Results 231 to 240 of about 53,957 (281)

A Review of the Management of Nephrolithiasis in Autosomal Dominant Polycystic Kidney Disease. [PDF]

Cureus
Raveendran R, Murali V, Fernando H.
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Trajectories of Kidney Function in Autosomal Dominant Polycystic Kidney Disease Patients Treated with Tolvaptan. [PDF]

Medicina (Kaunas)
Jankowska Z, Niemczyk M.
europepmc   +1 more source

GLIS3, a novel regulator of eicosanoid gene expression and metabolism in normal kidney and polycystic kidney disease. [PDF]

Biochem Pharmacol
Srivastava C, Kang HS, Edin ML, Mukherjee T, Lih FB, Grimm SA, Collier JB, Zeldin DC, Jetten AM.   +8 more
europepmc   +1 more source

Congenital Hepatic Fibrosis and/or Autosomal Recessive Polycystic Kidney Disease: A Single-center Experience. [PDF]

Pediatr Gastroenterol Hepatol Nutr
Altay D, Yel S, Dursun İ, Arslan D.
europepmc   +1 more source

Canadian Society of Nephrology Commentary on the 2025 Kidney Disease Improving Global Outcomes Clinical Practice Guidelines for Autosomal Dominant Polycystic Kidney Disease. [PDF]

Can J Kidney Health Dis
Lanktree MB, Ashawasega N, Bevilacqua M, Bichet DG, Bollée G, Brown PA, Girard L, Goodyer P, Hingwala J, Lemaire M, McFarlane P, Moist L, Pei Y, Proulx N, Schott C, Soroka S, Vlasschaert C, Watkins N, Alam A.   +18 more
europepmc   +1 more source

Retroperitoneoscopic Nephrectomy at the Time of Kidney Transplantation for Autosomal Dominant Polycystic Kidney Disease: Safety, Efficacy, Feasibility, and Cosmetic Outcomes. [PDF]

Transplant Direct
Ohyama T, Nishida S, Minamisono K, Nakao T, Iwami D.   +4 more
europepmc   +1 more source

Pentosidine and Bone Properties in Autosomal Dominant Polycystic Kidney Disease. [PDF]

J Clin Med
Jankowska M, Qureshi AR, Haarhaus M, Magnusson P, Dębska-Ślizień A, Barany P, Heimburger O, Stenvinkel P, Lindholm B.   +8 more
europepmc   +1 more source

Machine Learning Prediction of Progression to Dialysis in Patients With Polycystic Kidney Disease: Population-Based Retrospective Cohort Study. [PDF]

JMIR Med Inform
Chang CH, Chen M, Tsai MH, Huang YC, Liou HH, Shia BC, Liang C, Fang YW.   +7 more
europepmc   +1 more source

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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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