KANAZAWA Naomi | Department of Inherited Metabolic Disease, National Institute of Neuroscience, NCNP

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著作論文

A novel R275X mutation of the SLC25A15 gene in a Japanese patient with the HHH syndrome
Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis : a common mutation, R179X
An infantile/juvenile form of Alexander disease caused by a R79H mutation in GFAP
A common mutation and a novel mutation in Japanese patients with van der Knaap disease
A case of megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease) : molecular genetic study
Molecular genetic study in Japanese patients with Alexander disease : a novel mutation, R79L
Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis
Distribution of transient receptor potential vanilloid 1(TRPV1)in the trigeminovascular system of the rat
A case of infantile Alexander disease with a milder phenotype and a novel GFAP mutation, L90P
Effects of immunoglobulin therapy in experimental allergic neuritis (EAN) of the Lewis rat induced by P2 myelin protein
T Cell Activation in Demyelinating Neuropathy Associated with "Benign" Anti-Myelin Associated Glycoprotein IgM Gammopathy and in MS : Soluble Interleukin-2 Receptor Levels in Serum and Cerebrospinal Fluid

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