Pseudohypoaldosteronism: Family studies to identify asymptomatic carriers by stimulation of the renin-aldosterone system

Hormone Research in Paediatrics

Volumn 46, Issue 3, 1996, Pages 124-129

  Kuhnle, Ursula ^a   Hinkei, G K ^b   Hubl, W ^c   Reichelt, T ^b  

^a LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^b DRESDEN UNIVERSITY OF TECHNOLOGY   (Germany)

^c ACADEMIC TEACHING HOSPITAL DRESDEN FRIEDRICHSTADT   (Germany)

Author keywords

Biochemical variability; Familial pseudohypoaldosteronism; Pattern of inheritance

Indexed keywords

ALDOSTERONE; ALDOSTERONE RECEPTOR; FUROSEMIDE; RENIN; SODIUM;

ADOLESCENT; ADULT; ALDOSTERONE BLOOD LEVEL; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; FAMILIAL DISEASE; FAMILY STUDY; FEMALE; HETEROZYGOTE DETECTION; HUMAN; MALE; MONOCYTE; NORMAL HUMAN; PEDIGREE; PLASMA RENIN ACTIVITY; PRIORITY JOURNAL; PSEUDOHYPOALDOSTERONISM; RECEPTOR BINDING; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; SODIUM BLOOD LEVEL; SODIUM DEPLETION;

EID: 0029780458     PISSN: 16632818     EISSN: 16632826     Source Type: Journal    
DOI: 10.1159/000185008     Document Type: Article

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