Autosomal recessive polycystic kidney disease in adulthood

Nephrology Dialysis Transplantation

Volumn 16, Issue 8, 2001, Pages 1648-1652

  Fonck, Catherine ^a,b   Chauveau, Dominique ^a   Gagnadoux, Marie France ^a   Pirson, Yves ^b   Grünfeld, Jean Pierre ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

^b CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

Author keywords

Adulthood; Autosomal recessive polycystic kidney disease; Congenital hepatic fibrosis; Portal hypertension; Renal failure

Indexed keywords

CREATININE;

ADULT; ADULTHOOD; ARTICLE; BILE DUCT CARCINOMA; CHILD; CHOLANGITIS; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; CREATININE CLEARANCE; DIAGNOSTIC IMAGING; DIALYSIS; DISEASE COURSE; DISEASE SEVERITY; ENDOSCOPY; ESOPHAGUS HEMORRHAGE; EVALUATION; FEMALE; FOLLOW UP; HUMAN; HYPERTENSION; INFANCY; INFANT; KIDNEY COLLECTING TUBULE; KIDNEY CYST; KIDNEY FAILURE; KIDNEY FUNCTION; KIDNEY POLYCYSTIC DISEASE; KIDNEY TRANSPLANTATION; LIVER DISEASE; LIVER FIBROSIS; LIVER FUNCTION TEST; MALE; MORTALITY; NEWBORN; PORTAL HYPERTENSION; PORTOSYSTEMIC ANASTOMOSIS; PRIORITY JOURNAL; PROBABILITY; RECESSIVE INHERITANCE; RECURRENT DISEASE; STOMACH HEMORRHAGE; SURVIVAL; ULTRASOUND;

EID: 0034865003     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/16.8.1648     Document Type: Article

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