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Neurology|August 23, 2000
Variability and validity of polymorphism association studies in Parkinson's diseaseE K Tan, M Khajavi, J I Thornby, et al.Neurology|December 13, 2000
A "dystrophic" variant of autosomal recessive myotonia congenita caused by novel mutations in the CLCN1 geneS Nagamitsu, T Matsuura, M Khajavi, et al.Neuroscience Letters|May 18, 2001
Alcohol dehydrogenase polymorphism and Parkinson's diseaseE K Tan, S Nagamitsu, T Matsuura, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 1999
Decreased cerebellar blood flow in postinfectious acute cerebellar ataxiaS Nagamitsu, T Matsuishi, M Ishibashi, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|May 20, 1998
Age-related changes in the cerebrospinal fluid level of beta-endorphin and substance P. Short communicationS Nagamitsu, T Matsuishi, H Komori, et al.Internal Medicine (Tokyo, Japan)|March 1, 1994
Neuroimaging and neuropathologic findings in AIDS patient with cytomegalovirus infectionS Nagamitsu, S Okabayashi, S Dai, et al.Brain & Development|July 14, 1998
Baló's concentric sclerosis in a 4-year-old Japanese infantY Murakami, T Matsuishi, T Shimizu, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|May 9, 2001
Decreased cerebrospinal fluid levels of beta-endorphin and ACTH in children with infantile spasmsS Nagamitsu, T Matsuishi, Y Yamashita, et al.Journal of Autism and Developmental Disorders|April 1, 1997
CSF beta-endorphin levels in patients with infantile autismS Nagamitsu, T Matsuishi, T Kisa, et al.Internal Medicine (Tokyo, Japan)|May 1, 1997
Facioscapulohumeral muscular dystrophy: clinical diversity and genetic abnormalities in Japanese patientsM Nakagawa, T Matsuzaki, I Higuchi, et al.Pageof 4