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Genetic testing in autosomal dominant polycystic kidney disease: why it matters in 2025. [PDF]
Cornec-Le Gall E, Ong ACM.
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Clinical Factors Associated With Intracranial Aneurysms in Patients With Autosomal Dominant Polycystic Kidney Disease. [PDF]
Fuchinoue Y +7 more
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Unravelling sex-specific differences in autosomal dominant polycystic kidney disease: a multiorgan perspective. [PDF]
Furlano M +9 more
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Quantitative dynamic contrast-enhanced magnetic resonance imaging for renal perfusion measurement in autosomal dominant polycystic kidney disease. [PDF]
Onuoha EE +4 more
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Angiotensin Blockade Beyond Hypertension in Autosomal Dominant Polycystic Kidney Disease
Jing Xu +6 more
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Autosomal Dominant Polycystic Kidney Disease
Primary Care: Clinics in Office Practice, 2020Autosomal 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
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Autosomal dominant polycystic kidney disease
Disease-a-Month, 2015Autosomal 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
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Autosomal dominant polycystic kidney disease
The Lancet, 2019Autosomal 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
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