NUMURA Yoshiko | Segawa Neurological Clinic for Children
スポンサーリンク
概要
関連著者
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Nomura Yoshiko
Segawa Neurological Clinic For Children
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SEGAWA Masaya
Segawa Neurological Clinic for Children
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NUMURA Yoshiko
Segawa Neurological Clinic for Children
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Nomura Yoshiko
Segawa Neurologic Clinic For Children
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Segawa Masaya
Segawa Neurologic Clinic For Children
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Yamakawa Kazuhiro
Laboratory of Neurogenetics, RIKEN, Brain Science Institute
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Yamakawa Kazuhiro
Laboratory For Neurogenetics Riken Brain Science Institute
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Yamakawa Kazuhiro
Laboratory For Neurogenetics Brain Science Institute Institute Of Physical And Chemical Research (ri
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Yamakawa Kazuhiro
Department Of Otolaryngology Kochi Medical School
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Nomura Yoshiko
瀬川小児神経学クリニック
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KIMURA Kazue
Segawa Neurological Clinic for Children
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HOSHINO Kyoko
Segawa Neurological Clinic for Children
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HACHIMORI Kei
Segawa Neurological Clinic for Children
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Amano Kenji
Laboratory For Neurogenetics Brain Science Institute The Institute Of Physical And Chemical Research
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SUGAWARA Takashi
Laboratory of Food and Biomolecular Science, Graduate School of Agricultural Science, Tohoku Univers
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Mazaki-miyazaki Emi
Laboratory For Neurogenetics Riken Brain Science Institute
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TATENO Akihiko
Department of Pediatrics, Toho University School of Medicine, Sakura Hospital
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Suzuki Michiyo
Segawa Neurological Clinic For Children
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Tateno Akihiko
Department Of Pediatrics Toho University Medical Center Sakura Hospital
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Tateno Akihiko
Department Of Pediatrics Toho University School Of Medicine Sakura Hospital
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UCHINO June
Segawa Neurological Clinic for Children
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SAGAWA Masaya
Segawa Neurological Clinic for Children
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Sugawara Takashi
Laboratory For Neurogenetics Riken Brain Science Institute
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NAGAO Yuri
Segawa Neurological Clinic for Children
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Tateno Akihiko
Department Of Pediatrics Sakura Hospital Toho University School Of Medicine
著作論文
- A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures
- R133C and R168X mutations in Japanese Rett syndrome patients : a caution for misdiagnosis
- Mutational analysis of the MECP2 gene in Japanese patients with Rett syndrome
- Development of language in Rett syndrome
- Epilepsy in autism : A pathophysiological consideration