Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Varsha Chhotusing Pardeshi"'
Publikováno v:
BMC Nephrology, Vol 23, Iss 1, Pp 1-10 (2022)
Abstract Background Congenital anomalies of the kidney and urinary tract (CAKUT) cover a spectrum of structural malformations that result from aberrant morphogenesis of kidney and urinary tract. It is the most prevalent cause of kidney failure in chi
Externí odkaz:
https://doaj.org/article/fb268c6a01974f0ab5e416ed7e3ebcfd
Autor:
Stuti Panigrahi, Varsha Chhotusing Pardeshi, Karthikeyan Chandrasekaran, Karthik Neelakandan, Hari PS, Anil Vasudevan
Publikováno v:
Clinical and Experimental Pediatrics, Vol 64, Iss 7, Pp 355-363 (2021)
Background Nephrotic syndrome (NS) is a common renal disorder in children attributed to podocyte injury. However, children with the same diagnosis have markedly variable treatment responses, clinical courses, and outcomes, suggesting molecular hetero
Externí odkaz:
https://doaj.org/article/0bd277734ae54ce6bc74ba8634d5868f
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-10 (2018)
Abstract Background Steroid resistant nephrotic syndrome (SRNS) is a genetically heterogeneous disease with significant phenotypic variability. More than 53 podocyte-expressed genes are implicated in SRNS which complicates the routine use of genetic
Externí odkaz:
https://doaj.org/article/f446e0df13e84d049bdb85f6a200b19c
Publikováno v:
BMC Nephrology
BMC Nephrology, Vol 23, Iss 1, Pp 1-10 (2022)
BMC Nephrology, Vol 23, Iss 1, Pp 1-10 (2022)
Background Congenital anomalies of the kidney and urinary tract (CAKUT) cover a spectrum of structural malformations that result from aberrant morphogenesis of kidney and urinary tract. It is the most prevalent cause of kidney failure in children. He