Zobrazeno 1 - 10
of 175
pro vyhledávání: '"Hiroko, Kodama"'
Autor:
Makoto Kodama, Soh Okano, Shuko Nojri, Keiko Abe, Masayuki Fukata, Yoshihiro Nagase, Hiroko Kodama
Publikováno v:
PLoS ONE, Vol 19, Iss 5, p e0300580 (2024)
Although a Western diet has been identified as a risk factor for Crohn's disease (CD), there is still controversy surrounding the specific foods that may contribute to the development of the disease. In this study, we examined the association between
Externí odkaz:
https://doaj.org/article/d6d2e9f4fb064363a698d00f65b9f9e7
Autor:
Chie Fujisawa, Hiroko Kodama, Yasuhiro Sato, Masakazu Mimaki, Mariko Yagi, Hiroyuki Awano, Muneaki Matsuo, Haruo Shintaku, Sayaka Yoshida, Masaki Takayanagi, Mitsuru Kubota, Akihito Takahashi, Yoshikiyo Akasaka
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 31, Iss , Pp 100849- (2022)
Menkes disease (MD) is an X-linked recessive disorder caused by mutations in ATP7A. Patients with MD exhibit severe neurological and connective tissue disorders due to copper deficiency and typically die before 3 years of age. Early treatment with co
Externí odkaz:
https://doaj.org/article/f8c4161e9892446a81dc2393c238b3f6
Autor:
Kyoko Nomura, Yuki Itakura, Sachiko Minamizono, Kazuyo Okayama, Yumiko Suzuki, Yukari Takemi, Akemi Nakanishi, Kumi Eto, Hitoshi Takahashi, Yuki Kawata, Hitomi Asakura, Yorika Matsuda, Naoko Kaibara, Sakiko Hamanaka, Hiroko Kodama
Publikováno v:
Frontiers in Psychology, Vol 12 (2021)
Background: Body image self-discrepancy reflects a preference for weight loss regardless of normal body size and is a distorted cognition that may be a precursor to eating disorders. The aim of this study was to investigate factors associated with bo
Externí odkaz:
https://doaj.org/article/69544c7d889b4aad87465d4690ed232e
Publikováno v:
BMJ Paediatrics Open, Vol 5, Iss 1 (2021)
Objective To evaluate the concentrations of copper and zinc in the breast milk of mothers undergoing treatment for Wilson’s disease (WD) and clarify whether they can safely breast feed their infants.Design This was an observational and prospective
Externí odkaz:
https://doaj.org/article/3530dedf9e9747e7b38bb53ee1fa18df
Autor:
Minoru Yasukawa, Shigeyuki Arai, Michito Nagura, Ryo Kido, Shinichiro Asakawa, Daigoro Hirohama, Osamu Yamazaki, Yoshifuru Tamura, Michitaka Fujimaki, Sawako Kobayashi, Masakazu Mimaki, Hiroko Kodama, Shunya Uchida, Yoshihide Fujigaki, Shigeru Shibata
Publikováno v:
Kidney International Reports. 7:1565-1574
Impaired response to erythropoiesis-stimulating agents (ESAs) is associated with increased mortality in patients with end-stage kidney disease. However, the underlying mechanisms are not fully elucidated. Accumulating data reveal that selenium (Se),
Autor:
Takahiro Matsuki, Kana Yahagi, Hiroshi Mori, Hoshitaka Matsumoto, Taeko Hara, Saya Tajima, Eishin Ogawa, Hiroko Kodama, Kazuya Yamamoto, Takuji Yamada, Satoshi Matsumoto, Ken Kurokawa
Publikováno v:
Nature Communications, Vol 7, Iss 1, Pp 1-12 (2016)
The factors shaping the development of infants' gut microbiota are poorly understood. Here, the authors show that alterations in gut microbiota development in infants are associated with the presence of bifidobacteria having a gene for utilisation of
Externí odkaz:
https://doaj.org/article/6bc1bcb4578842b29ebd9ba9c24ac85e
Autor:
Masao Kumode, Ryo Sumimoto, Takafumi Miyachi, Masami Yamasaki, Hiroko Kodama, Masahiko Takemoto, Hiromitsu Ohmori, Tomio Matsumoto
Publikováno v:
World Journal of Clinical Cases
BACKGROUND Percutaneous endoscopic gastrostomy with jejunal extension (PEG-J) is often used to treat patients with neurological impairment and difficulty in swallowing. However, these patients often develop copper deficiency. This report describes a
Autor:
Kiyomi Ito, Yoshiaki Yamagishi, Taiki Akashi, Shohei Kobayashi, Toshiyuki Kudo, Takeaki Kawakami, Hideyo Takahashi, Yasuhiro Sato, Masafumi Oyumi, Kosho Makino, Masakazu Mimaki, Hitomi Goda, Mitsutoshi Munakata, Hiroko Kodama, Toshiro Fukami, Kazuki Takahashi, Yusuke Sakamoto
Publikováno v:
Pharmaceutical Research. 38:1335-1344
Menkes disease is a rare hereditary disease in which systemic deficiency of copper due to mutation of the ATP7A gene causes severe neurodegenerative disorders. The present parenteral drugs have limited efficacy, so there is a need for an efficacious
Autor:
Yasuhiro Sato, Hiroko Kodama, Tsuyoshi Isojima, Haruko Hiraike, Yuko Hino, Masakazu Mimaki, Kahoko Motoyama, Kyoko Nomura, Ayaka Aihara, Hitomi Asakura
Publikováno v:
Pediatrics International. 63:910-917
BACKGROUND Many trace elements are essential for infant growth and development during early life. Their concentrations in breast milk vary depending on social and economic factors. Nonetheless, the present available values in Japan were derived from
Autor:
Daiki Ogishima, Asumi Sakaguchi, Hiroko Kodama, Kanako Ogura, Ayako Miwa, Yayoi Sugimori, Shozo Matuoka, Toshiharu Matsumoto
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2017 (2017)
A supernumerary ovary is an exceedingly rare disorder, in which the structure containing ovarian tissue is located at some distance from the normally placed ovary. 16 cases of endometriosis or tumors originating in a supernumerary ovary have been pub
Externí odkaz:
https://doaj.org/article/9a41891a04604a80ad267642d95d8bfa