Results 171 to 180 of about 21,454 (214)

Unravelling sex-specific differences in autosomal dominant polycystic kidney disease: a multiorgan perspective. [PDF]

open access: yesClin Kidney J
Furlano M   +9 more
europepmc   +1 more source

Angiotensin Blockade Beyond Hypertension in Autosomal Dominant Polycystic Kidney Disease

open access: yes
Jing Xu   +6 more
core   +1 more source

Autosomal Dominant Polycystic Kidney Disease

Primary Care: Clinics in Office Practice, 2020
Autosomal Dominant Polycystic Kidney Disease is an inherited multisystemic disorder of the renal tubules with subsequent formation of multiple cysts and enlargement of the kidney, affecting various organs. Diagnosis is initially suspected in those with family history and/or individuals who develop hypertension early on (secondary hypertension) or ...
Parvathi, Perumareddi, Darin P, Trelka
openaire   +2 more sources

Autosomal dominant polycystic kidney disease

Disease-a-Month, 2015
Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disease of the kidneys that can cause an irreversible decline in kidney function leading to end-stage renal disease. It is one of the most common hereditary disorders. It is 10 times more common than sickle cell disease and 20 times more common than Huntington's disease.
Jonathan, Silverman   +2 more
openaire   +2 more sources

Autosomal dominant polycystic kidney disease

The Lancet, 2019
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and one of the most common causes of end-stage kidney disease. Multiple clinical manifestations, such as enlarged kidneys filled with growing cysts, hypertension, and multiple extrarenal complications, including liver cysts, intracranial aneurysms, and ...
Emilie, Cornec-Le Gall   +2 more
openaire   +2 more sources

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