Bartter syndrome prenatal diagnosis based on amniotic fluid biochemical analysis

Pediatric Research

Volumn 67, Issue 3, 2010, Pages 300-303

  Garnier, Arnaud ^a   Dreux, Sophie ^b   Vargas Poussou, Rosa ^c,d   Oury, Jean François ^b   Benachi, Alexandra ^d,e   Deschênes, Georges ^a   Muller, Françoise ^b,f  

^a Nephrologie Pediatrique   (France)

^b HÔPITAL ROBERT DEBRÉ   (France)

^c HÔPITAL EUROPÉEN GEORGES POMPIDOU   (France)

^d UNIVERSITÉ PARIS DESCARTES   (France)

^e HÔPITAL NECKER ENFANTS MALADES   (France)

^f University of Paris Ile de France Ouest   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA FETOPROTEIN; ELECTROLYTE; PROTEIN;

AMNION FLUID ANALYSIS; ARTICLE; BARTTER SYNDROME; CLINICAL ARTICLE; CONTROLLED STUDY; ELECTROLYTE BLOOD LEVEL; FEMALE; GESTATIONAL AGE; HUMAN; HYDRAMNIOS; INFANT; MALE; PREDICTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; RETROSPECTIVE STUDY;

ALPHA-FETOPROTEINS; AMNIOTIC FLUID; BARTTER SYNDROME; BIOLOGICAL MARKERS; CASE-CONTROL STUDIES; EARLY DIAGNOSIS; ELECTROLYTES; FEMALE; FETAL PROTEINS; GENETIC PREDISPOSITION TO DISEASE; GESTATIONAL AGE; HUMANS; MALE; PREDICTIVE VALUE OF TESTS; PREGNANCY; PRENATAL DIAGNOSIS; RETROSPECTIVE STUDIES; SENSITIVITY AND SPECIFICITY;

EID: 76749107013     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1203/PDR.0b013e3181ca038d     Document Type: Article

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