Familial nephrogenic syndrome of inappropriate antidiuresis: Dissociation between aquaporin-2 and vasopressin excretion

Journal of Clinical Endocrinology and Metabolism

Volumn 95, Issue 9, 2010, Pages

  Ranchin, Bruno ^a   Boury Jamot, Mathieu ^f,g   Blanchard, Gaëlle ^a   Dubourg, Laurence ^a,b,d   Hadj Aïssa, Aoumeur ^b,d   Morin, Denis ^h   Durroux, Thierry ^h   Cochat, Pierre ^a,e   Bricca, Giampiero ^b,c   Verbavatz, Jean Marc ^f,g   Geelen, Ghislaine ^c,d  

^a HOSPICES CIVILS DE LYON   (France)

^b INSERM   (France)

^c CROIX ROUSSE HOSPITAL   (France)

^d Lab de Physiologie de l'Exercice   (France)

^e UNIVERSITÉ LYON 1   (France)

^f CNRS   (France)

^g UNIVERSITÉ PARIS SACLAY   (France)

^h MONTPELLIER UNIVERSITY HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AQUAPORIN 2; VASOPRESSIN; VASOPRESSIN V2 RECEPTOR; VASOPRESSIN DERIVATIVE; VASOPRESSIN RECEPTOR;

ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DILUTION; DISEASE SEVERITY; FAMILIAL DISEASE; FAMILY ASSESSMENT; FEMALE; GENE MUTATION; GENETIC VARIABILITY; HEMIZYGOSITY; HETEROZYGOTE; HUMAN; HYPONATREMIA; INAPPROPRIATE VASOPRESSIN SECRETION; INTENSIVE CARE UNIT; KIDNEY CONCENTRATING CAPACITY; MALE; MENTAL DEFICIENCY; MOTHER; NEPHROGENIC SYNDROME OF INAPPROPRIATE ANTIDIURESIS; NEUROHYPOPHYSIS DISEASE; PATHOPHYSIOLOGY; PEDIGREE ANALYSIS; PHENOTYPE; PRIORITY JOURNAL; RECURRENT DISEASE; SEIZURE; URINALYSIS; URINARY EXCRETION; URINE OSMOLALITY; WATER LOADING; CASE CONTROL STUDY; CASE REPORT; FAMILY; GENETICS; INFANT; METABOLISM; NUCLEOTIDE SEQUENCE; PEDIGREE; PRESCHOOL CHILD; URINE;

ADULT; AQUAPORIN 2; CASE-CONTROL STUDIES; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FAMILY; FEMALE; HUMANS; HYPONATREMIA; INAPPROPRIATE ADH SYNDROME; INFANT; MALE; PEDIGREE; RECEPTORS, VASOPRESSIN; VASOPRESSINS;

EID: 77956589362     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2009-2524     Document Type: Article

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