Disease | autosomal dominant polycystic kidney disease |
Symptom | C0022679|renal cyst |
Sentences | 10 |
PubMedID- 23304619 | Some experimental studies have suggested a beneficial effect of the mammalian target of rapamycin (mtor) inhibitor use on hepatic and renal cyst growth in patients with autosomal dominant polycystic kidney disease (adpkd). |
PubMedID- 22127398 | A potential salvage therapy for refractory renal cyst infection in patients with autosomal dominant polycystic kidney disease. |
PubMedID- 25634914 | A management algorithm for large renal cyst in autosomal dominant polycystic kidney disease (adpkd) is lacking despite the potential to cause widespread medical and surgical complications. |
PubMedID- 21206992 | It has been suggested that more than 70% of the renal cysts in patients with autosomal dominant polycystic kidney disease (adpkd) arise from the collecting duct and that within this segment cysts originate almost exclusively from principal rather than intercalated cells. |
PubMedID- 21697238 | We previously showed that ouabain induces proliferation of epithelial cells derived from renal cysts of patients with autosomal dominant polycystic kidney disease (adpkd cells). |
PubMedID- 25931844 | Acute abdomen and hemorrhagic shock caused by spontaneous rupture of renal cyst in autosomal dominant polycystic kidney disease. |
PubMedID- 23784065 | Cells derived from renal cysts of patients with autosomal dominant polycystic kidney disease (adpkd) are abnormally sensitive to ouabain, responding to physiological ouabain concentrations with enhanced proliferation and increased forskolin-induced transepithelial fluid secretion. |
PubMedID- 24674583 | Cd1(pcy/pcy) (pcy) mice have a slowly progressive disease phenotype that resembles human autosomal dominant polycystic kidney disease with renal cyst formation and inflammation. |
PubMedID- 22391500 | Retention of iodinated contrast material within renal cysts in a patient with autosomal dominant polycystic kidney disease. |
PubMedID- 22710499 | Refractory salmonella enterica serotype choleraesuis-related renal cyst infection in a patient with autosomal dominant polycystic kidney disease undergoing hemodialysis treated successfully with intracystic ciprofloxacin infusion. |
Page: 1