T. Oohira

The infantile form of sialidosis type II associated with congenital adrenal hyperplasia: Possible linkage between HLA and the neuraminidase deficiency gene

I. Akaboshi, I. Matsuda, S. Naito, 1985, Human Genetics.

The patient with combined deficiency of neuraminidase and 21-hydroxylase

T. Sasazuki, Y. Nishimura, I. Matsuda, 1987, Human Genetics.

Clinical and molecular analysis of a Japanese boy with Morquio B disease

F. Endo, I. Matsuda, A. Oshima, 1995, Clinical genetics.

Usefulness of adhesive strapping for umbilical hernias of infants

T. Moroi, T. Kuwahara, Akito Kitano, 2020, Pediatrics international : official journal of the Japan Pediatric Society.