Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Yukio Kakuta"'
Autor:
Rei Hirose, Yuya Tsurutani, Chiho Sugisawa, Kosuke Inoue, Sachiko Suematsu, Maki Nagata, Naoki Hasegawa, Yukio Kakuta, Masato Yonamine, Kazuhiro Takekoshi, Noriko Kimura, Jun Saito, Tetsuo Nishikawa
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-8 (2021)
Abstract Background Pheochromocytoma and paraganglioma caused by succinate dehydrogenase gene mutations is called hereditary pheochromocytoma/paraganglioma syndrome. In particular, succinate dehydrogenase subunit B mutations are important because the
Externí odkaz:
https://doaj.org/article/b88ab9f5b455418e9d574877194a7475
Autor:
Haremaru Kubo, Yuya Tsurutani, Kosuke Inoue, Kazuki Watanabe, Yuto Yamazaki, Takashi Sunouchi, Yoshitomo Hoshino, Rei Hirose, Sho Katsuragawa, Hiromitsu Tannai, Yukiko Shibahara, Yukio Kakuta, Seishi Matsui, Jun Saito, Masao Omura, Hironobu Sasano, Tetsuo Nishikawa
Publikováno v:
PLoS ONE, Vol 17, Iss 4, p e0267732 (2022)
Primary aldosteronism (PA) usually accompanies suppressed plasma renin activity (PRA) through a negative feedback mechanism. While some cases of PA with unsuppressed PRA were reported, there have been no studies about the characteristics of PA with u
Externí odkaz:
https://doaj.org/article/cb6b2541ded04138b995959c602fca4b
Publikováno v:
Respirology Case Reports, Vol 8, Iss 6, Pp n/a-n/a (2020)
Abstract We describe the case of a 29‐year‐old female non‐smoker who was treated with steroid therapy for a subacute exacerbation of multisystem Langerhans cell histiocytosis (MS‐LCH) with worsening lung, skin, and oral mucosal lesions. The p
Externí odkaz:
https://doaj.org/article/0bfb994b01a5493a85d5c836cf9fd2d5
Autor:
Mitsuhiro Kainaga, Takuya Sasaki, Mizuki Kitamura, Takahiro Nakayama, Keita Masuda, Yukio Kakuta, Ichizo Nishino, Ichiro Imafuku
Publikováno v:
Internal Medicine. 62:797-802
Anti-mitochondrial antibody (AMA)-associated myopathies represent a homogeneous disease entity with severe arrhythmia and slowly progressive proximal muscle weakness with lordotic posture, irrespective of the presence of primary biliary cholangitis (
Autor:
Aki Kimura, Akimitsu Yamada, Yukako Shibata, Shiori Inoue, Masanori Oshi, Fumi Harada, Toshiaki Kadokura, Hideki Takeuchi, Naoki Hasegawa, Yukio Kakuta, Itaru Endo, Takashi Chishima
Publikováno v:
Gland Surgery. 11:1424-1430
Autor:
Hiromitsu Tannai, Kohzoh Makita, Yuya Koike, Haremaru Kubo, Kazuki Nakai, Yuto Yamazaki, Yuya Tsurutani, Jun Saito, Seishi Matsui, Yukio Kakuta, Hironobu Sasano, Tetsuo Nishikawa
Publikováno v:
Clinical endocrinology.
In patients with primary aldosteronism (PA), multiple adrenocortical nodules may be present on the surgical side. The aim of this study was to clarify the pathological diagnosis and the node-by-node diagnostic capability of segmental adrenal venous s
Autor:
Kazuhiro Takekoshi, Tetsuo Nishikawa, Naoki Hasegawa, Jun Saito, Masato Yonamine, Noriko Kimura, Kosuke Inoue, Chiho Sugisawa, Rei Hirose, Yukio Kakuta, Sachiko Suematsu, Yuya Tsurutani, Maki Nagata
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-8 (2021)
Journal of Medical Case Reports
Journal of Medical Case Reports
Background Pheochromocytoma and paraganglioma caused by succinate dehydrogenase gene mutations is called hereditary pheochromocytoma/paraganglioma syndrome. In particular, succinate dehydrogenase subunit B mutations are important because they are str
Autor:
Haruka Ito, Takeshi Kaneko, Hidetoshi Kawashima, Yukio Kakuta, Masaru Ito, Taketsugu Yamamoto, Takamitsu Maehara
Publikováno v:
Haigan. 60:109-114
Autor:
Haremaru Kubo, Yuya Tsurutani, Kosuke Inoue, Kazuki Watanabe, Yuto Yamazaki, Takashi Sunouchi, Yoshitomo Hoshino, Rei Hirose, Sho Katsuragawa, Hiromitsu Tannai, Yukiko Shibahara, Yukio Kakuta, Seishi Matsui, Jun Saito, Masao Omura, Hironobu Sasano, Tetsuo Nishikawa
Publikováno v:
PloS one. 17(4)
Primary aldosteronism (PA) usually accompanies suppressed plasma renin activity (PRA) through a negative feedback mechanism. While some cases of PA with unsuppressed PRA were reported, there have been no studies about the characteristics of PA with u
Autor:
Ikuko Mohri, Ayano Kuwada, Masaya Tachibana, Hiroaki Fushimi, Makoto Takeuchi, Masahiro Nakayama, Shigeo Murayama, Keiichi Ozono, Yukio Kakuta, Takeshi Inoue, Shihoko Kimura-Ohba, Ikuko Hirata, Kuriko Kagitani-Shimono, Masako Taniike, Masashi Shiomi
Publikováno v:
Brain and Development. 41:85-95
Background Influenza-associated encephalopathy (IAE) is one of the most serious CNS complications of an influenza virus infection, with unclear pathophysiology. Clasmatodendrosis is a complex of morphological changes in astrocytes characterized by fr