课题基金 / 基金详情

PHENOTYPE AND GENOTYPE IN CONGENITAL NEPHROGENIC DIABETES INSIPIDUS

PHENOTYPE AND GENOTYPE IN CONGENITAL NEPHROGENIC DIABETES INSIPIDUS
先天性肾性尿崩症的表型和基因型
批准号：
6245151
负责人：
GARY L. ROBERTSON
金额：
$1.2万
依托单位：
NORTHWESTERN UNIVERSITY AT CHICAGO
依托单位国家：
美国
项目类别：
财政年份：
1997
资助国家：
美国
项目状态：
已结题
起止时间：
1997-07-15 至 1997-11-30
来源：
https://reporter.nih.gov/project-details/6245151
关键词：
clinical research congenital kidney disorder genotype human subject nephrogenic diabetes insipidus phenotype vasopressins

项目摘要

项目成果

GARY L. ROBERTSON的其他基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
Congenital nephrogenic diabetes insipidus (CNDI) is an inborn disorder caused by renal insensitivity to the antidiuretic effects of vasopressin. It is characterized clinically by polyuria, polydipsia, and recurrent dehydration which usually manifest themselves within days or weeks of birth. In some cases, the polyuria and polydipsia can be ameliorated. The goal of this project is to determine the relationships between variations in genotype and clinical phenotype in CNDI.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Effect of the Oral Vasopressin Receptor Antagonist CI-1025
PATHOGENESIS AND PATHOPHYSIOLOGY OF FAMILIAL NEUROHYPOPHYSEAL DIABETES
EFFECTS OF VPA 985 AND PLACEBO IN TREATMENT OF HYPONATREMIA
PHENOTYPE AND GENOTYPE IN CONGENITAL NEPHROGENIC DIABETES INSIPIDUS