Results 121 to 130 of about 1,110,820 (300)

THE AFTER-HISTORY OF A CASE OF NEPHRECTOMY FOR POLYCYSTIC KIDNEY [PDF]

, 1929
H. Temple Mursell
openalex   +1 more source

Targeting the vasopressin type-2 receptor for renal cell carcinoma therapy. [PDF]

, 2020
Arginine vasopressin (AVP) and its type-2 receptor (V2R) play an essential role in the regulation of salt and water homeostasis by the kidneys. V2R activation also stimulates proliferation of renal cell carcinoma (RCC) cell lines in vitro.
Calvet, James P, Dwivedi, Nidhi, Enders, Jonathan, Jamadar, Abeda, Kakade, Vijayakumar R, Neil, Maura O', Rao, Reena, Sinha, Sonali, Tao, Shixin, Thomas, Sufi M, Weiss, Robert H   +10 more
core  

Hypernephroma in a Polycystic Kidney: Case Report [PDF]

, 1945
William Baurys
openalex   +1 more source

Prevalence of autosomal dominant polycystic kidney disease in the European Union

Nephrology, Dialysis and Transplantation, 2016
Background Autosomal dominant polycystic kidney disease (ADPKD) is a leading cause of end-stage renal disease, but estimates of its prevalence vary by >10-fold.
C. Willey, J. Blais, A. Hall, H. Krasa, A. J. Makin, F. Czerwiec   +5 more
semanticscholar   +1 more source

Case Report: Autosomal dominant polycystic kidney disease and Wilms’ tumor in infancy and childhood

Frontiers in Pediatrics
BackgroundAutosomal dominant polycystic kidney disease (ADPKD) is rare but one of the most common inherited kidney diseases. Normal kidney function is maintained until adulthood in most patients.
Doviltyte Zina, Doviltyte Zina, Kiudeliene Rosita, Kiudeliene Rosita, Zviniene Kristina, Zviniene Kristina, Rutkauskiene Giedre, Rutkauskiene Giedre, Masalskiene Jurate, Masalskiene Jurate   +9 more
doaj   +1 more source

Rationale and design of the RESOLVE trial: lanreotide as a volume reducing treatment for polycystic livers in patients with autosomal dominant polycystic kidney disease

BMC Nephrology, 2012
Background A large proportion of patients with autosomal dominant polycystic kidney disease (ADPKD) suffers from polycystic liver disease. Symptoms arise when liver volume increases.
Gevers Tom JG, Chrispijn Melissa, Wetzels Jack FM, Drenth Joost PH   +3 more
doaj   +1 more source

Discussion on Polycystic Disease of the Kidneys [PDF]

, 1924
Graham J. Forbes
openalex   +1 more source

Caroli′s syndrome in a post renal transplant patient: Case report and review of the literature

The Saudi Journal of Gastroenterology, 2012
Caroli′s syndrome is characterized by bile duct ectasia in association with hepatic fibrosis. It is usually transmitted in an autosomal recessive fashion and has been well documented to be associated with autosomal recessive polycystic kidney disease and
Muhammad Z Bawany, Osama Alaradi, Ali Nawras   +2 more
doaj   +1 more source

Polycystic Disease of the Liver, Pancreas and Kidneys [PDF]

, 1939
Manville W. Norton
openalex   +1 more source

Polycystic Kidney Disease without an Apparent Family History.

Journal of the American Society of Nephrology, 2017
The absence of a positive family history (PFH) in 10%-25% of patients poses a diagnostic challenge for autosomal dominant polycystic kidney disease (ADPKD).
Ioan-Andrei Iliuta, Vinusha Kalatharan, Kairong Wang, E. Cornec-Le Gall, J. Conklin, M. Pourafkari, Ryan R. Ting, Chen Chen, A. Borgo, N. He, Xuewen Song, C. M. Heyer, Sarah R. Senum, Y. Hwang, A. Paterson, P. Harris, K. Khalili, Y. Pei   +17 more
semanticscholar   +1 more source