H. Saijo

Autopsy Findings in Pyruvate Dehydrogenase E1α Deficiency: Case Report

Y. Tokusashi, M. Obata, J. Oki, 1997, Journal of child neurology.

Neuroradiological assessment of visuoperceptual disturbance in children with spina bifida and hydrocephalus

Hajime Tanaka, A. Miyamoto, A. Araki, 1997, Developmental medicine and child neurology.

A case of megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease): molecular genetic study

S. Tsujino, N. Kanazawa, T. Ezoe, 2003, Brain and Development.

Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy.

K. Yokochi, K. Misawa, C. Kim, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Pyruvate dehydrogenase complex deficiency with multiple minor anomalies

J. Oki, Hajime Tanaka, A. Miyamoto, 1997, Acta paediatrica Japonica : Overseas edition.

ASSESSMENT OF VISUOPERCEPTUAL DISTURBANCE IN CHILDREN WITH SPASTIC DIPLEGIA USING MEASUREMENTS OF THE LATERAL VENTRICLES ON CEREBRAL MRI

Hajime Tanaka, A. Miyamoto, A. Araki, 1996, Developmental medicine and child neurology.

The first genetically confirmed Japanese patient with mucolipidosis type IV

N. Matsumoto, H. Saitsu, C. Ohba, 2016, Clinical case reports.

[Thrombocytopenic purpura associated with primary human herpesvirus-6 infection].

M. Saijo, H. Fujiyasu, M. Yamamoto, 1995, Kansenshogaku zasshi. The Journal of the Japanese Association for Infectious Diseases.