Results 221 to 230 of about 37,931 (246)

Case Report: A potentially pathogenic new variant of the REN gene found in a family experiencing autosomal dominant tubulointerstitial kidney disease. [PDF]

Front Pediatr
Ma J, Hu Z, Liu Q, Li J, Li J.
europepmc   +1 more source

Renoprotective effects of combination therapy with tolvaptan and dapagliflozin in autosomal dominant polycystic kidney disease: a four-case series. [PDF]

CEN Case Rep
Nishida J, Yamakawa M, Miura S, Yasutomi M.   +3 more
europepmc   +1 more source

GLPG2737, a CFTR Inhibitor, Prevents Cyst Growth in Preclinical Models of Autosomal Dominant Polycystic Kidney Disease.

Am J Nephrol
Dumont V, Meurisse S, Verdonck K, Salgues V, Robert T, Anquetil F, Delachaume C, Blanqué R, Liekens D, Huang Y, Hu J, Harris PC, Nakhlé J, Conrath K, Vandeghinste N, Christophe T, Comas D.   +16 more
europepmc   +1 more source

Autosomal dominant polycystic kidney disease [PDF]

Disease-a-Month, 2015
Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disease of the kidneys that can cause an irreversible decline in kidney function leading to end-stage renal disease. It is one of the most common hereditary disorders. It is 10 times more common than sickle cell disease and 20 times more common than Huntington's disease.
Edgar V. Lerma, Jonathan Silverman, Chaitanya Desai   +2 more
openaire   +5 more sources

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Assessing Risk of Rapid Progression in Autosomal Dominant Polycystic Kidney Disease and Special Considerations for Disease-Modifying Therapy.

American Journal of Kidney Diseases, 2021
Autosomal Dominant Polycystic Kidney Disease is the most common inherited cause of kidney failure accounting for 5-10% of cases. Predicting which patient would progress rapidly to kidney failure is critical to assess the risk-benefit ratio of any ...
F. Chebib, V. Torres
semanticscholar   +1 more source

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
openaire   +4 more sources

Prescribed Water Intake in Autosomal Dominant Polycystic Kidney Disease

NEJM Evidence, 2021
Prescribed Water Intake in Autosomal Dominant Polycystic Kidney Disease The effect of increased water intake on kidney cyst growth in patients with polycystic kidney disease was compared for two groups randomly assigned to either prescribed or ad libitum
Gopi Rangan, Annette Wong, A. Munt, Jennifer Zhang, S. Saravanabavan, Margaret Allman-Farinelli, Sunil V. Badve, Neil Boudville, Bradley J. Erickson, Mangalee R. Fernando, Sheryl L. Foster, Adriana Gregory, I. Haloob, Carmel M. Hawley, David W. Johnson, Timothy L. Kline, Vincent W. Lee, Maureen A. Lonergan, Elaine Pascoe, A. Rangan, Simon D Roger, Kamal Sud, Vicente E. Torres, Sundareswari V. Adinarayanan, D. Harris   +24 more
semanticscholar   +1 more source