Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Vacuolated fibers"'
Autor:
Takashi Mikata, Takayuki Momoo, Nobue K. Iwata, Yuki Hatanaka, Ran Nakashima, Kazuhiro Ito, Shoji Tsuji, Yoshio Sakiyama, Takenari Yamashita, Yusuke Miwa, Masahiro Sonoo, Yasufumi Motoyoshi, Yoshikazu Uesaka, Yasuhisa Sakurai, Shin Kwak, Yasushi Shiio, Jun Shimizu, Masato Kadoya, Kenichi Kaida, Satoko Arai, Atsuro Chiba, Tomoko Iwanami, Aya Oda, Naoki Masuda, Hiroyuki Shimada, Yuji Hosono, Kiyoharu Inoue, Sousuke Takeuchi, Kazuhiro Kurasawa, Ayumi Hida, Manami Inoue, Hideji Hashida, Tsuneyo Mimori, Ayumi Uchibori, Reika Maezawa, Shigeo Murayama, Meiko Hashimoto Maeda, Hitoshi Aizawa, Nobuyuki Yajima, Toshihiro Yoshizawa, Yoshiharu Nakae, Hidetoshi Date
Publikováno v:
Neurology. 87:299-308
Objective: We aimed to analyze the clinical and histopathologic features of cancer-associated myositis (CAM) in relation to anti–transcriptional intermediary factor 1 γ antibody (anti-TIF1-γ-Ab), a marker of cancer association. Methods: We retros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f99c967df23bd824a312ac9f90596ffe
https://doi.org/10.1212/wnl.0000000000002863
https://doi.org/10.1212/wnl.0000000000002863
Publikováno v:
Neuromuscular Disorders. 26:S114
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2f28d2b7ab310a98465a999f7346b83
https://doi.org/10.1016/j.nmd.2016.06.105
https://doi.org/10.1016/j.nmd.2016.06.105
Autor:
Hideo Sugie, Yasushi Oya, Tokiko Fukuda, Ichizo Nishino, Kazunari Monma, Rie Tsuburaya, Ikuya Nonaka, Yukiko K. Hayashi, T. Nakayama
Publikováno v:
Neuromuscular disorders : NMD. 22(5)
Diagnosis of adult-onset Pompe disease is sometimes challenging because of its clinical similarities to muscular dystrophy and the paucity of disease-specific vacuolated fibers in the skeletal muscle pathology. We describe two patients with adult-ons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e9c657c9e703073fb5b4bf0a96978b9
https://pubmed.ncbi.nlm.nih.gov/22196155
https://pubmed.ncbi.nlm.nih.gov/22196155
Autor:
Tateo Koori, Kiyoharu Inoue, Megumu Ogawa, Michio Hirano, Ichizo Nishino, Kazuma Sugie, Ikuya Nonaka, Ayaka Yamamoto
Publikováno v:
Neuromuscular disorders : NMD. 13(9)
Danon disease, primary lysosome-associated membrane protein-2 (LAMP-2) deficiency, is histologically characterized by unusual vacuoles bound by membranes with sarcolemmal features in skeletal muscle. We studied skeletal muscle specimens from a male p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8a0769df2989185acf666672d7f0380
https://pubmed.ncbi.nlm.nih.gov/14561493
https://pubmed.ncbi.nlm.nih.gov/14561493