Renal tubular dysgenesis, a not uncommon autosomal recessive disorder leading to oligohydramnios: Role of the renin-angiotensin system

Journal of the American Society of Nephrology

Volumn 17, Issue 8, 2006, Pages 2253-2263

  Lacoste, Mireille ^a   Cai, Yi ^a   Guicharnaud, Liliane ^a   Mounier, Françoise ^a   Dumez, Yves ^b   Bouvier, Raymonde ^f   Dijoud, Frédérique ^g   Gonzales, Marie ^c   Chatten, Jane ^h   Delezoide, Anne Lise ^d   Daniel, Laurent ⁱ   Joubert, Madeleine ^j   Laurent, Nicole ^k   Aziza, Jacqueline ^l   Sellami, Tahya ^m   Ben Amar, Hatem ⁿ   Jarnet, Catherine ^o   Frances, Anne Marie ^p   Daïkha Dahmane, Farida ^q   Coulomb, Aurore ^r   Neuhaus, Thomas J ^s   Foliguet, Bernard ^t   Chenal, Pierre ^u   Marcorelles, Pascale ^v   Gasc, Jean Marie ^e   Corvol, Pierre ^e   Gubler, Marie Claire ^a,b   more..

^a INSERM   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c HÔPITAL SAINT ANTOINE   (France)

^d HÔPITAL ROBERT DEBRÉ   (France)

^e l'alimentation et l'Environnement   (France)

^f EDOUARD HERRIOT HOSPITAL   (France)

^g HÔPITAL DEBROUSSE   (France)

^h CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

ⁱ TIMONE HOSPITAL   (France)

^j HÔTEL DIEU   (France)

^k DIJON UNIVERSITY HOSPITAL   (France)

^l CHU PURPAN   (France)

^m HABIB BOURGUIBA HOSPITAL   (Tunisia)

ⁿ HEDI CHAKER HOSPITAL   (Tunisia)

^o Centre Hospitalier Intercommunal   (France)

^p Hôpital Font Pré   (France)

^q CENTRE HOSPITALIER INTERCOMMUNAL   (France)

^r HÔPITAL ANTOINE BÉCLÈRE   (France)

^s UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

^t Secteur de Foetopathologie   (France)

^u Maternite Regionale Universitaire   (France)

^v BREST UNIVERSITY HOSPITAL   (France)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOTENSIN 2 RECEPTOR; ANGIOTENSINOGEN; DIPEPTIDYL CARBOXYPEPTIDASE; RENIN;

ANURIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; AUTOSOMAL RECESSIVE INHERITANCE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE SEVERITY; EARLY DIAGNOSIS; FAMILIAL DISEASE; FEMALE; FETUS; FETUS DEVELOPMENT; GENE MUTATION; GENETIC COUNSELING; GENETIC HETEROGENEITY; GENETIC LINKAGE; GESTATION PERIOD; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; HYPOXIA; KIDNEY DEVELOPMENT; KIDNEY FUNCTION; KIDNEY MALFORMATION; LUNG HYPOPLASIA; MALE; NEWBORN; OLIGOHYDRAMNIOS; PERINATAL DEATH; POTTER SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; RENAL ARTERY; RENAL TUBULAR DYSGENESIS; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; SKULL MALFORMATION;

EID: 33746533123     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: 10.1681/ASN.2005121303     Document Type: Article

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