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Muscle & Nerve|February 12, 2009
Clinical and genetic analysis of lipid storage myopathiesAya Ohkuma, Satoru Noguchi, Hideo Sugie, et al.International Journal of Molecular Sciences|November 11, 2018
A Nationwide Survey on Danon Disease in JapanKazuma Sugie, Hirofumi Komaki, Nobuyuki Eura, et al.Journal of Neuropathology and Experimental Neurology|June 28, 2005
Autophagic vacuoles with sarcolemmal features delineate Danon disease and related myopathiesKazuma Sugie, Satoru Noguchi, Yoshimichi Kozuka, et al.Neuromuscular Disorders : NMD|April 19, 2005
Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in JapanHiroshi Matsumoto, Yukiko K Hayashi, Dae-Son Kim, et al.Neuromuscular Disorders : NMD|June 26, 2009
Nemaline (actin) myopathy with myofibrillar dysgenesis and abnormal ossificationAsako Arai, Satomi Mitsuhashi, Yoshiaki Saito, et al.Neuromuscular Disorders : NMD|February 12, 2013
DNAJB6 myopathy in an Asian cohort and cytoplasmic/nuclear inclusionsTakatoshi Sato, Yukiko K Hayashi, Yasushi Oya, et al.The Journal of Clinical Investigation|September 4, 2009
Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophyYukiko K Hayashi, Chie Matsuda, Megumu Ogawa, et al.Neuromuscular Disorders : NMD|March 1, 2003
Pathological analysis of muscle hypertrophy and degeneration in muscular dystrophy in gamma-sarcoglycan-deficient miceToshikuni Sasaoka, Michihiro Imamura, Kenji Araishi, et al.The Journal of Medical Investigation : JMI|March 13, 2003
Isolation and characterization of a novel gene sfig in rat skeletal muscle up-regulated by spaceflight (STS-90)Mihoko Kano, Takako Kitano, Madoka Ikemoto, et al.Archives of Neurology|July 11, 2007
Limb-girdle muscular dystrophy due to emerin gene mutationsShigehisa Ura, Yukiko K Hayashi, Kanako Goto, et al.Pageof 17