Kanno Hitoshi

カンノヒトシ | Kanno Hitoshi

Research field (1)： Hematology and oncology

Research theme for competitive and other funds (20)：

2020 - 2023 Biochemical characteristics of erythrocytes in extremely preterm infants and identification of loci conferring susceptibility to prolonged severe hyperbilirubinemia
2016 - 2020 Pathological analysis of congenital hemolytic anemia due to mitochondrial selective autophagy disorder
2013 - 2017 Comprehensive analysis of genetic polymorphisms and irinotecan-induced adverse events in Japanese gastrointestinal cancer patients: a DMET microarray profiling study
2013 - 2016 Identification of novel pathogenic genes for congenital hemolytic anemia and establishment of comprehensive gene testing
2012 - 2014 新規複合的アプローチによる腎細胞癌に対するγδ型T細胞傷害活性増強効果の検討

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Papers (64)：

Erina Nakahara, Keiko Shimojima Yamamoto, Hiromi Ogura, Takako Aoki, Taiju Utsugisawa, Kenko Azuma, Hiroyuki Akagawa, Kenichiro Watanabe, Michiko Muraoka, Fumihiko Nakamura, et al. Variant spectrum of PIEZO1 and KCNN4 in Japanese patients with dehydrated hereditary stomatocytosis. Human genome variation. 2023. 10. 1. 8-8
Motoshi Sonoda, Masataka Ishimura, Yuko Ichimiya, Eiko Terashi, Katsuhide Eguchi, Yasunari Sakai, Hidetoshi Takada, Asahito Hama, Hitoshi Kanno, Tsutomu Toki, et al. Correction to: Atypical erythroblastosis in a patient with Diamond-Blackfan anemia who developed del(20q) myelodysplasia. International journal of hematology. 2018. 108. 2. 236-236
Takuya Ichimura, Kenichi Yoshida, Yusuke Okuno, Toshiaki Yujiri, Kozo Nagai, Masanori Nishi, Yuichi Shiraishi, Hiroo Ueno, Tsutomu Toki, Kenichi Chiba, et al. Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing. International journal of hematology. 2017. 105. 4. 515-520
Fumika Ikeda, Kenichi Yoshida, Tsutomu Toki, Tamayo Uechi, Shiori Ishida, Yukari Nakajima, Yoji Sasahara, Yusuke Okuno, Rika Kanezaki, Kiminori Terui, et al. Exome sequencing identified RPS15A as a novel causative gene for Diamond-Blackfan anemia. Haematologica. 2017. 102. 3. e93-e96
Hidetaka Niizuma, Hitoshi Kanno, Atsushi Sato, Hiromi Ogura, Masue Imaizumi. Splenectomy resolves hemolytic anemia caused by adenylate kinase deficiency. Pediatrics international : official journal of the Japan Pediatric Society. 2017. 59. 2. 228-230

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MISC (280)：

菅野仁, 槍澤大樹. ヘモグロビン異常症. 日本輸血細胞治療学会誌. 2021. 67. 2
久保田友晶, 松田和樹, 守屋友美, 及川美幸, 木下明美, 千野峰子, 岡田真一, 高源ゆみ, 青木正弘, 中林恭子, et al. 皮下注用人免疫グロブリンの在宅自己注射における投与記録管理の問題点. 日本輸血細胞治療学会誌. 2021. 67. 2
守屋友美, 松田和樹, 久保田友晶, 及川美幸, 木下明美, 千野峰子, 岡田真一, 高源ゆみ, 青木正弘, 中林恭子, et al. 災害時の院内における血液製剤管理と供給体制. 日本輸血細胞治療学会誌. 2021. 67. 2
中原衣里菜, 中原衣里菜, 菅野仁, 山本俊至, 谷ヶ崎博, 森岡一朗. Rapid Diagnosis Method for Hemolytic Disease of the Newborn-Quantitative Erythrocyte Osmotic Fragility Test. 日本小児科学会雑誌. 2021. 125. 2
牧野茂義, 菅野仁, 岡本好雄, 北澤淳一, 山本晃士, 安村敏, 米村雄士, 横濱章彦, 松下正. 改善されてきたわが国の輸血医療,その現状と課題. 日本輸血細胞治療学会誌. 2021. 67. 2

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Awards (2)：

1995/10 - 日本人類遺伝学会奨励賞ピルビン酸キナーゼ異常による遺伝性溶血性貧血症の病因に関する分子遺伝学的解析
1994/04 - 日本血液学会奨励賞

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