Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Remi George Thomas"'
Autor:
Balaraman Velayudham, Remi George Thomas, C Vasudevan, R P Senthilkumar, Thirumalvalavan, Murugesan
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 6, Pp 1320-1330 (2020)
In this study, we aimed to measure glomerular filtration rate (mGFR) using 99Tc DTPA in patients with Child-Pugh C cirrhosis and normal serum creatinine levels; and to compare the performance of creatinine and cystatin C-based equations [estimated GF
Externí odkaz:
https://doaj.org/article/43d2c1b574484d2ebc58c8f480bca9fd
Autor:
Remi George Thomas, R P Senthilkumar, Balaraman Velayudham, C Vasudevan, Thirumalvalavan Murugesan
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 3, Pp 676-680 (2020)
Classical Alport syndrome is a rare X-linked disease of males (85%) presenting early with hematuria, ocular, and hearing defects. Proteinuria and renal failure are less common in the early stages. Here, we report the case of a young female with nephr
Externí odkaz:
https://doaj.org/article/d611e0a26b83471f8cf756a2ac739216
Autor:
Murugesan, Balaraman Velayudham, R P Senthilkumar, Remi George Thomas, C Vasudevan, Thirumalvalavan
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 6, Pp 1320-1330 (2020)
In this study, we aimed to measure glomerular filtration rate (mGFR) using 99Tc DTPA in patients with Child-Pugh C cirrhosis and normal serum creatinine levels; and to compare the performance of creatinine and cystatin C-based equations [estimated GF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddfb4c52085c86cb5cc8ce4ac169f7da
http://www.sjkdt.org/article.asp?issn=1319-2442
http://www.sjkdt.org/article.asp?issn=1319-2442
Autor:
R P Senthilkumar, Remi George Thomas, C Vasudevan, Balaraman Velayudham, Thirumalvalavan Murugesan
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 3, Pp 676-680 (2020)
Classical Alport syndrome is a rare X-linked disease of males (85%) presenting early with hematuria, ocular, and hearing defects. Proteinuria and renal failure are less common in the early stages. Here, we report the case of a young female with nephr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fe04bc4f0846dfb48dbac9d0b40e161
http://www.sjkdt.org/article.asp?issn=1319-2442
http://www.sjkdt.org/article.asp?issn=1319-2442