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Human Reproduction (Oxford, England)|August 31, 2020
Foetal virilisation caused by overproduction of non-aromatisable 11-oxygenated C19 steroids in maternal adrenal tumourKeisuke Nagasaki, Kaoru Takase, Chikahiko Numakura, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 3, 2014
A Case of a Preterm Infant with 21-Hydroxylase Deficiency: Implications of the Biochemical Diagnosis with Urinary Pregnanetriolone by Gas Chromatography/Mass Spectrometry in Selected Ion Monitoring (GCMS-SIM)Takashi Hamajima, Shigeru Ohki, Hiroki Imamine, et al.
Hormone Research in Paediatrics|May 14, 2014
Discordant genotype-phenotype correlation in familial hyperaldosteronism type III with KCNJ5 gene mutation: a patient report and review of the literatureMasanori Adachi, Koji Muroya, Yumi Asakura, et al.
Endocrine Journal|June 11, 2019
Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiencyGoro Sasaki, Tomohiro Ishii, Naoaki Hori, et al.
Pediatric Research|January 28, 2006
Cytochrome P450 oxidoreductase deficiency in three patients initially regarded as having 21-hydroxylase deficiency and/or aromatase deficiency: diagnostic value of urine steroid hormone analysisMaki Fukami, Tomonobu Hasegawa, Reiko Horikawa, et al.
Neurochemistry International|March 17, 2007
Upregulation of IGF-I in the goldfish retinal ganglion cells during the early stage of optic nerve regenerationYoshiki Koriyama, Keiko Homma, Kayo Sugitani, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 19, 2006
Specificity assessment of immunoassay kits for determination of urinary free cortisol concentrationsHitoshi Horie, Takeshi Kidowaki, Yuhei Koyama, et al.
Internal Medicine (Tokyo, Japan)|November 18, 2016
Feminizing Adrenocortical Carcinoma with Distinct Histopathological FindingsMasako Hatano, Yasuhiro Takenaka, Ikuo Inoue, et al.
Clinical Chemistry|January 26, 2012
Two-step biochemical differential diagnosis of classic 21-hydroxylase deficiency and cytochrome P450 oxidoreductase deficiency in Japanese infants by GC-MS measurement of urinary pregnanetriolone/ tetrahydroxycortisone ratio and 11β-hydroxyandrosteroneYuhei Koyama, Keiko Homma, Maki Fukami, et al.
Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|May 24, 2016
Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolitesYuhei Koyama, Keiko Homma, Maki Fukami, et al.
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