8 件中 1 - 8 件目
英語 ：Masayo Yamamoto, Motohiro Shindo, Takuya Funayama, Chihiro Sumi, Takeshi Saito, Yasumichi Toki, Mayumi Hatayama, Ken-Ichi Imadome, Yusuke Mizukami, Toshikatsu Okumura , Late-onset posttransplant Epstein-Barr virusrelated lymphoproliferative disease after cord blood transplantation for chronic active Epstein Barr virus infection: A case report , Medicine (Baltimore) , 2022
英語 ：Sohji Nishina, Yasuyuki Tomiyama, Katsuya Ikuta, Yasuaki Tatsumi, Yasumichi Toki, Ayako Kato, Koichi Kato, Naoko Yoshioka, Kyo Sasaki, Yuichi Hara, Keisuke Hino , Long-term phlebotomy successfully alleviated hepatic iron accumulation in a ferroportin disease patient with a mutation in SLC40A1: a case report , BMC Gastroenterology , 2021
英語 ：Honma Y, Karasuyama T, Kumamoto K, Shimajiri S, Toki Y, Tatsumi Y, Sumida K, Koikawa K, Morino K, Oe S, Miyagawa K, Yamasaki M, Shibata M, Abe S, Ikuta K, Hayashi H, Harada M. , Share Type 4B hereditary hemochromatosis due to heterozygous p.D157A mutation in SLC40A1 complicated with hypopituitarism. , Medical Molecular Morphology , 2021
英語 ：Yamamoto M, Shindo M, Sumi C, Igarashi S, Saito T, Tsukada N, Toki Y, Hatayama M, Inamura J, Sato K, Mizukami Y, Torimoto Y, Okumura T. , Acquired hemophilia A associated with Epstein-Barr-virus-associated T/natural killer-cell lymphoproliferative disease: A case report. , Medicine(Baltimore), 100 (16) , 2021
英語 ：Igarashi S, Nozu T, Ishioh M, Kumei S, Saito T, Toki Y, Hatayama M, Yamamoto M, Shindo M, Tanabe H, Okumura T. , Centrally administered orexin prevents lipopolysaccharide and colchicine induced lethality via the vagal cholinergic pathway in a sepsis model in rats , Biochemical Pharmacology , 2020
英語 ：akami A, Tatsumi Y, Sakai K, Toki Y, Ikuta K, Oohigashi Y, Takagi J, Kato K, Takami K. , Juvenile Hemochromatosis: A Case Report and Review of the Literature. , Pharmaceuticals , 2020
英語 ：Kawaguchi T, Ikuta K, Tatsumi Y, Toki Y, Hayashi H, Tonan T, Ohtake T, Hoshino S, Naito M, Kato K, Okumura T, Torimura T. , Identification of heterozygous p.Y150C and p.V274M mutations in the HJV gene in a Japanese patient with a mild phenotype of juvenile hemochromatosis: A case report. , Hepatology Reseach , 2020
日本語 ：西尾 仁, 本間 雄一, 熊元 啓一郎, 土岐 康通, 森野 加帆里, 大江 晋司, 宮川 恒一郎, 柴田 道彦, 阿部 慎太郎, 巽 康彰, 生田 克哉, 林 久男, 原田 大 , TfR2ヘテロ接合型変異で発症したヘモクロマトーシスの1例 , 肝臓 , 2022
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