H. Tomi

发表

Middle latency auditory-evoked potentials in myotonic dystrophy: relation to the size of the CTG trinucleotide repeat and intelligent quotient

S. Tobimatsu, K. Arakawa, J. Kira, 2003, Journal of the Neurological Sciences.

Involvement of the spinal posterior horn in Gerstmann–Sträussler–Scheinker disease (PrP P102L)

E. Otomo, Y. Itoh, H. Mizusawa, 1999, Neurology.

Hereditary distal dominant amyotrophy followed by spastic paraplegia.

H. Tomi, N. Sunohara, M. Mukoyama, 1993, Internal medicine.

Carotid gustatory syndrome in a patient with Holmes-Adie syndrome.

H. Shibasaki, H. Tomi, 1990, Journal of neurology, neurosurgery, and psychiatry.

Myopathy, Unique Clinical Features, and Brain Malformations Mimicking Fukuyama Congenital Muscular Dystrophy: A Case Report

I. Nonaka, H. Nakayama, K. Eto, 1993 .

Myotonia congenita with painful muscle cramps.

I. Nonaka, K. Arahata, H. Tomi, 1996, Internal medicine.

[A case of autoimmune polyglandular deficiency associated with progressive myopathy].

I. Nonaka, H. Tomi, N. Sunohara, 1992, Rinsho shinkeigaku = Clinical neurology.

Supranuclear paralysis preventing lid closure in amyotrophic lateral sclerosis.

H. Tomi, N. Sunohara, M. Mukoyama, 1989, Japanese journal of medicine.

Complicated hereditary spastic paraplegia with peripheral neuropathy, optic atrophy and mental retardation.

S. Kimiya, K. Arimoto, H. Tomi, 2000, Neuropediatrics.

Glabella tap sign Is it due to a lack of R2-habituation?

H. Tomi, N. Sunohara, E. Satoyoshi, 1985, Journal of the Neurological Sciences.