Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Naoko, YOKOTA"'
Autor:
Kazuaki Kinoshita, Yuichi Hoshino, Naoko Yokota, Masayuki Fukuda, Mika Hirata, Yuichiro Nishizawa
Publikováno v:
Heliyon, Vol 10, Iss 19, Pp e38717- (2024)
Objective: This prospective cohort study aimed to determine characteristics contributing to the development of Sever's disease in junior gymnasts. Methods: This study included 74 limbs from 37 junior gymnasts. The Baseline demographic data, flexibili
Externí odkaz:
https://doaj.org/article/e6d01b1a682e4801a08ab7fe50699752
Publikováno v:
Korean Journal of Transplantation, Vol 37, Iss 3, Pp 165-169 (2023)
Background : There are several procedural variations for kidney transplant donors, including open, laparoscopic, hand-assisted, and robotic methods, with either an intra- abdominal or retroperitoneal approach. Conversely, fewer options are available
Externí odkaz:
https://doaj.org/article/71bbc5cc03714f31899f041862039bfd
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-7 (2023)
Abstract Background Myocardial abscess is often associated with infective endocarditis (IE), and isolated myocardial abscess without IE is rare. Echocardiography and computed tomography (CT) are often used to diagnose myocardial abscess; however, to
Externí odkaz:
https://doaj.org/article/87a520bf22494c58a5dd03992d5ae097
Publikováno v:
JACC: Case Reports, Vol 29, Iss 3, Pp 102177- (2024)
The patient received endovascular therapy for a superficial femoral artery occlusion. Placement of a SMART stent distal to the lesion was successful, but deployment issues occurred with the Innova stent, requiring forceful retraction and causing elon
Externí odkaz:
https://doaj.org/article/4026e7027e5444a58509086c9b204d76
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-6 (2023)
Abstract Background Idiopathic chylopericardium is a rare disease characterized by filling of the pericardial cavity with chylous fluid and has no evident cause. Secondary chylopericardium usually results from injury or damage to the thoracic duct. T
Externí odkaz:
https://doaj.org/article/66e4e44a16cc455684f4f1f2a80190fe
Autor:
Ayako Kawabata, Tomoatsu Hayashi, Yoko Akasu-Nagayoshi, Ai Yamada, Naomi Shimizu, Naoko Yokota, Ryuichiro Nakato, Katsuhiko Shirahige, Aikou Okamoto, Tetsu Akiyama
Publikováno v:
Current Issues in Molecular Biology, Vol 44, Iss 4, Pp 1587-1596 (2022)
Epithelial ovarian cancer is classified into four major histological subtypes: serous, clear cell, endometrioid and mucinous. Ovarian clear cell carcinoma (OCCC) responds poorly to conventional chemotherapies and shows poor prognosis. Thus, there is
Externí odkaz:
https://doaj.org/article/da6dba27fdda494b9c8dfff75aa271d7
Autor:
Brandon Cona, Tomoatsu Hayashi, Ai Yamada, Naomi Shimizu, Naoko Yokota, Ryuichiro Nakato, Katsuhiko Shirahige, Tetsu Akiyama
Publikováno v:
FEBS Open Bio, Vol 12, Iss 3, Pp 582-593 (2022)
Certain cancers, such as ovarian clear cell carcinoma (OCCC), display high levels of genetic variation between patients, making it difficult to develop effective therapies. In order to identify novel genes critical to OCCC growth, we carried out a co
Externí odkaz:
https://doaj.org/article/fee9bc37aa154de78549a667a47d55cf
Publikováno v:
Medicina, Vol 59, Iss 6, p 1161 (2023)
Background and objective: Unilateral agenesis of pulmonary arteries (UAPA) is a rare disease, with approximately 400 cases reported to date. UAPA is often associated with congenital heart disease, and the uncomplicated form is isolated UAPA, which ac
Externí odkaz:
https://doaj.org/article/3a3ae77b69c748229664e641c4299ce3
Autor:
Naoko Yokota‐Nakagi, Sayo Omoto, Shoko Tazumi, Mizuho Kawakami, Akira Takamata, Keiko Morimoto
Publikováno v:
Physiological Reports, Vol 10, Iss 5, Pp n/a-n/a (2022)
Abstract The role of 17β‐estradiol (E2) in high‐fat diet (HFD)‐induced alteration of the protein kinase B (Akt) signaling pathway in ovariectomized (OVX) rats is unclear. Therefore, we examined whether chronic estrogen replacement restores HFD
Externí odkaz:
https://doaj.org/article/d36895d35aa24bac9fd089e6d8171e8c
Autor:
Marohito Nakata, Naoko Yokota, Kazuhiko Tabata, Takuya Morikawa, Hiroki Shibata, Tsuneaki Kenzaka
Publikováno v:
Medicina, Vol 59, Iss 3, p 615 (2023)
Background: Cardiopulmonary disorders are the most common cause of central cyanosis, and methemoglobinemia is often overlooked in the differential diagnosis of patients with central cyanosis. In most cases, methemoglobinemia is acquired and hereditar
Externí odkaz:
https://doaj.org/article/d9bc5b332f8a44eba445f2e42f5fd56b