Sumitaka Saisho

Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: Newborn screening and its relationship to the diagnosis and treatment of the disorder

Songya Pang, A. Campbell Clark, Eurico Camargo Neto et al. · Screening · 1993 · 161 citations

Medicine, Endocrinology, Pediatrics +16

Genetic Analysis of Japanese Patients with 21-Hydroxylase Deficiency: Identification of a Patient with a New Mutation of a Homozygous Deletion of Adenine at Codon 246 and Patients without Demonstrable Mutations within the Structural Gene for CYP21

Satomi Koyama, Takio Toyoura, Sumitaka Saisho et al. · The Journal of Clinical Endocrinology & Metabolism · 2002 · 37 citations

Life Sciences, Genetics, Molecular Genetics +16

A neonatal mass-screening for congenital adrenal hyperplasia in Japan

Kazuhiko Shimozawa, Sumitaka Saisho, Nobuchika Saito et al. · European Journal of Endocrinology · 1984 · 32 citations

Medicine, Endocrinology, Pediatrics +17

Clinical Course of Patients with Nonclassical 21-hydroxylase Deficiency (21-OHD) Diagnosed in Infancy and Childhood

Kenichi Kashimada, Makoto Ono, Toshikazu Onishi et al. · Endocrine Journal · 2008 · 20 citations · Full text

Medicine, Endocrinology, Pediatrics +17

Age-Related Changes in Serum 17-Hydroxypregnenolone and 17-Hydroxypregnenolone Sulfate Concentrations in Human Infancy and Childhood.

Kazuhiko Shimozawa, Sumitaka Saisho, Junichi Yata et al. · Endocrinologia Japonica · 1988 · 16 citations · Full text

Life Sciences, Endocrinology, Pediatrics +14