Results 131 to 140 of about 17,457 (176)

Caroli disease associated with autosomal recessive polycystic kidney disease: CT imaging features of a case report. [PDF]

Radiol Case Rep
Aien MT, Osmani H, Haqyar MI.
europepmc   +1 more source

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

Pathophysiological significance of cholesterol in ciliopathies. [PDF]

Fujita Med J
Itabashi T, Morita T, Hirosawa M, Kobayashi D, Hasan A, Kimura S, Itoh H, Miyamoto T.   +7 more
europepmc   +1 more source

CART for ascites accumulation and dialysis difficulty after hepatic cyst fenestration and bilateral nephrectomy in ADPKD: a case report. [PDF]

CEN Case Rep
Sawada S, Sugahara S, Sumii A, Sakae T, Yamada A, Imamura-Uehara Y, Ishimoto N, Kuwagata S, Yamahara K, Yasuda-Yamahara M, Tanaka-Sasaki Y, Chin-Kanasaki M, Kume S.   +12 more
europepmc   +1 more source

Tolvaptan for Autosomal Dominant Polycystic Kidney Disease: Real-World Insights from a Propensity Score Weighted Retrospective Cohort Study.

Am J Nephrol
Marshall WR, Chinnadurai R, Rengarajan S, De Bhailís Á, Gorton J, Kalra PA, Wood G.   +6 more
europepmc   +1 more source

Long-Term Tolvaptan Administration in Chinese Patients with Autosomal Dominant Polycystic Kidney Disease: A Retrospective Study in Real Clinical Practice.

Kidney Blood Press Res
Li M, Sun M, Cui S, Liu X, Guo M, Xiao Y, Huang Y, Zhou S, Wang H, Chen X, Li Q.   +10 more
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

2025 KDIGO Executive Summary: Diagnosis and Management of Pediatric Autosomal Dominant Polycystic Kidney Disease.

Kidney Blood Press Res
Subhash S, Safadi A, Bajpai R, Raina R.
europepmc   +1 more source

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Autosomal Dominant Polycystic Kidney Disease

Primary Care: Clinics in Office Practice, 2020
Autosomal 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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Pregnancy in Autosomal Dominant Polycystic Kidney Disease

Advances in Kidney Disease and Health, 2023
Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disorder occurring in approximately 1:1000 individuals. ADPKD is characterized by gradual cyst expansion and kidney enlargement and is a slowly progressive disorder where patients typically initiate renal replacement therapy in the sixth decade of life.
Mina, Al Sayyab, Arlene, Chapman
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