Yamamoto Akiyo | 神戸大学医学系研究科
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概要
関連著者
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YOKOYAMA Naoki
Fujitsu Laboratories Ltd.
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Yokoyama Naoki
Department of Pediatrics, Kobe University Graduate School of Medicine
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Nakamura Hajime
Hyogo Prefectural Kobe Children's Hospital
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Yokoyama N
Fujitsu Laboratories Ltd.
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Nakamura H
Hyogo Prefectural Kobe Children's Hospital
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Yamamoto Akiyo
神戸大学医学系研究科
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Uetani Yoshiyuki
神戸大学医学系研究科
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Yonetani M
Kobe Univ. Graduate School Of Medicine Kobe Jpn
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Yokoyama Naoki
Institute For Nano Quantum Information Electronics The University Of Tokyo
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Nakamura Hajime
Department Of Development And Aging Faculty Of Medicine Kobe University Graduate School Of Medicine
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NAKAMURA Hajime
Division of Cardiology, Department of Internal Medicine, Kinki University School of Medicine
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Nishio Hisahide
神戸大学医学系研究科
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Nakamura Hajime
神戸大学医学部
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Nakamura Hajime
Division Of Cardiology Department Of Internal Medicine Kinki University School Of Medicine
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Nishio Hisahide
Department Of Genetic Epidemiology Graduate School Of Medicine Kobe University
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Nishio Hisahide
Department Of Pubic Health And Genetic Epidemiology Kobe University Graduate School Of Medicine
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Nakao Hideto
Department Of Neonatology Hyogo Children's Hospital Perinatal Center
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Yamamoto Akiyo
Division Of Applied Biosciences Graduate School Of Agriculture Kyoto University
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YOKOYAMA NAOKI
Division of Pediatrics, Department of Development and Aging, Faculty of Medicine, Kobe University Gr
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YONETANI MASAHIKO
Division of Pediatrics, Department of Development and Aging, Faculty of Medicine, Kobe University Gr
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UETANI YOSHIYUKI
Division of Pediatrics, Department of Development and Aging, Faculty of Medicine, Kobe University Gr
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NAKAO HIDETO
Kobe Children's Hospital Perinatal Center
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Waku Shozo
神戸大学医学系研究科
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Yokoyama Naoki
神戸大学医学系研究科
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Yonetani Masahiko
神戸大学医学系研究科
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Nishio H
Department Of Public Health Kobe University Graduate School Of Medicine
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Nakamura Hajime
神戸大学医学系研究科
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NAKAO HIDETO
Kobe Children's Hospital Perinatal Center
著作論文
- Evaluation of change of cerebral circulation by SpO_2 in preterm infants with apneic episodes using near infrared spectroscopy
- Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population