Kira Ryutaro | Department Of Pediatrics Graduate School Of Medical Sciences Kyushu University

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著作論文

A novel R275X mutation of the SLC25A15 gene in a Japanese patient with the HHH syndrome
Mutations of Neuronal Voltage-gated Na^+ Channel α1 Subunit Gene SCN1A in Core Severe Myoclonic Epilepsy in Infancy (SMEI) and in Borderline SMEI (SMEB)
The relationship between retrieval success and task performance during the recognition of meaningless shapes : An event-related near-infrared spectroscopy study
Magnetic resonance studies of brain lesions in patients with Kawasaki disease
Diagnostic usefulness of diffusion-weighted magnetic resonance imaging in influenza-associated acute encephalopathy or encephalitis
Renal Tubular Acidosis Associated With Zonisamide Therapy
Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in Japan
Genetic susceptibility to febrile seizures : Case-control association studies
Clinical study of childhood acute disseminated encephalomyelitis, multiple sclerosis, and acute transverse myelitis in Fukuoka Prefecture, Japan

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