Kishikawa Yumiko | Department Of Pediatrics Yamagata University School Of Medicine
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概要
関連著者
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Hayasaka Kiyoshi
Department Of Pediatrics Yamagata University Faculty Of Medicine
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Kishikawa Yumiko
Department Of Pediatrics Yamagata University School Of Medicine
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KISHIKAWA Yumiko
Department of Pediatrics, Yamagata University School of Medicine
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ABE AKIKO
Department of Gerodontology, School of Dentistry, Aichi Gakuin University
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Hayasaka K
Department Of Pediatrics Yamagata University School Of Medicine
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NUMAKURA CHIKAHIKO
Department of Pediatrics, Yamagata University School of Medicine
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Numakura C
Department Of Pediatrics Yamagata University School Of Medicine
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Numakura Chikahiko
Department Of Pediatrics Yamagata University School Of Medicine
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Hayashi Makiko
Department Of Chemistry Faculty Of Science Fukuoka University
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ABE Akiko
Department of Pediatrics, Yamagata University School of Medicine
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Abe Akiko
Department Of Pediatrics Yamagata University School Of Medicine
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ABE Akiko
Department of Obstetrics and Gynecology, The University of Tokushima, School of Medicine
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Sasaki Ayako
山形大学 医学部小児科学
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Sasaki Ayako
Department Of Pediatrics Yamagata University School Of Medicine
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Otagiri Tesshu
山形大学 医学部小児科学
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HAYASAKA KIYOSHI
Department of Pediatrics, Yamagata University School of Medicine
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Hayasaka Kiyoshi
Department Of Pediatrics Yamagata University School Of Medicine
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Hayasaka Kiyoshi
Departments Of Pediatrics Yamagata University School Of Medicine
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Sasaki Ayako
Department Of Biofunctional Science Faculty Of Agriculture And Life Science Hirosaki University
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OTAGIRI Tesshu
Department of Pediatrics, Yamagata University School of Medicine
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Meguro Toru
Department Of Pathology Yamagata University School Of Medicine
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Shirahata Emi
Department Of Pediatrics Yamagata University School Of Medicine
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Shirahata Emi
Department Of Pediatrics Yamagata City Hospital Saiseikan
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Otagiri Tesshu
Department Of Pediatrics Yamagata University School Of Medicine
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Saito Kayoko
Institute Of Medical Genetics
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Watanabe Kyoko
Department Of Basic Space Science Japan Aerospace Exploration Agency
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Murakami Tatsufumi
Department Of Neurology Kumamoto University School Of Medicine
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Chida Keiji
Department Of Clinical Neurology National Iwate Hospital
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Oka Nobuyuki
Department Of Internal Medicine Shimane Medical University
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Mochizuki Narutaka
Department Of Pediatrics Sakai Municipal Hospital
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Nakamura Kazuyuki
Department Of Biochemistry And Biomolecular Recognition Yamaguchi University School Of Medicine
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Kato Mitsuhiro
Department Of Applied Chemistry Aichi Institute Of Technology
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Yoshida Yuki
Department Of Bioscience Tokyo University Of Agriculture
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Iai Mizue
Division Of Neurology Kanagawa Children's Medical Center
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Toyota Kentaro
Department Of Pediatrics Yamagata University School Of Medicine
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Koide Hiroyoshi
Hallo Clinic
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OKA Nobuyuki
NHO Minami-Kyoto Hospital
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HONMA Akira
Honma Child Clinic
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Seiwa Chizuru
Department Of Pediatrics Yamagata Medical Rehabilitation Center For Disabled Persons
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Meguro Toru
Department Of Pediatrics Yamagata University School Of Medicine
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Hayashi Makiko
Yamagata Univ. School Of Medicine Yamagata Jpn
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Mochizuki Narutaka
Department Of Neonatal Medicine Osaka Medical Center And Research Institute For Maternal And Child Health
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HONMA Tomomi
Department of Pediatrics, Yamagata Prefectural Shinjo Hospital
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ITOH Aiko
Department of Pediatrics, Yamagata Medical Rehabilitation Center for Disabled Persons
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Honma Tomomi
Department Of Pediatrics Yamagata Prefectural Shinjo Hospital
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Itoh Aiko
Department Of Pediatrics Yamagata Medical Rehabilitation Center For Disabled Persons
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Nakamura Kazuyuki
Department Of Pediatrics Yamagata University School Of Medicine
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Yoshida Yuki
Department of Pediatrics, Yamagata University School of Medicine
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ARAI Hidee
Department of Neurology, Chiba Children's Hospital
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Hayashi Makiko
Department of Pediatrics, Yamagata University School of Medicine
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YAMAO Satoshi
Department of Neurology, Kurashiki Riverside Hospital
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HATTORI Hideji
Nishinomiya-Sunago Medical and Welfare Center
著作論文
- Inheritance of polyalanine expansion mutation of PHOX2B in congenital central hypoventilation syndrome
- Neurofilament light chain polypeptide gene mutations in Charcot-Marie-Tooth disease : nonsense mutation probably causes a recessive phenotype
- Compound heterozygous PMP22 deletion mutations causing severe Charcot-Marie-Tooth disease type 1
- Molecular analysis of the genes causing recessive demyelinating Charcot-Marie-Tooth disease in Japan