Takio Toyoura

Molecular Basis of Nonclassical Steroid 21-Hydroxylase Deficiency Detected by Neonatal Mass Screening in Japan

Toshihiro Tajima, KENJI FUJIEDA Jun Nakae, Takio Toyoura et al. · The Journal of Clinical Endocrinology & Metabolism · 1997 · 43 citations

Medicine, Endocrinology, Pediatrics +17

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

Elevated Urine Pregnanetriolone Definitively Establishes the Diagnosis of Classical 21-Hydroxylase Deficiency in Term and Preterm Neonates

Keiko Homma, Tomonobu Hasegawa, Eiko Takeshita et al. · The Journal of Clinical Endocrinology & Metabolism · 2004 · 37 citations · Full text

Medicine, Endocrinology, Pediatrics +16

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

An XX Male With Microphthalmos and Sclerocornea

Miwako Kobayashi, Motohiro Kiyosawa, Takio Toyoura et al. · Journal of Pediatric Ophthalmology & Strabismus · 1998 · 17 citations

Life Sciences, Genetics, Ophthalmology +15