusion body myopathy with Paget disease of bone and frontotemporal dementia (IBMPFD). Neuromuscul Disord 26(7):436–440., 2016
• Dastgir J, Rutkowski A, Alvarez R, Cossette SA, Yan K, Hoffmann RG, Sewry C, Hayashi YK, Goebel HH, Bonnemann C, Lawlor MW. Common Data Elements for Muscle Biopsy 44 Reporting. Arch Pathol Lab Med 140(1):51–65., 2016