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Meta分析:促肾上腺皮质激素兴奋试验在诊断下丘脑-垂体-肾上腺功能减退中的作用 被引量:3

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摘要 慢性下丘脑-垂体-肾上腺(HPA)功能减退(HPAI)的特点为ACTH分泌减少,可由垂体或下丘脑的病变或损伤,或由长期使用超生理剂量的外源性糖皮质激素引起。
出处 《中华内分泌代谢杂志》 CAS CSCD 北大核心 2009年第2期224-226,共3页 Chinese Journal of Endocrinology and Metabolism
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  • 1陈来照,马景鑑,郑安潮,范益民.128例垂体腺瘤回顾性分析[J].山西医科大学学报,2005,36(4):486-489. 被引量:4
  • 2Yanase T,Simpson ER,Waterman MR.17-Hydroxylase/17,20-lyase deficiency:from clinical investigation to molecular definition.Endocr Rev,1991:91-108. 被引量:1
  • 3Fan YS,Sasi R,Lee C,et al.Localization of the human CYP17 gene[cytochrome P450 (17α)] to 10q24.3 by fluorescence in situ hybridization and simultaneous chromosome banding.Genomics,1992,14:1110-1111. 被引量:1
  • 4Picado-Leonard J,Miller WL.Cloning and sequence of the human 17 gene for P450c17 (steroid 17 alpha-hydroxylase/17,20 lyase):similarity with the gene for P450c21.DNA.1987,6:439-448. 被引量:1
  • 5Winter JS,Couch RM,Muller J,et al.Combined 17α-hydroxylase deficiency and 17,20-desmolase deficiency:evidence for synthesis of a defective cytochrome P450C17.J Clin Endocrinol Metab,1989,68:309-316. 被引量:1
  • 6Biglieri EG,Herron MA,Brust N.17-Hydroxylase deficiency in man.J Clin Invest,1966,45:1946-1960. 被引量:1
  • 7Yang J,Cui B,Sun S,et al.Phenotype-genotype correlation in eight Chinese 17α-hydroxylase/17,20lyase-deficiency patients with five novel mutations of CYP17A1 gene.J Clin Endocrinol Metab,2006,91:3619-3625. 被引量:1
  • 8Wei JQ,Wei JL,Li WC,et al.Genotyping of five chinese patients with 17alpha-hydroxylase deficiency diagnosed through high-performance liquid chromatography serum adrenal profile:identification of two novel CYP17 mutations.J Clin Endocrinol Metab,2006,91:3647-3653. 被引量:1
  • 9Patocs A,Liko I,Varga I,et al.Novel mutation of the CYP17 gene in two unrelated patients with combined 17alpha-hydroxylase/17,20-lyase deficiency:demonstration of absent enzyme activity by expressing the mutant CYP17 gene and by three-dimensional modeling.J Steroid Biochem Mol Biol,2005,97:257-265. 被引量:1
  • 10Wit JM,Jan Roermund HPC,Oostdijk W,et al.Heterozygotes for 17α-hydroxylase deficiency can be detected with a short ACTH test.Clin Endocrinol(Oxf),1988,28:257. 被引量:1

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