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先天性肾上腺皮质增生症的早期观察和护理

Early stage observation and nursing care of patients with congenital adrenal cortical hyperplasia
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作者 金玉梅
出处 《护理研究》 2005年第24期2208-2208,共1页 Chinese Nursing Research
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  • 3Rainey WE,Bird IM,Sawetawan C,et al.Regulation of human adrenal cureinoma cell(NCI-H295)production of C19 steroids.J Clin Endocrinol Metab,1993,77:731.
  • 4Rheaume E,Sanchez R,Simard J,et al.Molecular basis of congenital adrenal hyperplasis in two siblings with classical nonsalt losing 3β-hydroxysteroid dehydrogenase deficiency.J Clinical Endocr and Metab,1994,79:1012.
  • 5Labrie F,Simard J,Luu The V,et al.Structure,function and tissue specific gene expression if 3 hydroxysterpid dehydrogenase 5 one 4 ene isoperase enzymes,in classical and peripheral intracrine steroidogenic tissues.J Steroid Biochem Mol Biol,1992,43:805.
  • 6Fardella CE,Hum DW,Homoki J,et al.Point mutation of arg 440 to his in cytochrome P450 c17 causes severe 17αhydroxylase deficlency.J Clin Endocrinol Metab,1994,79:160.
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  • 8Miller WL,Molecular biology of steroid hormone synthesis.Endocr Rev,1988,9:295.
  • 9Miller WL,Morel Y.The molecular genetics of 21 hydroxylase dificiency.Annu Rev Genet,1989,23:371.
  • 10Speiser PW.Dupont J,Zhu D,et al.Disease expression and molecular genotype in congenital adrenal hyperplasia duo to 21 hydroxylase deficiency.J Clin Inves,1992,90:584.

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