K. Murayama

Isolated 3-methylcrotonyl-CoA car☐ylase deficiency in a 15-year-old girl

S. Yamaguchi, K. Kodama, T. Shinka, 1997, Brain and Development.

Neurological aspects of del(1q) syndrome.

A. Aylsworth, R. Greenwood, K. Rao, 1991, American journal of medical genetics.

Proteolipid protein gene duplications causing Pelizaeus‐Merzbacher disease: Molecular mechanism and phenotypic manifestations

L. Shaffer, J. Lupski, H. Osaka, 1999, Annals of neurology.

Pelizaeus‐Merzbacher disease: Three novel mutations and implication for locus heterogeneity

I. Kanazawa, K. Fujii, S. Murayama, 1999, Annals of neurology.

Monomelic muscle atrophy

M. Takemitsu, I. Nonaka, M. Kimizuka, 1993, Neuromuscular Disorders.

Developmental Expression of Vasopressin in the Human Hypothalamus: Double-Labeling with In Situ Hybridization and Immunocytochemistry

S. Murayama, R. Meeker, R. Greenwood, 1993, Pediatric Research.

Slowly progressive d-bifunctional protein deficiency with survival to adulthood diagnosed by whole-exome sequencing

T. Matsukawa, S. Tsuji, S. Morishita, 2017, Journal of the Neurological Sciences.

[Effect of intrapulmonary percussive ventilation in a severely disabled patient with persistent pulmonary consolidation].

N. Wada, K. Murayama, E. Kitazumi, 2005, No to hattatsu = Brain and development.