T. Honma

Fluctuation of Computed Tomographic Findings in White Matter in Alexander's Disease

T. Shiihara, Mitsuhiro Kato, K. Hayasaka, 2002, Journal of child neurology.

Sonic hedgehog signal peptide mutation in a patient with holoprosencephaly

T. Shiihara, E. Nanba, Mitsuhiro Kato, 2000, Annals of neurology.

Diffuse pachygyria with cerebellar hypoplasia: A milder form of microlissencephaly or a new genetic syndrome?

Mitsuhiro Kato, A. Ito, K. Hayasaka, 1999, Annals of neurology.

Progressive Sliding Hiatal Hernia as a Complication of Menkes' Syndrome

T. Shiihara, Mitsuhiro Kato, H. Kodama, 2002, Journal of Child Neurology.

Spondyloepimetaphyseal dysplasia with joint laxity leptodactylic form: Clinical course and phenotypic variations in four patients

Y. Fukushima, T. Shiihara, S. Ikegawa, 2002, American journal of medical genetics. Part A.

Compound heterozygous PMP22 deletion mutations causing severe Charcot–Marie–Tooth disease type 1

Mitsuhiro Kato, Kazuyuki Nakamura, Chizuru Seiwa, 2010, Journal of Human Genetics.