Rchr
J-GLOBAL ID：201601015616640519
Update date: Mar. 07, 2024
Sasai Hideo
ササイ ヒデオ | Sasai Hideo
Affiliation and department：
Research field (2)：
Fetal medicine/Pediatrics
, Metabolism and endocrinology
Research keywords (2)：
Inborn errors of ketone body metabolism
, Inborn errors of metabolism
Research theme for competitive and other funds (4)：
- 2022 - 2025 Developments of comprehensive diagnosis and analysis systems for disorders of ketone body metabolism
- 2019 - 2021 Molecular and functional analysis of HSD 10 disease
- 2017 - 2019 Functional analysis of HSD 10 disease
- 2016 - 2019 Research on defects in ketone body metabolism: Establishment of defective cell lines and expression systems of mutant enzymes .
Papers (54)：
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Go Tajima, Junko Aisaki, Keiichi Hara, Miyuki Tsumura, Reiko Kagawa, Fumiaki Sakura, Hideo Sasai, Miori Yuasa, Yosuke Shigematsu, Satoshi Okada. Using the C14:1/Medium-Chain Acylcarnitine Ratio Instead of C14:1 to Reduce False-Positive Results for Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency in Newborn Screening in Japan. International Journal of Neonatal Screening. 2024
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Go Tajima, Keiichi Hara, Miyuki Tsumura, Reiko Kagawa, Fumiaki Sakura, Hideo Sasai, Miori Yuasa, Yosuke Shigematsu, Satoshi Okada. Newborn Screening with (C16 + C18:1)/C2 and C14/C3 for Carnitine Palmitoyltransferase II Deficiency throughout Japan Has Revealed C12/C0 as an Index of Higher Sensitivity and Specificity. International Journal of Neonatal Screening. 2023
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市野井 那津子, 高野 智圭, 小川 えりか, 石井 和嘉子, 小林 正久, 笹井 英雄, 岡崎 康司, 村山 圭, 森岡 一朗, 石毛 美夏. 新生児マススクリーニングでC3とC5-OH上昇を示した乳児期発症Leigh脳症の一例. 日本マス・スクリーニング学会誌. 2023. 33. 2. 228-228
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Nanako Omichi, Yoshihito Kishita, Mina Nakama, Hideo Sasai, Atsushi Terazawa, Emiko Kobayashi, Takuya Fushimi, Yohei Sugiyama, Keiko Ichimoto, Kazuhiro R Nitta, et al. Novel ITPA variants identified by whole genome sequencing and RNA sequencing. Journal of human genetics. 2023. 68. 9. 649-652
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Daiki Nagao, Michio Ozeki, Akifumi Nozawa, Shiho Yasue, Hideo Sasai, Saori Endo, Takazumi Kato, Yumiko Hori, Hidenori Ohnishi. A Case of Multifocal Lymphangioendotheliomatosis With Thrombocytopenia and Changes in Coagulopathy. Journal of pediatric hematology/oncology. 2022. 45. 3. e384-e388
ｍore...
MISC (156)：
Education (2)：
- 2013 - 2017 Gifu University Graduate School of Medicine Department of Pediatrics
- 2000 - 2006 Gifu University School of Medicine Medical Course
Professional career (1)：
Awards (2)：
- 2017/10 - Japanese Society for Inherited Metabolic Diseases Promotion Award Heterozygous carriers of succinyl-CoA:3-oxoacid CoA transferase deficiency can develop severe ketoacidosis
- 2015/11 - Japanese Society for Inherited Metabolic Diseases JCR Travel Award OXCT1 heterozygous carriers could develop severe ketoacidotic episodes in conjunction with ketogenic stresses
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