Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Manish Kumar Agarwal"'
Publikováno v:
African Journal of Urology, Vol 28, Iss 1, Pp 1-5 (2022)
Abstract Background Synovial sarcoma is a rare type of sarcoma with a predilection for extremities in young adults. Very rarely this tumor can originate from kidney. Case presentation A 22-year-old female presented to us with complaints of right flan
Externí odkaz:
https://doaj.org/article/86fd63d3c1574c5990e002ce5b378fab
Publikováno v:
Urology Annals, Vol 12, Iss 1, Pp 54-56 (2020)
Introduction: In the present era, percutaneous nephrolithotomy (PCNL) is the standard treatment for large (>2 cm) renal or staghorn renal stones. Both air and iodinated contrast has been used to opacify the pelvicalyceal system (PCS) before the dilat
Externí odkaz:
https://doaj.org/article/26aca5b481504745aac609231ef07e26
Publikováno v:
Urology Annals, Vol 8, Iss 3, Pp 384-386 (2016)
Pheochromocytoma is a catecholamine secreting tumor that originate from chromaffin cells. Usually, it is solid neoplasm of the adrenal medulla, however cystic pheochromocytoma is a rare neuro-endocrine tumour that is frequently asymptomatic and often
Externí odkaz:
https://doaj.org/article/b4580d0275c84e7da8a02e4776dfedcf
Publikováno v:
Urology Annals
Urology Annals, Vol 12, Iss 1, Pp 54-56 (2020)
Urology Annals, Vol 12, Iss 1, Pp 54-56 (2020)
Introduction: In the present era, percutaneous nephrolithotomy (PCNL) is the standard treatment for large (>2 cm) renal or staghorn renal stones. Both air and iodinated contrast has been used to opacify the pelvicalyceal system (PCS) before the dilat
Publikováno v:
MTV
In todays advanced System on Chip (SoCs), system interconnects and memories are the most common shared resources on which System and Intellectual Property (IP) performance depends heavily. In real applications, when these shared resources are used by
Publikováno v:
Urology Annals
Urology Annals, Vol 8, Iss 3, Pp 384-386 (2016)
Urology Annals, Vol 8, Iss 3, Pp 384-386 (2016)
Pheochromocytoma is a catecholamine secreting tumor that originate from chromaffin cells. Usually, it is solid neoplasm of the adrenal medulla, however cystic pheochromocytoma is a rare neuro-endocrine tumour that is frequently asymptomatic and often