Thirst perception and arginine vasopressin production in a kindred with an activating mutation of the type 2 vasopressin receptor: The pathophysiology of nephrogenic syndrome of inappropriate antidiuresis

European Journal of Endocrinology

Volumn 161, Issue 3, 2009, Pages 503-508

  Gupta, S ^a   Cheetham, T D ^a,b   Lambert, H J ^a   Roberts, C ^b   Bourn, D ^b   Coulthard, M G ^a   Ball, S G ^b  

^a ROYAL VICTORIA INFIRMARY   (United Kingdom)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ARGININE; ARGIPRESSIN; CYSTEINE; SODIUM; VASOPRESSIN V2 RECEPTOR; VASOPRESSIN RECEPTOR;

ADULT; ARTICLE; CASE REPORT; CHILD; DIURESIS; FEMALE; GENE MUTATION; GENETIC DISORDER; GENETIC SUSCEPTIBILITY; GRAND MAL SEIZURE; HETEROZYGOTE; HUMAN; HYPONATREMIA; INFANT; MALAISE; MALE; NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NEUROENDOCRINE DISEASE; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PRESCHOOL CHILD; PRIORITY JOURNAL; SALT WASTING; SERUM OSMOLALITY; SUPPLEMENTATION; THIRST; TONIC CLONIC SEIZURE; VASOPRESSIN RELEASE; GENETIC PREDISPOSITION; GENETICS; METABOLISM; MUTATION; PERCEPTION; PHYSIOLOGY; SCHWARTZ BARTTER SYNDROME;

ADULT; ARGININE VASOPRESSIN; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; HYPONATREMIA; INAPPROPRIATE ADH SYNDROME; INFANT; MALE; MUTATION; PERCEPTION; RECEPTORS, VASOPRESSIN; THIRST;

EID: 70349251878     PISSN: 08044643     EISSN: 1479683X     Source Type: Journal    
DOI: 10.1530/EJE-09-0246     Document Type: Article

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