Papers
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Three Consecutive Cases of Familial Hemophagocytic Lymphohistiocytosis, Including a Case Due to Maternal Uniparental Disomy, J Pediatr Hematol Oncol, 42(8) e819-e821, 2020
Hiroko Sato, Tetsuo Mitsui et al
Multiple Authorship (Only Japanese)
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Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs, Journal of Human Genetics, 2015
Hiroko Sato, Toshihiko Uchida, Kiyoshi Hayasaka et al
Multiple Authorship (Only Japanese)
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Association of breast-fed neonatal hyperbilirubinemia with UGT1A1 polymorphisms: 211G>A(G71R) mutation becomes a risk factor under inadequate feeding, Journal of Human Genetics, 2012
Hiroko Sato, Toshihiko Uchida, Kiyoshi Hayasaka et al
Multiple Authorship (Only Japanese)
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Colorectal cancer in a patient with glutaric aciduria type 1, Pediatrics International, 2024
Kiyoshi Hayasaka MD, PhD, Chikahiko Numakura MD, PhD, Hiroko Sato MD, PhD, Toru Meguro MD, PhD, Tetsuo Mitsui MD, PhD
Multiple Authorship (Only Japanese)
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ALOX12 mutation in a family with dominantly inherited bleeding diathesis, Journal of Human Genetics, 2020
Tetsuo Mitsui, Satoshi Makino, Gen Tamiya, Hiroko Sato, Yuki Kawakami, Yoshitaka Takahashi, Toru Meguro, Hiroko Izumino, Yosuke Sudo, Ikuo Norota, Kuniaki Ishii, Kiyoshi Hayasaka
Multiple Authorship (Only Japanese)
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Eltrombopag with i.v. immunoglobulin for safe splenectomy in refractory immune thrombocytopenia, Pediatrics International, 2018
Miyako Kanno, Tadashi Onoda, Tohru Meguro, Hiroko Sato, Tetsuo Mitsui
Multiple Authorship (Only Japanese)