Diagnosis of autosomal-dominant polycystic kidney disease: An integrated approach

Seminars in Nephrology

Volumn 30, Issue 4, 2010, Pages 356-365

  Barua, Moumita ^a   Pei, York ^a  

^a UNIVERSITY OF TORONTO   (Canada)

Author keywords

ADPKD; Diagnosis; Screening

Indexed keywords

POLYCYSTIN 1; POLYCYSTIN 2;

ARTICLE; DIAGNOSTIC IMAGING; DIAGNOSTIC TEST; DIFFERENTIAL DIAGNOSIS; DYSOSTOSIS; ECHOGRAPHY; FAMILY HISTORY; GENE MUTATION; GENETIC ASSOCIATION; GENETIC RISK; HUMAN; KIDNEY CYST; KIDNEY FAILURE; KIDNEY POLYCYSTIC DISEASE; MEDULLARY SPONGE KIDNEY; MOLECULAR GENETICS; PRIORITY JOURNAL; TUBEROUS SCLEROSIS; ULTRASOUND; VON HIPPEL LINDAU DISEASE;

ADOLESCENT; ADULT; AGE FACTORS; ALGORITHMS; GENOTYPE; HUMANS; MIDDLE AGED; PEDIGREE; POLYCYSTIC KIDNEY, AUTOSOMAL DOMINANT; TRPP CATION CHANNELS; YOUNG ADULT;

EID: 77956141367     PISSN: 02709295     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.semnephrol.2010.06.002     Document Type: Article

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