Cerebral Infarction and Myalgia in a 75-year-old Man with Eosinophilic Granulomatosis with Polyangiitis
Ueta, Yuki, Akiba, Yuki, Yamazaki, Jun, Okubo, Yoshihiko, Taguchi, Takeshi, Terashi, Hiroo, Hayashi, Yukiko K., Aizawa, Hitoshi
Published in Internal Medicine (01.12.2020)
Published in Internal Medicine (01.12.2020)
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Toward the development of a vibrant, super‐aged society: The future of medicine and society in Japan
Iijima, Katsuya, Arai, Hidenori, Akishita, Masahiro, Endo, Tamao, Ogasawara, Kouetsu, Kashihara, Naoki, Hayashi, Yukiko K, Yumura, Wako, Yokode, Masayuki, Ouchi, Yasuyoshi
Published in Geriatrics & gerontology international (01.08.2021)
Published in Geriatrics & gerontology international (01.08.2021)
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Inflammatory myopathy with anti-signal recognition particle antibodies: case series of 100 patients
Suzuki, Shigeaki, Nishikawa, Atsuko, Kuwana, Masataka, Nishimura, Hiroaki, Watanabe, Yurika, Nakahara, Jin, Hayashi, Yukiko K, Suzuki, Norihiro, Nishino, Ichizo
Published in Orphanet journal of rare diseases (13.05.2015)
Published in Orphanet journal of rare diseases (13.05.2015)
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Deficiency of emerin contributes differently to the pathogenesis of skeletal and cardiac muscles in LmnaH222P/H222P mutant mice
Wada, Eiji, Kato, Megumi, Yamashita, Kaori, Kokuba, Hiroko, Liang, Wen-Chen, Bonne, Gisèle, Hayashi, Yukiko K
Published in PloS one (20.08.2019)
Published in PloS one (20.08.2019)
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Homozygous nonsense variant in LRIF1 associated with facioscapulohumeral muscular dystrophy
Hamanaka, Kohei, Šikrová, Darina, Mitsuhashi, Satomi, Masuda, Hiroki, Sekiguchi, Yukari, Sugiyama, Atsuhiko, Shibuya, Kazumoto, Lemmers, Richard J L F, Goossens, Remko, Ogawa, Megumu, Nagao, Koji, Obuse, Chikashi, Noguchi, Satoru, Hayashi, Yukiko K, Kuwabara, Satoshi, Balog, Judit, Nishino, Ichizo, van der Maarel, Silvère M
Published in Neurology (09.06.2020)
Published in Neurology (09.06.2020)
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Comprehensive analysis for genetic diagnosis of Dystrophinopathies in Japan
Okubo, Mariko, Goto, Kanako, Komaki, Hirofumi, Nakamura, Harumasa, Mori-Yoshimura, Madoka, Hayashi, Yukiko K, Mitsuhashi, Satomi, Noguchi, Satoru, Kimura, En, Nishino, Ichizo
Published in Orphanet journal of rare diseases (31.08.2017)
Published in Orphanet journal of rare diseases (31.08.2017)
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Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy
Hayashi, Yukiko K, Matsuda, Chie, Ogawa, Megumu, Goto, Kanako, Tominaga, Kayo, Mitsuhashi, Satomi, Park, Young-Eun, Nonaka, Ikuya, Hino-Fukuyo, Naomi, Haginoya, Kazuhiro, Sugano, Hisashi, Nishino, Ichizo
Published in The Journal of clinical investigation (01.09.2009)
Published in The Journal of clinical investigation (01.09.2009)
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Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery-Dreifuss muscular dystrophy caused by an LMNA gene mutation
Wada, Eiji, Matsumoto, Kohei, Susumu, Nao, Kato, Megumi, Hayashi, Yukiko K
Published in The journal of physiological sciences (08.11.2023)
Published in The journal of physiological sciences (08.11.2023)
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Hepatitis C virus infection in inclusion body myositis: A case-control study
Uruha, Akinori, Noguchi, Satoru, Hayashi, Yukiko K, Tsuburaya, Rie S, Yonekawa, Takahiro, Nonaka, Ikuya, Nishino, Ichizo
Published in Neurology (19.01.2016)
Published in Neurology (19.01.2016)
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A new clinicopathological entity of IgG4-related autoimmune disease
Kamisawa, Terumi, Funata, Nobuaki, Hayashi, Yukiko, Eishi, Yoshinobu, Koike, Morio, Tsuruta, Kouji, Okamoto, Atsutake, Egawa, Naoto, Nakajima, Hitoshi
Published in Journal of gastroenterology (01.10.2003)
Published in Journal of gastroenterology (01.10.2003)
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Dominant mutations in ORAI1 cause tubular aggregate myopathy with hypocalcemia via constitutive activation of store-operated Ca²⁺ channels
Endo, Yukari, Noguchi, Satoru, Hara, Yuji, Hayashi, Yukiko K, Motomura, Kazushi, Miyatake, Satoko, Murakami, Nobuyuki, Tanaka, Satsuki, Yamashita, Sumimasa, Kizu, Rika, Bamba, Masahiro, Goto, Yu-Ichi, Matsumoto, Naomichi, Nonaka, Ikuya, Nishino, Ichizo
Published in Human molecular genetics (01.02.2015)
Published in Human molecular genetics (01.02.2015)
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TMEM43 mutations in emery-dreifuss muscular dystrophy-related myopathy
Liang, Wen-Chen, Mitsuhashi, Hiroaki, Keduka, Etsuko, Nonaka, Ikuya, Noguchi, Satoru, Nishino, Ichizo, Hayashi, Yukiko K.
Published in Annals of neurology (01.06.2011)
Published in Annals of neurology (01.06.2011)
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Clinical and histological findings associated with autoantibodies detected by RNA immunoprecipitation in inflammatory myopathies
Suzuki, Shigeaki, Yonekawa, Takahiro, Kuwana, Masataka, Hayashi, Yukiko K, Okazaki, Yuka, Kawaguchi, Yasushi, Suzuki, Norihiro, Nishino, Ichizo
Published in Journal of neuroimmunology (15.09.2014)
Published in Journal of neuroimmunology (15.09.2014)
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Two endoplasmic reticulum-associated degradation (ERAD) systems for the novel variant of the mutant dysferlin: ubiquitin/proteasome ERAD(I) and autophagy/lysosome ERAD(II)
Fujita, Eriko, Kouroku, Yoriko, Isoai, Atsushi, Kumagai, Hiromichi, Misutani, Akifumi, Matsuda, Chie, Hayashi, Yukiko K., Momoi, Takashi
Published in Human molecular genetics (15.03.2007)
Published in Human molecular genetics (15.03.2007)
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A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis
MITSUHASHI, Satomi, OHKUMA, Aya, GOTO, Kanako, KOKSAL, Burcu, KALE, Gulsev, IKEDA, Kazutaka, TAGUCHI, Ryo, NOGUCHI, Satoru, HAYASHI, Yukiko K, NONAKA, Ikuya, SHER, Roger B, SUGIMOTO, Hiroyuki, TALIM, Beril, NAKAGAWA, Yasuhito, COX, Gregory A, TOPALOGLU, Haluk, NISHINO, Ichizo, KARAHASHI, Minako, KOUMURA, Tomoko, AOYAMA, Chieko, KURIHARA, Mana, QUINLIVAN, Ros, SEWRY, Caroline, MITSUHASHI, Hiroaki
Published in American journal of human genetics (10.06.2011)
Published in American journal of human genetics (10.06.2011)
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