Zobrazeno 1 - 10
of 216
pro vyhledávání: '"Akinari, Fukuda"'
Autor:
Ryutaro Tamura, Yusuke Sabu, Tadahaya Mizuno, Seiya Mizuno, Satoshi Nakano, Mitsuyoshi Suzuki, Daiki Abukawa, Shunsaku Kaji, Yoshihiro Azuma, Ayano Inui, Tatsuya Okamoto, Seiichi Shimizu, Akinari Fukuda, Seisuke Sakamoto, Mureo Kasahara, Satoru Takahashi, Hiroyuki Kusuhara, Yoh Zen, Tomohiro Ando, Hisamitsu Hayashi
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract Choline is an essential nutrient, and its deficiency causes steatohepatitis. Dietary phosphatidylcholine (PC) is digested into lysoPC (LPC), glycerophosphocholine, and choline in the intestinal lumen and is the primary source of systemic cho
Externí odkaz:
https://doaj.org/article/6e3497d067f34e50bfe570fb76233f5d
Autor:
Yusuke Yanagi, MD, PhD, Seisuke Sakamoto, MD, PhD, Masaki Yamada, MD, PhD, Koutaro Mimori, MD, Toshimasa Nakao, MD, PhD, Tasuku Kodama, MD, PhD, Hajime Uchida, MD, PhD, Seiichi Shimizu, MD, PhD, Akinari Fukuda, MD, PhD, Noriyuki Nakano, MD, PhD, Chiduko Haga, MD, PhD, Takako Yoshioka, MD, PhD, Mureo Kasahara, MD, PhD
Publikováno v:
Transplantation Direct, Vol 8, Iss 9, p e1359 (2022)
Background. The management and outcome of ABO-incompatible (ABO-I) liver transplantation (LT) has been improving over the past few decades. Recently, the introduction of a pathological evaluation of acute antibody-mediated rejection (AMR) for liver a
Externí odkaz:
https://doaj.org/article/d52c0b0777e14b56952d7f28c5e77bd9
Autor:
Masaru Shimura, Naomi Kuranobu, Minako Ogawa-Tominaga, Nana Akiyama, Yohei Sugiyama, Tomohiro Ebihara, Takuya Fushimi, Keiko Ichimoto, Ayako Matsunaga, Tomoko Tsuruoka, Yoshihito Kishita, Shuichiro Umetsu, Ayano Inui, Tomoo Fujisawa, Ken Tanikawa, Reiko Ito, Akinari Fukuda, Jun Murakami, Shunsaku Kaji, Mureo Kasahara, Kazuo Shiraki, Akira Ohtake, Yasushi Okazaki, Kei Murayama
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Hepatocerebral mitochondrial DNA depletion syndrome (MTDPS) is a disease caused by defects in mitochondrial DNA maintenance and leads to liver failure and neurological complications during infancy. Liver transplantation (LT) remai
Externí odkaz:
https://doaj.org/article/e45f0df00481472298ff7a0e4c4c93cf
Autor:
Kensuke Shoji, Jumpei Saito, Hidenori Nakagawa, Takanori Funaki, Akinari Fukuda, Seisuke Sakamoto, Mureo Kasahara, Jeremiah D. Momper, Edmund V. Capparelli, Isao Miyairi
Publikováno v:
Microbiology Spectrum, Vol 9, Iss 2 (2021)
ABSTRACT Methicillin-resistant Staphylococcus aureus infections are a significant cause of morbidity and mortality in pediatric liver transplant (LT) recipients. Physiological changes following LT may affect vancomycin pharmacokinetics; however, appr
Externí odkaz:
https://doaj.org/article/87a74edb86db42bca17204276cec3163
Autor:
Jumpei Saito, Miho Yamaguchi, Seiichi Shimizu, Kyoko Chiba, Tomoyuki Utano, Akinari Fukuda, Seisuke Sakamoto, Mureo Kasahara, Akimasa Yamatani
Publikováno v:
Children, Vol 9, Iss 10, p 1598 (2022)
Sulfamethoxazole trimethoprim (ST) combinations are used to prevent infection in immunocompromised patients. In pediatric patients, conventional ST combination tablets (cTab) are large and granules are not preferred due to their rough and bitter tast
Externí odkaz:
https://doaj.org/article/a1651484a43e41fe90c9e4e4d109e3d4
Autor:
Kensuke Shoji, Jumpei Saito, Yusuke Oho, Shotaro Matsumoto, Satoshi Aoki, Akinari Fukuda, Seisuke Sakamoto, Mureo Kasahara, Edmund Capparelli, Isao Miyairi
Publikováno v:
Clinical Case Reports, Vol 7, Iss 11, Pp 2169-2173 (2019)
Abstract We report on an 8‐year‐old girl with Wilson disease who developed three episodes of peritonitis due to extended‐spectrum beta‐lactamase‐producing Escherichia coli after liver transplantation. Massive ascites were thought to account
Externí odkaz:
https://doaj.org/article/352bf210d8e84d58a4e8124a1dbd1a7a
Autor:
Tomonori Tsuchida, Soichiro Murata, Shunsuke Hasegawa, Satoshi Mikami, Shin Enosawa, Huai-Che Hsu, Akinari Fukuda, Satoshi Okamoto, Akihiro Mori, Megumi Matsuo, Yumi Kawakatsu, Hitomi Matsunari, Kazuaki Nakano, Hiroshi Nagashima, Hideki Taniguchi
Publikováno v:
Cell Transplantation, Vol 29 (2020)
Transplantation of liver organoids has been investigated as a treatment alternative to liver transplantation for chronic liver disease. Transportal approach can be considered as a method of delivering organoids to the liver. It is important to set th
Externí odkaz:
https://doaj.org/article/e5a15e8cd9664e689aa359ae7fea233c
Autor:
Hisamitsu Hayashi, Sotaro Naoi, Takao Togawa, Yu Hirose, Hiroki Kondou, Yasuhiro Hasegawa, Daiki Abukawa, Mika Sasaki, Koji Muroya, Satoshi Watanabe, Satoshi Nakano, Kei Minowa, Ayano Inui, Akinari Fukuda, Mureo Kasahara, Hironori Nagasaka, Kazuhiko Bessho, Mitsuyoshi Suzuki, Hiroyuki Kusuhara
Publikováno v:
EBioMedicine, Vol 27, Iss C, Pp 187-199 (2018)
Progressive familial intrahepatic cholestasis type 1 (PFIC1), a rare inherited recessive disease resulting from a genetic deficiency in ATP8B1, progresses to liver failure. Because of the difficulty of discriminating PFIC1 from other subtypes of PFIC
Externí odkaz:
https://doaj.org/article/ce1e9672a010451aaf8a48d29e6a166a
Autor:
Sapana Verma, Seisuke Sakamoto, Abdelwahed, Mohamed Sami, Seiichi Shimizu, Hajime Uchida, Noriki Okada, Toshimasa Nakao, Tasuku Kodama, Ryuji Komine, Akinari Fukuda, Mohamed Rela, Mureo Kasahara
Publikováno v:
Liver Transplantation; Jan2024, Vol. 30 Issue 1, p103-106, 4p
Autor:
Mureo, Kasahara, Seisuke, Sakamoto, Akinari, Fukuda, Hajime, Uchida, Nam-Joon, Yi, Andrea, Schlegel, Paolo, Muiesan, Xia, Qiang, Wei, Gao, Zhi-Jun, Zhu, Manuel, Rodriguez-Davalos, Mohamed, Rela
Publikováno v:
Current Opinion in Organ Transplantation. 27:346-350
Living donor liver transplantation (LT) has been increasingly recognized as an effective treatment modality with excellent patient survival. Indications for LT have evolved not only for cholestatic liver disease, but also metabolic liver diseases. Li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::559d218b1cc198ae2b09e4d7f515b97d
https://doi.org/10.1097/mot.0000000000000990
https://doi.org/10.1097/mot.0000000000000990