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14  Articles
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Congenital giant megaureter presents as abdominal mass and impose diagnostic difficulties. It can be associated with other upper urinary tract anomalies. A female newborn with antenatal diagnosis of polycystic kidneys was admitted at birth due to lower ab... see more

Prune belly syndrome is a rare congenital disorder defined by a characteristicclinical triad: Abdominal muscle deficiency, severe urinary tract abnormalities,and bilateral cryptorchidism. We describe a preterm neonate of Prune Bellysyndrome who had abdomi... see more

Ameloblastoma is a rare odontogenic neoplasm occurring in the jaw that can be observed as several different histologic and radiographic presentations. Since inadequate treatment is associated with high recurrence rate, accurate diagnosis is critical for p... see more

Cystic partially differentiated nephroblastoma (CPDN) is among the rare kidney tumors of childhood. Here, a case of CPDN in a baby who was operated with the diagnosis of multicystic kidney is reported. Clinical and imaging studies have a limited role in t... see more

Benign multicystic peritoneal mesothelioma (BMPM) is an uncommon lesion. It presents as a lump in abdomen or a finding seen on imaging modalities. Surgery is the primary modality of treatment. However, it has a high recurrence rate; this results in adhesi... see more

Introduction: The WHO classifies ameloblastoma as abenign epithelial odontogenic tumor without odontogenicectomesenchyme with locally invasive behaviorand high recurrence rate. It represents 1% of oral tumors,primarily affecting the posterior mandible. Ge... see more

Clear cell (tubulo) papillary renal cell carcinoma (CCPRCC) is a newly established entity in renal tumor classification. Here we report a case of CCPRCC in a 61 year old male with long history of hypertension, chronic renal failure, and one year history o... see more

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