KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease.

doi:10.1111/nep.12658

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Article

KHA-CARI guideline recommendations for the diagnosis and management of autosomal dominant polycystic kidney disease.

Nephrology (Carlton, Vic.) - 1 Aug 2016

Rangan Gopala K, Alexander Stephen I, Campbell Katrina L, Dexter Mark Aj, Lee Vincent W, Lopez-Vargas Pamela, Mai Jun, Mallett Andrew, Patel Chirag, Patel Manish, Tchan Michel C, Tong Allison, Tunnicliffe David J, Vladica Philip, Savige Judy

Abstract excerpt

No abstract is available from the source.

Topics

Adolescent
Adult
Algorithms
Combined Modality Therapy
Critical Pathways
Diagnostic Imaging
Genetic Counseling
Genetic Markers
Genetic Predisposition to Disease
Genetic Testing
Humans
Middle Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Mutation

Nephrology

Phenotype

Polycystic Kidney, Autosomal Dominant

Predictive Value of Tests

TRPP Cation Channels

Source

Open in PubMed

Identifiers

PMID: 26511892
DOI: 10.1111/nep.12658

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