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Baseline comorbidity of cardiovascular-kidney-metabolic syndrome increases the risk of adverse clinical outcomes in patients with chronic kidney disease. [PDF]
Front Endocrinol (Lausanne)Meng J, Li W, Fu W, Zhang A.
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Comprehensive Physiology, 2017
ABSTRACTRenal cysts, which arise from renal tubules, can be seen in a variety of hereditary and nonhereditary entities. Common mechanisms associated with renal cyst formation include increased cell proliferation, epithelial fluid secretion, and extracellular matrix remodeling.
Benjamin D. Cowley, Joseph Ghata
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ABSTRACTRenal cysts, which arise from renal tubules, can be seen in a variety of hereditary and nonhereditary entities. Common mechanisms associated with renal cyst formation include increased cell proliferation, epithelial fluid secretion, and extracellular matrix remodeling.
Benjamin D. Cowley, Joseph Ghata
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New England Journal of Medicine, 2004
Polycystic kidney diseases are inherited renal disorders due mainly to mutations in genes that regulate the development and function of cells that line renal tubules. This review outlines the clinical importance of polycystic kidney diseases and discusses the cell biology and molecular mechanisms that cause the formation of hundreds of cystic lesions ...
Thomas C. Hart, Anthony J. Bleyer
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Polycystic kidney diseases are inherited renal disorders due mainly to mutations in genes that regulate the development and function of cells that line renal tubules. This review outlines the clinical importance of polycystic kidney diseases and discusses the cell biology and molecular mechanisms that cause the formation of hundreds of cystic lesions ...
Thomas C. Hart, Anthony J. Bleyer
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InnovAiT: Education and inspiration for general practice, 2020
Polycystic kidney disease (PKD) is a monogenic, hereditary disorder of the kidneys that leads to fluid-filled cysts within the renal tubes. It is one of the most common causes of end-stage renal failure. There are two types, the more common autosomal dominant (ADPKD) and the rarer autosomal recessive (ARPKD).
Soo Oh, Rabeet Khan, Ahmed Ziada
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Polycystic kidney disease (PKD) is a monogenic, hereditary disorder of the kidneys that leads to fluid-filled cysts within the renal tubes. It is one of the most common causes of end-stage renal failure. There are two types, the more common autosomal dominant (ADPKD) and the rarer autosomal recessive (ARPKD).
Soo Oh, Rabeet Khan, Ahmed Ziada
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Polycystic Disease of the Kidneys
Annals of Internal Medicine, 1928Excerpt Although polycystic degeneration of the kidneys cannot be looked upon a rare disease, it may be regarded as relatively uncommon.
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2014
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited renal disorder and monogenic cause of hypertension. ADPKD should be considered in any patient presenting with bilateral renal cysts particularly if there is associated hypertension.
Lewis, Gareth, Maxwell, Alexander P.
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Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited renal disorder and monogenic cause of hypertension. ADPKD should be considered in any patient presenting with bilateral renal cysts particularly if there is associated hypertension.
Lewis, Gareth, Maxwell, Alexander P.
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2011
A 42-year-old woman presented for additional evaluation of autosomal dominant polycystic kidney disease (ADPKD). She was initially diagnosed with ADPKD at age 36 after developing fever and flank pain. At that time, ultrasonography showed bilateral renal cysts, and liver and ovarian cysts. The serum creatinine level was normal.
Ying-Cai Tan +3 more
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A 42-year-old woman presented for additional evaluation of autosomal dominant polycystic kidney disease (ADPKD). She was initially diagnosed with ADPKD at age 36 after developing fever and flank pain. At that time, ultrasonography showed bilateral renal cysts, and liver and ovarian cysts. The serum creatinine level was normal.
Ying-Cai Tan +3 more
openaire +2 more sources