Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Takao Togawa"'
Autor:
Midori Obayashi, Sachiko Iwata, Tomoya Okuda, Ichita Mori, Shigeharu Nakane, Yasuko Togawa, Mari Sugimoto, Takao Togawa, Kanji Muramatsu, Shinji Saitoh, Takahiro Sugiura, Osuke Iwata
Publikováno v:
Nutrients, Vol 16, Iss 4, p 476 (2024)
Early enteral nutrition using reliable biomarkers of intestinal function must be established to improve neurodevelopmental outcomes in very low birth weight infants (VLBWIs). Serum citrulline levels reflect the intestinal function in adults. To eluci
Externí odkaz:
https://doaj.org/article/39eb20ceb1834418a213865c5c5e6f0a
Autor:
Yoshinori Satomura, Kazuhiko Bessho, Nobutoshi Nawa, Hidehito Kondo, Shogo Ito, Takao Togawa, Masanao Yano, Yuki Yamano, Taisuke Inoue, Miho Fukui, Shinsuke Onuma, Tomoya Fukuoka, Kie Yasuda, Takeshi Kimura, Makiko Tachibana, Taichi Kitaoka, Shin Nabatame, Keiichi Ozono
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-6 (2022)
Abstract Background Arthrogryposis, renal dysfunction, and cholestasis syndrome (ARCS) is a rare autosomal recessive disorder caused by mutations in VPS33B (ARCS1) and VIPAS39 (ARCS2). As per literature, most patients with ARCS died of persistent inf
Externí odkaz:
https://doaj.org/article/ac1143801be74e5f85e9d7f8ee61ab4c
Autor:
Ken Kato, Shuichiro Umetsu, Takao Togawa, Koichi Ito, Takayoshi Kawabata, Teruko Arinaga-Hino, Naoya Tsumura, Ryosuke Yasuda, Yutaro Mihara, Hironori Kusano, Shogo Ito, Kazuo Imagawa, Hisamitsu Hayashi, Ayano Inui, Yushiro Yamashita, Tatsuki Mizuochi
Publikováno v:
Journal of Clinical Medicine, Vol 12, Iss 18, p 5979 (2023)
Background: Few reports of benign recurrent intrahepatic cholestasis (BRIC) have focused on East Asian patients. We describe the clinicopathologic features, genetics, treatment, and outcomes in Japanese BRIC patients. Methods: We recruited patients w
Externí odkaz:
https://doaj.org/article/b3f0a8b507ee4494bbabce0820ca44ba
Autor:
Chiyoe Shirota, Akinari Hinoki, Takao Togawa, Shogo Ito, Wataru Sumida, Satoshi Makita, Hizuru Amano, Aitaro Takimoto, Shunya Takada, Masamune Okamoto, Yoichi Nakagawa, Daiki Kato, Hiroo Uchida
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundThe prognosis of BA is known to be poor if definitive surgery is performed too late. Therefore, excluding BA as a diagnosis at an early stage is crucial. Conventional cholangiography requiring cannulation through the gallbladder may be unne
Externí odkaz:
https://doaj.org/article/fca2e8b035484affa483fb0c613aa61f
Autor:
Hiroyuki Suzuki, Teruko Arinaga-Hino, Tomoya Sano, Yutaro Mihara, Hironori Kusano, Tatsuki Mizuochi, Takao Togawa, Shogo Ito, Tatsuya Ide, Reiichiro Kuwahara, Keisuke Amano, Toshihiro Kawaguchi, Hirohisa Yano, Masayoshi Kage, Hironori Koga, Takuji Torimura
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Benign recurrent intrahepatic cholestasis type 1 (BRIC1) is a rare autosomal recessive disorder that is characterized by intermittent episodes of jaundice and intense pruritus and caused by pathogenic variants of adenosine triphosphatase phospholipid
Externí odkaz:
https://doaj.org/article/273337d8cf2a4d5f9cc9e33997d0884e
Autor:
Syunsuke Nagara, Masanori Kouwaki, Takao Togawa, Tokio Sugiura, Mayumi Okada, Norihisa Koyama
Publikováno v:
Pediatrics and Neonatology, Vol 59, Iss 3, Pp 274-280 (2018)
Marked improvements have been achieved in the survival of extremely low birth weight infants, but survival rates and prognoses of extremely small infants with birth weights ≤500 g remain poor. The aim of this study was to clarify long-term outcomes
Externí odkaz:
https://doaj.org/article/371afc63d51a4baa8f51cc1a2fc7b790
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:
Takanori Suzuki, Kentaro Matsuura, Naoto Imura, Hayato Kawamura, Kayoko Kuno, Kei Fujiwara, Shunsuke Nojiri, Shogo Ito, Takao Togawa, Hiromi Kataoka
Publikováno v:
Internal Medicine; 2024, Vol. 63 Issue 6, p833-837, 5p
Autor:
Shinji Saitoh, Masanori Kouwaki, Hitoshi Kanno, Hiromi Ogura, Takahiro Sugiura, Tomoko Suzuki, Toshiyuki Yamamoto, Takao Togawa
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:e250-e254
Hereditary pyropoikilocytosis is a subtype of hereditary elliptocytosis because of biallelic mutations of SPTA1, SPTB, and EPB41. The authors present a proband with neonatal jaundice and hemolytic anemia, with poikilocytosis in the blood film. Target
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 64(1)