Genotype-phenotype correlation in children with autosomal dominant polycystic kidney disease

Pediatric Nephrology

Volumn 24, Issue 5, 2009, Pages 983-989

  Fencl, Filip ^a   Janda, Jan ^a   Bláhová, Květa ^a   Hříbal, Zdeněk ^a   Štekrová, Jitka ^a   Puchmajerová, Alena ^a   Seeman, Tomáá ^a  

^a CHARLES UNIVERSITY   (Czech Republic)

Author keywords

Autosomal dominant polycystic kidney disease; Blood pressure; Children; Hypertension; PKD1 gene; PKD2 gene; Renal function; Ultrasound

Indexed keywords

CREATININE; POLYCYSTIN 1; POLYCYSTIN 2;

ARTICLE; BLOOD PRESSURE MONITORING; CHILD; CLINICAL ARTICLE; CLINICAL ASSESSMENT; CONTROLLED STUDY; CREATININE CLEARANCE; FEMALE; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HYPERTENSION; INTERMETHOD COMPARISON; KIDNEY CYST; KIDNEY HYPERTROPHY; KIDNEY POLYCYSTIC DISEASE; MALE; PRENATAL PERIOD; PRIORITY JOURNAL; PROTEINURIA; RENOGRAPHY; SCHOOL CHILD; SCORING SYSTEM;

BLOOD PRESSURE; BLOOD PRESSURE MONITORING, AMBULATORY; CHILD; FEMALE; GENOTYPE; HUMANS; HYPERTENSION; KIDNEY; MALE; PHENOTYPE; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; RETROSPECTIVE STUDIES; TRPP CATION CHANNELS;

EID: 63649088502     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-008-1090-9     Document Type: Article

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