K. Maeda

Prenatal Diagnosis and Neonatal Monitoring of a Fetus with Glutaric Aciduria Type II Due to Electron Transfer Flavoprotein (β-Subunit) Deficiency

T. Hashimoto, S. Previs, P. Rinaldo, 1991, Pediatric Research.

N‐Acetyltransferase Activity in the Urine in Japanese Subjects: Comparison in Healthy Persons and Bladder Cancer Patients

T. Hanaoka, Y. Ohishi, K. Maeda, 1995, Japanese journal of cancer research : Gann.

A new variant of glutaric aciduria type II: Deficiency of β-subunit of electron transfer flavoprotein

T. Hashimoto, M. Oshima, S. Yamaguchi, 1990, Journal of Inherited Metabolic Disease.

Newly Identified Forms of Electron Transfer Flavoprotein Deficiency in Two Patients with Glutaric Aciduria Type II

T. Hashimoto, Yasuyuki Suzuki, M. Oshima, 1991, Pediatric Research.

Arima syndrome caused by CEP290 specific variant and accompanied with pathological cilium; clinical comparison with Joubert syndrome and its related diseases

M. Itoh, Takashi Saito, K. Narita, 2017, Brain and Development.

Improvement of clinical and MM findings in a boy with adrenoleukodystrophy by dietary erucic acid therapy

H. Moser, Yasuyuki Suzuki, T. Orii, 1992, Brain and Development.