Autosomal-dominant polycystic kidney disease in infancy and childhood: Progression and outcome

Kidney International

Volumn 68, Issue 5, 2005, Pages 2218-2224

  Shamshirsaz, Abdollah ^b   Bekheirnia, Reza M ^b   Kamgar, Mohammad ^b   Johnson, Ann M ^b   McFann, K ^b   Cadnapaphornchai, Melissa ^b   Haghighi, N N ^b   Schrier, Robert W ^a  

^a UNIVERSITY OF COLORADO   (United States)

^b NONE

Author keywords

ADPKD; Childhood; Disease progression

Indexed keywords

ADOLESCENT; AUTOSOMAL DOMINANT DISORDER; CHILD; CHILDHOOD DISEASE; CONFERENCE PAPER; CONTROLLED STUDY; CYST; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE PREDISPOSITION; FEMALE; FOLLOW UP; HEMATURIA; HUMAN; HYPERTENSION; INFANT; INFANT DISEASE; KIDNEY FAILURE; KIDNEY FUNCTION; KIDNEY MASS; KIDNEY POLYCYSTIC DISEASE; MAJOR CLINICAL STUDY; MALE; OUTCOME ASSESSMENT; PRIORITY JOURNAL; PROGNOSIS; PROTEINURIA; SYMPTOM;

ADOLESCENT; AGE OF ONSET; CHILD; CHILD, PRESCHOOL; DISEASE PROGRESSION; FEMALE; FOLLOW-UP STUDIES; HEMATURIA; HUMANS; HYPERTENSION, RENAL; INFANT; KIDNEY FAILURE, CHRONIC; MALE; MASS SCREENING; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; PROTEINURIA; URINE;

EID: 30944440481     PISSN: 00852538     EISSN: 15231755     Source Type: Journal    
DOI: 10.1111/j.1523-1755.2005.00678.x     Document Type: Conference Paper

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