Hasil Pencarian - Hisamitsu Hayashi

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  1. 1
    The Long-Term Efficacy of Cochlear Implantation for Hearing Loss in Muckel-Wells Syndrome

    The Long-Term Efficacy of Cochlear Implantation for Hearing Loss in Muckel-Wells Syndrome oleh Bakushi Ogawa, Mitsuhiro Aoki, Hidenori Ohnishi, Toshimitsu Ohashi, Hisamitsu Hayashi, Bunya Kuze, Yatsuji Ito

    Diterbitkan 2019-12-01
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  2. 2
    Biphenotypic siononasal sarcoma with acute exacerbation: A case report

    Biphenotypic siononasal sarcoma with acute exacerbation: A case report oleh Hiroshi Okuda, Bunya Kuze, Hirofumi Shibata, Hisamitsu Hayashi, Takesumi Nishihori, Keisuke Mizuta, Keishi Kohyama, Yuji Yasue, Hisakazu Kato, Mitsuhiro Aoki

    Diterbitkan 2020-09-01
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  3. 3
    Navigating cholestasis: identifying inborn errors of bile acid metabolism for precision diagnosis

    Navigating cholestasis: identifying inborn errors of bile acid metabolism for precision diagnosis oleh Hiroshi Nittono, Mitsuyoshi Suzuki, Hiromi Suzuki, Hiromi Suzuki, Satoru Sugimoto, Jun Mori, Rieko Sakamoto, Yugo Takaki, Hisamitsu Hayashi, Hajime Takei, Akihiko Kimura

    Diterbitkan 2024-04-01
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  4. 4
    Influence of food on pharmacokinetics and pharmacodynamics of 4-phenylbutyrate in patients with urea cycle disorders

    Influence of food on pharmacokinetics and pharmacodynamics of 4-phenylbutyrate in patients with urea cycle disorders oleh Yoko Nakajima, Shuhei Osaka, Tadahaya Mizuno, Katsuyuki Yokoi, Satoshi Nakano, Saeko Hirai, Yuka Hiraoka, Yoshiki Miura, Mitsuyoshi Suzuki, Hiroyuki Kusuhara, Hisamitsu Hayashi

    Diterbitkan 2021-12-01
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  5. 5
    Clinical symptoms, biochemistry, and liver histology during the native liver period of progressive familial intrahepatic cholestasis type 2

    Clinical symptoms, biochemistry, and liver histology during the native liver period of progressive familial intrahepatic cholestasis type 2 oleh Hiroki Kondou, Satoshi Nakano, Tadahaya Mizuno, Kazuhiko Bessho, Yasuhiro Hasegawa, Atsuko Nakazawa, Ken Tanikawa, Yoshihiro Azuma, Tatsuya Okamoto, Ayano Inui, Kazuo Imagawa, Mureo Kasahara, Yoh Zen, Mitsuyoshi Suzuki, Hisamitsu Hayashi

    Diterbitkan 2024-02-01
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  6. 6
    Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages

    Assessment of ATP8B1 Deficiency in Pediatric Patients With Cholestasis Using Peripheral Blood Monocyte-Derived Macrophages oleh 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

    Diterbitkan 2018-01-01
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  7. 7
    Intestinal Atp8b1 dysfunction causes hepatic choline deficiency and steatohepatitis

    Intestinal Atp8b1 dysfunction causes hepatic choline deficiency and steatohepatitis oleh 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

    Diterbitkan 2023-11-01
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  8. 8
    Human iPSC-derived hepatocyte system models cholestasis with tight junction protein 2 deficiency

    Human iPSC-derived hepatocyte system models cholestasis with tight junction protein 2 deficiency oleh Chao Zheng Li, Hiromi Ogawa, Soon Seng Ng, Xindi Chen, Eriko Kishimoto, Kokoro Sakabe, Aiko Fukami, Yueh-Chiang Hu, Christopher N. Mayhew, Jennifer Hellmann, Alexander Miethke, Nahrin L. Tasnova, Samuel J.I. Blackford, Zu Ming Tang, Adam M. Syanda, Liang Ma, Fang Xiao, Melissa Sambrotta, Oliver Tavabie, Filipa Soares, Oliver Baker, Davide Danovi, Hisamitsu Hayashi, Richard J. Thompson, S. Tamir Rashid, Akihiro Asai

    Diterbitkan 2022-04-01
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  9. 9
    Clinical and genetic features of congenital bile acid synthesis defect with a novel mutation in AKR1D1 gene sequencing

    Clinical and genetic features of congenital bile acid synthesis defect with a novel mutation in AKR1D1 gene sequencing oleh Anh-Hoa Nguyen Pham, MD, PhD, Kim-Oanh Bui Thi, MD, Mai-Huong Nguyen Thi, MD, Diem-Ngoc Ngo, MD, Nakayuki Naritaka, MD, Hiroshi Nittono, MD, Hisamitsu Hayashi, MD, Trang Thi Dao, MD, Kim-Huong Thi Nguyen, MD, Hoai-Nghia Nguyen, PhD, Hoa Giang, PhD, Hung-Sang Tang, MD, Tat-Thanh Nguyen, MD, Dinh-Kiet Truong, PhD, Minh-Dien Tran, MD

    Diterbitkan 2022-06-01
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