Zobrazeno 1 - 10 of 75 pro vyhledávání: '"Motoyoshi Yano"'
1
Akademický článek
Intravascular lymphoma masquerading as septic shock
Autor: Hiroki Kato, Shinichi Miyazaki, Kodai Yabu, Yumi Sawada, Yuki Kondo, Tadashi Aoyama, Yoshiharu Nara, Motoyoshi Yano
Publikováno v: Clinical Case Reports, Vol 10, Iss 4, Pp n/a-n/a (2022)
Abstract Intravascular lymphoma (IVL) is a rare type of extranodal lymphoma that selectively affects small blood vessels. We report a patient who presented with dyspnea and weight loss as well as refractory shock and multiple‐organ dysfunction. The
Externí odkaz: https://doaj.org/article/4c5e358a31a8430ab3b6542729bc377f
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2
Akademický článek
A Revised Classification of Primary Iron Overload Syndromes.
Autor: Yasuaki Tatsumi, Motoyoshi Yano, Shinya Wakusawa, Hiroaki Miyajima, Tetsuya Ishikawa, Shinsaku Imashuku, Atsuko Takano, Wataru Nihei, Ayako Kato, Koichi Kato, Hisao Hayashi, Kentaro Yoshioka, Kazuhiko Hayashi
Publikováno v: Journal of Clinical & Translational Hepatology; Apr2024, Vol. 12 Issue 4, p346-356, 11p
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8
A 10-year Follow-up Study of a Japanese Family with Ferroportin Disease A: Mild Iron Overload with Mild Hyperferritinemia Co-occurring with Hyperhepcidinemia May Be Benign
Autor: Akane Mizutani, Yasuaki Tatsumi, Hisao Hayashi, Motoyoshi Yano, Naohito Urawa, Yuji Kojima, Jun Araki, Yutaka Naito, Ayako Kato, Shima Hamaoka, Koichi Kato
Publikováno v: Internal Medicine
This is a 10-year follow-up study of a family with ferroportin disease A. The proband, a 59-year-old man showed no noteworthy findings with the exception of an abnormal iron level. The proband's 90-year-old father showed reduced abilities in gait and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d2cbbb43155ff89005591cc61f7635b
http://europepmc.org/articles/PMC6207810
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9
Phenotypes and Chronic Organ Damage May Be Different among Siblings with Wilson’s Disease
Autor: Shinsuke Yahata, Takakazu Nagahara, Hidemi Goto, Masatoshi Ishigami, Motoyoshi Yano, Koichi Kato, Hiroshi Sakaeda, Yasuaki Tatsumi, Ryohei Isaji, Seitetsu Yung, Kazuhiko Hayashi, Yoji Sasaki, Mari Mandai, Shinya Wakusawa, Ayako Kato, Daisaku Kuzume, Hisao Hayashi
Publikováno v: Journal of Clinical and Translational Hepatology
Background and Aims: Cloning of ATP7B provided evidence that Wilson’s disease is a hepatic copper toxicosis with a variety of extrahepatic complications. Affected siblings with the same genetic background and exposure to similar environmental facto
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8386732bede9ddd5c0f454eab6077762
http://europepmc.org/articles/PMC5411353
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