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Course and treatment of autosomal dominant polycystic kidney disease
Diagnosis of and screening for autosomal dominant polycystic kidney disease
Extrarenal manifestations of autosomal dominant polycystic kidney disease
Genetics of autosomal dominant polycystic kidney disease and mechanisms of cyst growth
Hypertension in autosomal dominant polycystic kidney disease
Prenatal sonographic diagnosis of cystic renal disease
Renal manifestations of autosomal dominant polycystic kidney disease
Screening for intracranial aneurysm
Urinary tract infection in autosomal dominant polycystic kidney disease
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Metabolic/Endocrine: Decreased glucose tolerance (see PRECAUTIONS ), increased serum levels of low-density lipoproteins and decreased levels of high-density lipoproteins (see PRECAUTIONS , Laboratory Tests ), increased creatine and creatinine excretion, increased serum levels of creatinine phosphokinase (CPK). Reversible changes in liver function tests also occur, including increased Bromsulphalein (BSP) retention and increases in serum bilirubin , glutamic-oxaloacetic transaminase ( SGOT ), and alkaline phosphatase .