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Neonatal screening for congenital adrenal hyperplasia in Japan.

作者信息

Naruse H, Suzuki E, Irie M, Tsuji A, Takasugi N, Fukushi M, Matsuura N, Shimozawa K

出版信息

Ann N Y Acad Sci. 1985;458:103-10. doi: 10.1111/j.1749-6632.1985.tb14596.x.

DOI:10.1111/j.1749-6632.1985.tb14596.x
PMID:3911846
Abstract
摘要

相似文献

1
Neonatal screening for congenital adrenal hyperplasia in Japan.日本先天性肾上腺皮质增生症的新生儿筛查
Ann N Y Acad Sci. 1985;458:103-10. doi: 10.1111/j.1749-6632.1985.tb14596.x.
2
Neonatal screening program for congenital adrenal hyperplasia in a homogeneous Caucasian population.
Ann N Y Acad Sci. 1985;458:85-9. doi: 10.1111/j.1749-6632.1985.tb14594.x.
3
[Neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 1. Enzyme immunoassay of dried blood 17 alpha-hydroxyprogesterone and its application to neonatal screening for congenital adrenal hyperplasia].[21-羟化酶缺乏所致先天性肾上腺皮质增生症的新生儿筛查。1. 干血17α-羟孕酮的酶免疫测定及其在先天性肾上腺皮质增生症新生儿筛查中的应用]
Nihon Naibunpi Gakkai Zasshi. 1986 Jun 20;62(6):683-96. doi: 10.1507/endocrine1927.62.6_683.
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Newborn screening for congenital adrenal hyperplasia with special reference to screening in Alaska.先天性肾上腺增生症的新生儿筛查，特别提及阿拉斯加的筛查情况。
Ann N Y Acad Sci. 1985;458:90-102. doi: 10.1111/j.1749-6632.1985.tb14595.x.
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[Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].[21-羟化酶缺乏所致肾上腺增生：产前诊断与治疗。新生儿诊断]
Rev Med Liege. 1986 Jan 15;41(2):37-44.
6
[Neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 2. Analysis of steroids with high-performance liquid chromatography for diagnosis of congenital adrenal hyperplasia].
Nihon Naibunpi Gakkai Zasshi. 1987 Feb 20;63(2):102-12. doi: 10.1507/endocrine1927.63.2_102.
7
[Neonatal screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. 3. An enzyme-linked immunosorbent assay for dried blood 17 alpha-hydroxyprogesterone].[新生儿21-羟化酶缺乏所致先天性肾上腺皮质增生症的筛查。3. 干血17α-羟孕酮的酶联免疫吸附测定法]
Nihon Naibunpi Gakkai Zasshi. 1987 Feb 20;63(2):113-22.
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Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.全球范围内针对因21-羟化酶缺乏所致经典型先天性肾上腺皮质增生症的新生儿筛查经验。
Pediatrics. 1988 Jun;81(6):866-74.
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Prevalence of adrenal 21-hydroxylase deficiency in neonates born in the West Midlands: a retrospective study.
J Inherit Metab Dis. 1986;9 Suppl 1:155-6. doi: 10.1007/BF01800871.
10
[Neonatal mass-screening for congenital adrenal hyperplasia due to 21-hydroxylase deficiency. II. A pilot neonatal mass-screening study in the west of Shizuoka Prefecture, Japan].[21-羟化酶缺乏所致先天性肾上腺皮质增生症的新生儿群体筛查。II. 日本静冈县西部的一项新生儿群体筛查试点研究]
Nihon Naibunpi Gakkai Zasshi. 1983 Dec 20;59(12):1860-73. doi: 10.1507/endocrine1927.59.12_1860.

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In Vitro Enzyme Assay of CYP21A2 Mutation (R483Q) by A Novel Method Using Liquid Chromatography-Electrospray Ionization Tandem Mass Spectrometry (LC-ESI-MS/MS).采用液相色谱 - 电喷雾电离串联质谱法（LC - ESI - MS/MS）的新方法对CYP21A2突变（R483Q）进行体外酶分析
Clin Pediatr Endocrinol. 2008;17(2):49-56. doi: 10.1297/cpe.17.49. Epub 2008 May 8.
2
Influence of spironolactone on neonatal screening for congenital adrenal hyperplasia.螺内酯对先天性肾上腺皮质增生症新生儿筛查的影响。
Arch Dis Child Fetal Neonatal Ed. 1999 Nov;81(3):F179-83. doi: 10.1136/fn.81.3.f179.
3
Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.
基因转换样事件导致先天性肾上腺皮质增生症中的类固醇21-羟化酶缺乏。
Proc Natl Acad Sci U S A. 1987 Nov;84(22):8091-4. doi: 10.1073/pnas.84.22.8091.