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Autosomal dominant polycystic kidney disease [PDF]

open access: yesLancet, The, 2007
Autosomal dominant polycystic kidney disease is the most prevalent, potentially lethal, monogenic disorder. It is associated with large interfamilial and intrafamilial variability, which can be explained to a large extent by its genetic heterogeneity and
Vicente E Torres   +2 more
exaly   +6 more sources

Autosomal Dominant Polycystic Kidney Disease [PDF]

open access: yesAdvances in Chronic Kidney Disease, 2010
A 48-year-old man presented for evaluation of the transplantation of a kidney from a living donor. He had a 14-year history of autosomal dominant polycystic kidney disease with progression to end-stage renal disease that required hemodialysis. Initially,
Burcin Ekser   +3 more
core   +5 more sources

Autosomal dominant polycystic kidney disease [PDF]

open access: yesCanadian Medical Association Journal, 2017
Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic disorder which causes end stage renal disease. In Denmark, estimated 5,000 patients are living with the disease.
Jensen, Anja Møller   +3 more
core   +3 more sources

Hypertension in autosomal dominant polycystic kidney disease

open access: yesKidney International, 1988
Hypertension in autosomal dominant polycystic kidney disease. Autosomal dominant polycystic kidney disease (ADPKD) has been shown to be associated with a greater than 50 percent incidence of hypertension prior to deterioration in renal function as ...
Johnson, Ann M.   +5 more
core   +3 more sources

Autosomal dominant polycystic kidney disease in children

open access: yesSaudi Journal of Kidney Diseases and Transplantation, 2016
Autosomal dominant polycystic kidney disease (ADPKD) presenting in adults is well documented, but the presentation in children is uncommon and is unclear why the disease presents early.
S Ramakrishnan   +2 more
core   +6 more sources

Autosomal dominant polycystic kidney

open access: yesPan African Medical Journal, 2022
Polycystic kidney disease is a hereditary illness that causes cystic growth of the kidneys, resulting in increasing kidney enlargement and renal insufficiency, as well as a variety of extrarenal symptoms. The illness has autosomal dominant and recessive inheritance patterns, characterized by gradual but increasing enlargement of the kidneys, with renal
Rugaved Raghavendra Gudadhe   +1 more
openaire   +3 more sources

Autosomal dominant polycystic kidney disease [PDF]

open access: yesClinical Medicine, 2009
Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disease with a prevalence of 1:400 to 1:1,000 live births.[1][1] It is the most common genetic cause of renal failure, accounting for 10% of patients on dialysis.
Chern Li, Chow, Albert C M, Ong
openaire   +2 more sources

Autosomal dominant polycystic kidney disease in hemodialysis patients in southern Brazil [PDF]

open access: yes, 2014
INTRODUCTION: Autosomal dominant polycystic kidney disease is the most common hereditary renal disease in humans. OBJECTIVE: To examine the prevalence, clinical and laboratory characteristics of patients with polycystic kidneys and relate disease ...
Torres, Paulo Roberto Aranha   +17 more
core   +1 more source

Marfan Syndrome and Autosomal Dominant Polycystic Kidney Disease: A Case of Rare Co-occurrence or Coincidence? [PDF]

open access: yes, 2022
Background: Marfan syndrome (MFS) and autosomal dominant kidney disease (ADPKD) are two separate genetic disorders. The author describes the case of a young male with ADPKD who incidentally had Marfan-like features. A literature review was carried out to
Arjun Sekar
core   +1 more source

Urinary proteomic biomarkers for diagnosis and risk stratification of autosomal dominant polycystic kidney disease: a multicentric study [PDF]

open access: yes, 2013
Treatment options for autosomal dominant polycystic kidney disease (ADPKD) will likely become available in the near future, hence reliable diagnostic and prognostic biomarkers for the disease are strongly needed.
Torres, Vicente E.   +101 more
core   +1 more source

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