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New options in the treatment of autosomal dominant polycystic kidney disease.

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dc.contributor.authorKazancioglu, RÜMEYZA
dc.contributor.authorGURSU, MELTEM
dc.contributor.institutionauthorKAZANCIOĞLU, RÜMEYZA
dc.contributor.institutionauthorGÜRSU, MELTEM
dc.date.accessioned2019-10-05T15:34:16Z
dc.date.available2019-10-05T15:34:16Z
dc.date.issued2015-05-01
dc.description.abstractAutosomal dominant polycystic disease (ADPKD) is one of the most common monogenic disorders, and globally is among the most common hereditary causes of end stage kidney disease. Until recently, the causes of this disease remained obscure. However, in the past decade there have been enormous advances in the understanding of the pathophysiology and genetics of this condition, and recent studies have suggested the possibility of specific treatment for slowing cyst growth. This review will focus on the new options for the control of ADPKD.
dc.identifier
dc.identifier.citationKazancioglu R., GURSU M., -New options in the treatment of autosomal dominant polycystic kidney disease.-, Renal failure, cilt.37, ss.535-41, 2015
dc.identifier.pubmed25682970
dc.identifier.trdizintrdizin
dc.identifier.urihttps://hdl.handle.net/20.500.12645/6351
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.3109/0886022X.2015.1013404
dc.language.isoen
dc.subjectkidney disease
dc.titleNew options in the treatment of autosomal dominant polycystic kidney disease.
dc.typeArticle
dspace.entity.typePublication
local.article.journalnameSpor Hekimliği Dergisi
local.avesis.id9e3887cf-116e-4b90-a76c-a650580422a8
local.avesis.response6223
relation.isAuthorOfPublicationeca7bd30-6b6e-444d-96ae-2961c39f2107
relation.isAuthorOfPublicationa6446eac-0ccd-4457-9227-3fc72dec68d1
relation.isAuthorOfPublication.latestForDiscoverya6446eac-0ccd-4457-9227-3fc72dec68d1
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