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Ureteric stents has been widely used in kidney transplantation practice to decrease major urologic complications. However ureteral stenting is associated with some specific complications in patients with kidney transplan...

Medullary sponge kidney (MSK) is known as a congenital disesase with dilatation of collecting tubules. MSK is usually asymptomatic but various clinical manifestations may occur including nephrocalcinosis, renal tubular a...

Primary hyperoxaluria is a rarely encountered disease characterised by recurrent urolithiasis, nephrocalcinosis, and oxalate deposition in almost all tissues, generally inherited in autosomal recessive fashion and the im...

OBJECTIVE: Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common hereditary kidney disease. We presented the ADPKD patients who were not undergoing replacement therapy. MATERIAL and METHODS: Accordin...

OBJECTIVE: To report a series of children with duplicated collecting system (DCS) and associated problems. MATERIAL and METHODS: The data of patients with DCS between 1996 and 2011 was reviewed retrospectively. RESUL...

A periodic metagate is designed on top of a boron nitride-graphene heterostructure to modulate the local carrier density distribution on the monolayer graphene. This causes the bandgaps of graphene surface plasmon polari...

Acute renal failure (ARF) is a clinical situation that renal functions deteriorate suddenly within hours to days. Postrenal causes are responsible for a small part of ARF. In this article, we presented a case gone to lef...

A 16 year old boy with end stage renal disease secondary to bilateral urolithiasis underwent bilateral nephrectomy because of recurrent urinary tract infections.Histopathologic examination of the renal tissue was compati...

Type 1 glycogen storage disease is caused by glucose-6-phosphatase deficiency and nephrolithiasis is the most common renal complication. Although urate stones are the most common stone type, metabolic alterations favorin...