Y. Nishi

Molecular characterization of phenylketonuria in Japanese patients

M. Asada, G. Isshiki, Minoru Asada, 1998, Human Genetics.

Molecular characterization of phenylketonuria and tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiency in Japan

S. Kudo, T. Sakaguchi, Y. Okano, 2011, Journal of Human Genetics.

In Vivo Studies of Phenylalanine Hydroxylase by Phenylalanine Breath Test: Diagnosis of Tetrahydrobiopterin-Responsive Phenylalanine Hydroxylase Deficiency

M. Kajiwara, K. Inui, Yoko Tanaka, 2004, Pediatric Research.

Isolation and purification of an axenic diazotrophic drought-tolerant cyanobacterium, Nostoc commune, from natural cyanobacterial crusts and its utilization for field research on soils polluted with radioisotopes.

K. Tomita-Yokotani, H. Katoh, J. Furukawa, 2012, Biochimica et biophysica acta.

Fabry disease female proband with clinical manifestations similar to hypertrophic cardiomyopathy.

J. Yoshikawa, A. Tanaka, T. Yamano, 2004, Japanese heart journal.

Different attenuated phenotypes of GM2 gangliosidosis variant B in Japanese patients with HEXA mutations at codon 499, and five novel mutations responsible for infantile acute form

L. Hoàng, M. Oka, A. Tanaka, 2003, Journal of Human Genetics.