Browsing by Subject "Renal failure"
Now showing items 1-4 of 4
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Article
A family with the branchio-oto-renal syndrome: Clinical and genetic correlations
(2002)Background. The branchio-oto-renal (BOR) syndrome is an autosomal dominant disease characterized by hearing loss of early onset, preauricular pits, branchial clefts, and early progressive chronic renal failure in up to 40% ...
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Article
Manual and automated intima-media thickness and diameter measurements of the common carotid artery in patients with renal failure disease
(2014)The objective of this study was to investigate differences in intima-media thickness (IMT) and diameter (D) measurements of the common carotid artery (CCA) in ultrasound imaging in normal subjects and renal failure disease ...
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Article
Mutations of the human polycystic kidney disease 2 (PKD2) gene
(2001)Autosomal dominant polycystic kidney disease (ADPKD) is an inherited nephropathy, usually of late onset (onset between third to seventh decade), primarily characterized by the formation of fluid-filled cysts in the kidneys. ...
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Article
Ultrasound intima-media thickness and diameter measurements of the common carotid artery in patients with renal failure disease
(2013)Although the intima-media thickness (IMT) of the common carotid artery (CCA) is an established indicator of cardiovascular disease (CVD), its relationship with renal failure disease (RFD) is not yet established. In this ...