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3. An autopsy case of sporadic amyotrophic lateral sclerosis associated with the I113T SOD1 mutation. Issue 1 (17th June 2013)

5. ATP13A2 deficiency induces a decrease in cathepsin D activity, fingerprint‐like inclusion body formation, and selective degeneration of dopaminergic neurons. Issue 9 (13th March 2013)

7. Clinical similarities of hereditary progressive/dopa responsive dystonia caused by different types of mutations in the GTP cyclohydrolase I gene. Issue 4 (1st April 1998)

8. Clinicopathologic features of autosomal recessive amyotrophic lateral sclerosis associated with optineurin mutation. Issue 1 (29th July 2013)

9. Contrast enrichment of spinal cord MR imaging using a ratio of T1‐weighted and T2‐weighted signals. Issue 5 (4th November 2013)