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Cardiovascular Autonomic Control in Normotensive Patients with Autosomal Dominant Polycystic Kidney Disease. [PDF]
Rocha DR +6 more
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Cardiac complications in autosomal dominant polycystic kidney disease: links to genotype and CKD severity. [PDF]
Condello G +9 more
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In-depth 3D exploration of autosomal dominant polycystic kidney disease through light sheet fluorescence microscopy. [PDF]
Delgado-Rodriguez P +10 more
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Minocycline infusion sclerotherapy for infected hepatic cysts in a patient with autosomal dominant polycystic kidney disease: a case report and literature review. [PDF]
Inamura Y +4 more
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Autosomal Dominant Polycystic Kidney Disease
New England Journal of Medicine, 1990Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disease occurring in 1 in 200 to 1 in 1,000 individuals. ADPKD is characterized by cystic lesions in the kidneys and often by structural abnormalities in the gastrointestinal tract and cardiovascular system.
P. Gabow
semanticscholar +5 more sources
Autosomal dominant polycystic kidney disease
The Lancet, 2007Autosomal 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 modifier genes.
Vicente E, Torres +2 more
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Autosomal dominant polycystic kidney disease.
American family physician, 2014Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited cause of kidney disease. Enlarging cysts within the kidneys are the clinical hallmark of the disease. Renal manifestations include varying degrees of kidney injury, urinary tract infections, kidney stones, and hematuria.
Ajay, Srivastava, Neel, Patel
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[Autosomal-dominant polycystic kidney disease].
Deutsche medizinische Wochenschrift (1946), 1992G, Fick, M, Weber
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