Results 171 to 180 of about 34,123 (218)

Multicystic Kidney Disease in a Family With Tuberous Sclerosis Complex. [PDF]

Nephrology (Carlton)
Donald JS, Edmonstone C, Chan DL, Chung CWT, Kennedy SE.   +4 more
europepmc   +1 more source

Advances and future perspectives of kidney organoid technology in renal disease research and clinical translation. [PDF]

Front Med (Lausanne)
Zhao Z, Tong K, Deng K, Liu H, Li Y, Wang D.   +5 more
europepmc   +1 more source

Medical Management of Polycystic Liver Disease: A Position Statement From the European Reference Network on Hepatological Diseases. [PDF]

Liver Int
Heinrich S, de Matos AMC, Colmenero J, Elsharkawy AM, Fraňková S, Halbritter J, Mrzljak A, Müller RU, Pereira R, Strnad P, Teemer CAJ, Verbeek J, Wronka KM, Nevens F, Taubert R, Drenth JPH, European Reference Network on Hepatological Liver Diseases (ERN RARE‐LIVER).   +16 more
europepmc   +1 more source

Evolution of Clinical Trial Design in ADPKD. [PDF]

Kidney Int Rep
Roth JR, Dahl NK, Garimella PS.
europepmc   +1 more source

Overweight and Obesity Are Associated with Lower Renal Blood Flow in Autosomal Dominant Polycystic Kidney Disease.

Kidney Blood Press Res
Birznieks CL, Wang W, Steele C, You Z, Gitomer B, Chonchol M, Nowak KL.   +6 more
europepmc   +1 more source

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Kynurenines in polycystic kidney disease

Journal of Nephrology, 2022
Abstract Background Autosomal dominant polycystic kidney disease (ADPKD) is a common hereditary disorder, characterized by kidney cyst formation. A major pathological feature of ADPKD is the development of interstitial inflammation.
Jost, Klawitter, Matthew J, Jackson, Peter H, Smith, Katharina, Hopp, Michel, Chonchol, Berenice Y, Gitomer, Melissa A, Cadnapaphornchai, Uwe, Christians, Jelena, Klawitter   +8 more
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Polycystic Kidney Disease

Comprehensive Physiology, 2017
ABSTRACT Renal 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. Hereditary polycystic kidney disease
Joseph, Ghata, Benjamin D, Cowley
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Cilia and polycystic kidney disease

Seminars in Cell & Developmental Biology, 2021
Polycystic kidney disease (PKD), comprising autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD), is characterized by incessant cyst formation in the kidney and liver. ADPKD and ARPKD represent the leading genetic causes of renal disease in adults and children, respectively.
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Polycystic Kidney/Liver Disease

Clinics in Liver Disease, 2022
Autosomal dominant polycystic kidney disease (ADPKD) is a genetic disorder that leads to chronic kidney disease and end-stage kidney disease (ESKD). Polycystic liver disease (PCLD) is the most common extrarenal manifestation of ADPKD. Though isolated PCLD and PCLD due to ADPKD are genetically distinct, they follow a similar clinical course of ...
Rebecca, Roediger, Douglas, Dieterich, Pramodh, Chanumolu, Priya, Deshpande   +3 more
openaire   +2 more sources