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Classic and non-classic 21-hydroxylase deficiency can be discriminated fromP450 oxidoreductase deficiency in Japanese infants by urinary steroidmetabolites

机译：可以将经典和非经典的21-羟化酶缺乏症与日本婴儿尿类固醇P450氧化还原酶缺乏症代谢物

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期刊名称 Clinical Pediatric Endocrinology
作者
Yuhei Koyama; Keiko Homma; Maki Fukami; Masayuki Miwa; Kazushige Ikeda; Tsutomu Ogata; Mitsuru Murata; Tomonobu Hasegawa;
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作者单位

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年(卷),期 2016(25),2
年度 2016
页码 37–44
总页数 8
原文格式 PDF
正文语种
中图分类儿科学;
关键词
urinary steroid metabolites non-classical 21-hydroxylase deficiency cytochrome P450 oxidoreductase deficiency;

机译：尿类固醇代谢产物;非经典21-羟化酶缺乏症;细胞色素P450氧化还原酶缺乏症;

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1. Classic and non-classic 21-hydroxylase deficiency can be discriminated from P450 oxidoreductase deficiency in Japanese infants by urinary steroid metabolites [J] . Yuhei Koyama, Keiko Homma, Maki Fukami, Clinical Pediatric Endocrinology . 2016,第2期

机译：在日本婴儿中，尿类固醇代谢物可将经典和非经典的21-羟化酶缺乏症与P450氧化还原酶缺乏症区分开
2. 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-hydroxyandrosterone [J] . KoyamaY., HommaK., FukamiM., Clinical Chemistry: Journal of the American Association for Clinical Chemists . 2012,第4期

机译：通过GC-MS测定尿中孕甾烷酮/四氢可的松比率和11β-羟基雄甾酮的两步生化鉴别诊断日本婴儿经典的21-羟化酶缺乏症和细胞色素P450氧化还原酶缺乏症
3. 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-Hydroxyandrosterone [J] . Kazushige Ikeda, Keiko Homma, Maki Fukami, Clinical Chemistry: Journal of the American Association for Clinical Chemists . 2012,第4期

机译：气相色谱-质谱法测定日本婴儿尿中孕甾烷酮/四羟基可的松比例和11β-羟基雄甾烷酮的经典21-羟化酶缺乏症和细胞色素P450氧化还原酶缺乏症的两步生化鉴别诊断。
4. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency A paradigm for prenatal diagnosis and treatment [C] . Saroj Nimkarn, Maria I. New Conference on Skeletal Biology and Medicine . 2010

机译：先天性肾上腺素增生由于21羟化酶缺乏症的产前诊断和治疗范式
5. Vitamin B-12 deficiency in Guatemalan mothers and infants: Prevalence, predictors and associations with maternal depression and infant development. [D] . Jones, Katharine Mary. 2005

机译：危地马拉母亲和婴儿的维生素B-12缺乏症：患病率，预测因素以及与母亲抑郁和婴儿发育的关联。
6. Non-Classic Disorder of Adrenal Steroidogenesis and Clinical Dilemmas in 21-Hydroxylase Deficiency Combined with Backdoor Androgen Pathway. Mini-Review and Case Report [O] . Marta Sumińska, Klaudia Bogusz-Górna, Dominika Wegner, 2020

机译：肾上腺类固醇生成的非经典疾病和21-羟化酶缺乏症与后门雄激素途径结合的临床难题。小型审查和病例报告
7. Screening for Non-classic Steroid 21-Hydroxylase Deficiency in Japanese Women with Infertility and/or Hyperandrogenism [O] . Yosuke Shigematsu, Osamu Nishi, Makoto Kubo, 1994

机译：筛选日本女性的非经典类固醇21-羟化酶缺乏，不孕症和/或高衰弱

Classic and non-classic 21-hydroxylase deficiency can be discriminated fromP450 oxidoreductase deficiency in Japanese infants by urinary steroidmetabolites

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