Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Srinivasan Arivazhagan"'
Autor:
Dhanasekaran Rajasekar, Jayachandran Dhanapriya, Thanigachalam Dineshkumar, Ramanathan Sakthirajan, Thopalan Balasubramaniyan, Natarajan Gopalakrishnan, Srinivasan Arivazhagan
Publikováno v:
Indian Journal of Transplantation, Vol 12, Iss 3, Pp 182-186 (2018)
Background: Posttransplant erythrocytosis (PTE) is defined as persistently elevated hemoglobin (Hb) >17 g/dl and or PCV >51% in renal transplant recipients. The incidence of PTE varies from 8% to 22%, with occasional life-threating thromboembolic com
Externí odkaz:
https://doaj.org/article/a98cc6ddc6694c30ae0155fcf258ff5e
Autor:
Srinivasan Arivazhagan, Tanuj Moses Lamech, Murugan Myvizhiselvi, Venkatesh Arumugam, Sheik Sulthan Alavudeen, Shivakumar Dakshinamoorthy, Thanigachalam Dineshkumar, Ramanathan Sakthirajan, Jeyachandran Dhanapriya, Palaniselvam Shankar, Rajendran Padmaraj, Anila Abraham Kurien, Natarajan Gopalakrishnan
Publikováno v:
Kidney international reports. 7(10)
Infection-related glomerulonephritis (IRGN) is associated with glomerular immune complex deposition along with complement activation. Steroids may attenuate glomerular injury and thereby improve renal outcomes.We randomly assigned patients who had bi
Autor:
R Sakthirajan, Thopalan Balasubramaniyan, T Dineshkumar, Jayachandran Dhanapriya, Srinivasan Arivazhagan, Natarajan Gopalakrishnan, Dhanasekaran Rajasekar
Publikováno v:
Indian Journal of Transplantation, Vol 12, Iss 3, Pp 182-186 (2018)
Background: Posttransplant erythrocytosis (PTE) is defined as persistently elevated hemoglobin (Hb) >17 g/dl and or PCV >51% in renal transplant recipients. The incidence of PTE varies from 8% to 22%, with occasional life-threating thromboembolic com
Autor:
Thanigachalam Dineshkumar, Ramanathan Sakthirajan, Arcot Thanjan Maasila, Srinivasan Arivazhagan, Natarajan Gopalakrishnan, Jeyachandran Dhanapriya, T Balasubramaniyan, Dhanasekaran Rajasekar
Publikováno v:
Journal of Integrative Nephrology and Andrology. 4:26
Anti-glomerular basement membrane (anti-GBM) disease is an autoimmune disorder characterized by crescentic glomerulonephritis, pulmonary hemorrhage, and the presence of circulating anti-GBM antibodies which bind to the α3 chain of Type IV collagen f