O. Ueda

Permanent Neonatal Diabetes Mellitus with Growth Disturbance, Developmental Delay, Epilepsy and Dysmorphic Features

Yoshiya Ito, K. Fujieda, T. Mukai, 2005 .

Familial paralysis agitans juvenilis; a clinical, anatomical and genetic study.

O. Ueda, Y. Ota, S. Miyoshi, 1958, Folia psychiatrica et neurologica japonica.

Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia.

Y. Kikuchi, K. Tomita, H. Nonoguchi, 2005, The Journal of clinical endocrinology and metabolism.

Molecular basis of neonatal diabetes in Japanese patients.

Y. Makita, K. Fujieda, T. Mukai, 2007, The Journal of clinical endocrinology and metabolism.

FAMILTAL PARALYSIS AGITANS JUVENILIS. A CLINICAL, ANATOMICAL AND GENETIC STUDY

O. Ueda, Y. Ota, S. Miyoshi, 1958 .

A 34-year-old Japanese patient exhibiting NBAS deficiency with a novel mutation and extended phenotypic variation.

K. Fujieda, H. Azuma, Tsunehisa Nagamori, 2020, European journal of medical genetics.