Asakura, Yumi

Compound heterozygous mutations of cytochrome P450 oxidoreductase gene ( POR ) in two patients with Antley–Bixler syndrome

Adachi, M., Tachibana, K., Asakura, Y., Yamamoto, T., Hanaki, K., & Oka, A. (2004) · American Journal of Medical Genetics Part A

Genomics and Rare DiseasesSexual Differentiation and Disorders

Cited by 110

Mass screening of newborns for congenital hypothyroidism of central origin by free thyroxine measurement of blood samples on filter paper

Adachi, M., Soneda, A., Asakura, Y., Muroya, K., Yamagami, Y., & Hirahara, F. (2012) · European Journal of Endocrinology

Thyroid Disorders and TreatmentsMetabolism and Genetic Disorders

Cited by 56

A Male Patient Presenting with Major Clinical Symptoms of Glucocorticoid Deficiency and Skeletal Dysplasia, showing a Steroid Pattern Compatible with 17.ALPHA.-Hydroxylase/ 17, 20-Lyase Deficiency, but without Obvious CYP 17 Gene Mutations.

ADACHI, M., TACHIBANA, K., ASAKURA, Y., SUWA, S., & NISHIMURA, G. (1999) · Endocrine Journal

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 33

Hypothalamo‐pituitary hypothyroidism detected by neonatal screening for congenital hypothyroidism using measurement of thyroid‐stimulating hormone and thyroxine

Asakura, Y., Tachibana, K., Adachi, M., Suwa, S., & Yamagami, Y. (2002) · Acta Paediatrica

Thyroid Disorders and TreatmentsMetabolism and Genetic Disorders

Cited by 32

The ratio of serum free triiodothyronine to free thyroxine in children: a retrospective database survey of healthy short individuals and patients with severe thyroid hypoplasia or central hypothyroidism

Oto, Y., Muroya, K., Hanakawa, J., Asakura, Y., & Adachi, M. (2015) · Thyroid Research

Thyroid Disorders and TreatmentsGrowth Hormone and Insulin-like Growth Factors

Cited by 16