THE ENIGMA OF PSEUDOHYPOALDOSTERONISM

被引：13

作者：

CORVOL, P

FUNDER, J

机构：

[1] BAKER MED RES INST, MELBOURNE, VIC 3181, AUSTRALIA

[2] COLL FRANCE, F-75231 PARIS, FRANCE

来源：

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM | 1994年 / 79卷 / 01期

关键词：

D O I：

10.1210/jc.79.1.25

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：25 / 26

页数：2

共 14 条

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[6] TYPE-I PSEUDOHYPOALDOSTERONISM INCLUDES 2 CLINICALLY AND GENETICALLY DISTINCT ENTITIES WITH EITHER RENAL OR MULTIPLE TARGET ORGAN DEFECTS [J].

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[7] POINT MUTATION CAUSING A SINGLE AMINO-ACID SUBSTITUTION IN THE HORMONE BINDING DOMAIN OF THE GLUCOCORTICOID RECEPTOR IN FAMILIAL GLUCOCORTICOID RESISTANCE [J].

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[8]

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[9] PSEUDOHYPOALDOSTERONISM IN 8 FAMILIES - DIFFERENT FORMS OF INHERITANCE ARE EVIDENCE FOR VARIOUS GENETIC-DEFECTS [J].

KUHNLE, U ;

NIELSEN, MD ;

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[10]

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