期刊文献+

遗传性垂体性尿崩症一个家系分析 被引量:3

原文传递
导出
摘要 遗传性垂体性尿崩症一个家系分析陈育才谢文煌谢卉陈智辉陈聪水遗传性垂体性尿崩症的遗传方式有二种,常染色体显性或伴性遗传。常染色体显性遗传垂体性尿崩症(ADNDI)临床上罕见。我们发现一个家系,报告如下。一、临床资料1.家系调查:该家系(附图)四代17人...
出处 《中华内分泌代谢杂志》 CAS CSCD 北大核心 1997年第4期253-253,共1页 Chinese Journal of Endocrinology and Metabolism
  • 相关文献

同被引文献15

  • 1孙洪涛,叶蕾,王卫庆,姜蕾,苏颋为,刘建民,陈瑛,李小英,宁光.Glu^(47)缺失造成的常染色体显性遗传垂体性尿崩症的家系分析[J].中华内分泌代谢杂志,2005,21(5):435-437. 被引量:3
  • 2陈育才.垂体性尿崩症的分子遗传学进展[J].国外医学(内分泌学分册),1996,16(2):85-86. 被引量:2
  • 3Kawasaki E,Diabetes,1998年,47卷,733页
  • 4Roberts J Ⅱ, Anthony LB. In: Wilson JD, et al (eds). Williams Textbook of Endocrinology. 9th ed. Philadlphia: W, B. Saunders Co,1998,362-363.
  • 5Repaske DR, Phillips JA 3rd, Kirby LT. Molecular analysis of autosomal dominant neurohypophyseal diabetes insipidus. J Clin Endecrinol Metab, 1990,70:752-757.
  • 6Christensen JH, Siggaard C, Corydon TJ. Impaired trafficking of mutated AVP prohormone in cells expressing tare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus. Clin Endocrinol (Oxf), 2004,60:125-136.
  • 7Gabreels BA, Swaab DF, de kleijn DP, et al. Attenuation of the polypeptide 7B2, prohormone convertase PC2, and vasopressin in the hypothalamus of some Prader-Willi patients : indications for a processing defect. J Clin Endecrinol Metab, 1998,83:591-599.
  • 8Rossi NF. Regulation of vasopressin secretion by ETA and ETB receptors in compartmentalized rat hypothalamo-neurohypophysial Explants. Am J Physiol Endocrinol Metab, 2004,286 : ES35-E541.
  • 9Ishizaki S, Murase T, Sugimura Y. Role of ghrelin in the regulation of vasopressin release in conscious rats. Endocrinology, 2002,143:1589-1593.
  • 10Kuwahara S, Arima H, Banno R. Regulation of vasopressin gene expression by cAMP and glucocorticoids in parvocellular neurons of the paraventricular nucleus in rat hypothalamic organotypic cultures. J Neurosci, 2003,23 : 10231-10237.

引证文献3

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部