Nephrogenic syndrome of inappropriate antidiuresis (NSIAD): A paradigm for activating mutations causing endocrine dysfunction

Pediatric Endocrinology Reviews

Volumn 4, Issue SUPPL. 1, 2006, Pages 66-70

  Rosenthal, Stephen M ^a,b   Feldman, Brian J ^a   Vargas, Gabriel A ^a   Gitelman, Stephen E ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Constitutive activation; G protein coupled receptor mutations; Nephrogenic syndrome of inappropriate antidiuresis (NSIAD); V2 vasopressin receptor

Indexed keywords

ARGIPRESSIN; ARGIPRESSIN RECEPTOR; DEMECLOCYCLINE; G PROTEIN COUPLED RECEPTOR; LITHIUM; RECEPTOR BLOCKING AGENT; UREA; VASOPRESSIN; VASOPRESSIN ANTAGONIST; VASOPRESSIN V2 RECEPTOR;

ARTICLE; FLUID BALANCE; GENE MUTATION; HOMEOSTASIS; HORMONE ACTION; HORMONE RELEASE; HUMAN; INAPPROPRIATE VASOPRESSIN SECRETION; INCIDENCE; MISSENSE MUTATION; NEPHROGENIC DIABETES INSIPIDUS; NONHUMAN; PLASMA OSMOLALITY; PROTEIN FUNCTION; PROTEIN STRUCTURE; URINE OSMOLALITY; WATER DEPRIVATION;

BODY WATER; DIABETES INSIPIDUS, NEPHROGENIC; HOMEOSTASIS; HUMANS; INAPPROPRIATE ADH SYNDROME; INFANT; MUTATION; RECEPTORS, VASOPRESSIN;

EID: 33846862458     PISSN: 15654753     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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