Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Suman Sethi"'
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 34, Iss 1, Pp 80-83 (2023)
Sporotrichosis is a rare form of subacute and chronic fungal infection in renal transplant recipients caused by the ubiquitous fungus Sporothrix schenckii. It is usually described in renal allograft recipients who have not been treated with antifunga
Externí odkaz:
https://doaj.org/article/258d2cd4dc9b48e498e5a798b2d39915
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 34, Iss 3, Pp 224-234 (2023)
In recent years, adynamic bone disease (ABD) has become a common skeletal lesion in adult patients with chronic kidney disease. We aimed to compare the effects of low calcium dialysate (LCD) and standard calcium dialysate of our facility [high calciu
Externí odkaz:
https://doaj.org/article/3810954288ee47acaeba7a5daf03a4d2
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 33, Iss 4, Pp 559-565 (2022)
Nutritional assessment is a basic and necessary process in the nutritional management of dialysis patients. Malnutrition is a prevalent complication in patients on maintenance hemodialysis (HD). The study aimed to evaluate its relationship with the d
Externí odkaz:
https://doaj.org/article/a0703b79622642e38a93955c26c65218
Autor:
Vivek Gupta, Samir Kapoor, Vikas Makkar, Shibba Takkar Chhabra, Naved Aslam, Bishav Mohan, Rajiv Kumar, Vijita Pandey, Himani Prashar, Gurkirat Kaur, Suvir Grover, Suman Sethi, Simran Kaur, Sarju Ralhan, G.S. Wander
Publikováno v:
Indian Heart Journal, Vol 73, Iss 5, Pp 594-598 (2021)
Background: Clinical experience on details of CRRT initiation and outcomes in cardiac intensive care unit (CICU) patients is not available from developing countries like India. This study shares the 5-year clinical experience of managing CICU patient
Externí odkaz:
https://doaj.org/article/e4ec8d31224245bd89c3b0712897ec17
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 32, Iss 5, Pp 1461-1464 (2021)
Xanthogranulomatous pyelonephritis (XGPN) is an uncommon chronic destructive granulomatous inflammation of the kidney with variable clinical and radiological presentation. Due to its similarities to other benign and malignant pathologies, a high inde
Externí odkaz:
https://doaj.org/article/5281f4fe3a1e4f36a405dd8fd6948144
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 32, Iss 3, Pp 865-868 (2021)
After its discovery in Wuhan, China, in December 2019, coronavirus disease 2019 (COVID-19) has now become a pandemic in a short period. The kidney involvement is frequently reported, especially in critically ill hospitalized patients. Multiple mechan
Externí odkaz:
https://doaj.org/article/7b00003013164a19899f1d889f621d17
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 31, Iss 1, Pp 285-288 (2020)
The oculocerebrorenal (OCRL) syndrome, also known as Lowe syndrome (LS), is an X-linked recessive disorder that predominantly affects males and is characterized by growth and mental retardation, congenital cataract and renal Fanconi syndrome. OCRL1 i
Externí odkaz:
https://doaj.org/article/d918aa68bdad4a5eb486b9b2b6fac582
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 5, Pp 1171-1174 (2019)
Hematological conditions rarely present as isolated hematuria. Factor VII deficiency is a rare congenital coagulopathy inherited as autosomal recessive pattern. It usually presents a severe life-threatening bleeding at an early age. The presentation
Externí odkaz:
https://doaj.org/article/752138730ac24530a0a85e791486a916
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 4, Pp 969-973 (2019)
Metachondromatosis is a rare disorder of autosomal inheritance with incomplete penetrance, which is characterized by formation of osteochondroma and enchondroma, caused by loss of function of the protein tyrosine phosphatase nonreceptor type 11 (PTPN
Externí odkaz:
https://doaj.org/article/422a22246b134523ae06a8f01e67b470
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 30, Iss 4, Pp 978-981 (2019)
Melanonychia is described as a brown to black pigmentation of nail, due to stimulation and hyperplasia of nail matrix. Various systemic disorders, trauma, inflammatory disorders, fungal infections, drugs, benign melanocytic hyperplasia, etc., are res
Externí odkaz:
https://doaj.org/article/c9df7ce3d2f447278ec71e93f9049354