Suwa, S

Worldwide Experience in Newborn Screening for Classical Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Pang, S., Wallace, M. A., Hofman, L., Thuline, H. C., Dorche, C., Lyon, I. C. T., Dobbins, R. H., Kling, S., Fujieda, K., & Suwa, S. (1988) · Journal of Urology

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 392

Spontaneous puberty in 46,XX subjects with congenital lipoid adrenal hyperplasia. Ovarian steroidogenesis is spared to some extent despite inactivating mutations in the steroidogenic acute regulatory protein (StAR) gene.

Fujieda, K., Tajima, T., Nakae, J., Sageshima, S., Tachibana, K., Suwa, S., Sugawara, T., & Strauss, J. F. (1997) · Journal of Clinical Investigation

Sexual Differentiation and DisordersAdrenal Hormones and Disorders

Cited by 162

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