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Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists

Because autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic abnormalities seen in today's medical practice, many internists will likely treat patients affected by this condition. Genetic abnormalities have been increasingly recognized, and the pathophysiology...

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Detalles Bibliográficos
Autor principal: Bennett, William M.
Formato: Texto
Lenguaje:English
Publicado: The Korean Association of Internal Medicine 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732773/
https://www.ncbi.nlm.nih.gov/pubmed/19721850
http://dx.doi.org/10.3904/kjim.2009.24.3.165
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author Bennett, William M.
author_facet Bennett, William M.
author_sort Bennett, William M.
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description Because autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic abnormalities seen in today's medical practice, many internists will likely treat patients affected by this condition. Genetic abnormalities have been increasingly recognized, and the pathophysiology of the disease is beginning to be unraveled. Because of advances in imaging technology, surrogate markers for disease progression have allowed clinical studies of newer therapeutic agents to proceed. In the near future, therapies for this common genetic disease may be available to either prevent or stabilize the disease course for many affected individuals.
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spelling pubmed-27327732009-09-01 Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists Bennett, William M. Korean J Intern Med Review Because autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic abnormalities seen in today's medical practice, many internists will likely treat patients affected by this condition. Genetic abnormalities have been increasingly recognized, and the pathophysiology of the disease is beginning to be unraveled. Because of advances in imaging technology, surrogate markers for disease progression have allowed clinical studies of newer therapeutic agents to proceed. In the near future, therapies for this common genetic disease may be available to either prevent or stabilize the disease course for many affected individuals. The Korean Association of Internal Medicine 2009-09 2009-08-26 /pmc/articles/PMC2732773/ /pubmed/19721850 http://dx.doi.org/10.3904/kjim.2009.24.3.165 Text en Copyright © 2009 The Korean Association of Internal Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Bennett, William M.
Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists
title Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists
title_full Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists
title_fullStr Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists
title_full_unstemmed Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists
title_short Autosomal Dominant Polycystic Kidney Disease: 2009 Update for Internists
title_sort autosomal dominant polycystic kidney disease: 2009 update for internists
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2732773/
https://www.ncbi.nlm.nih.gov/pubmed/19721850
http://dx.doi.org/10.3904/kjim.2009.24.3.165
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