Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Syed Nayer Mahmud"'
Autor:
Nadia Kareem, Chaudhary Muhamamd Juniad Nazar, Syed Nayer Mahmud, Armughan Ahmed, Muhammad Hammad Akhtar
Publikováno v:
Journal of Nephropharmacology, Vol 6, Iss 1, Pp 17-18 (2017)
Externí odkaz:
https://doaj.org/article/911a64d7f1fa4cadbe0e85f364de90c9
Publikováno v:
Pakistan Journal of Kidney Diseases. 6:26-33
Background: Hemodialysis has been shown to increase protein catabolism and led to significant loss of proteins during hemodialysis. Hypoalbuminemia has been associated with adverse outcomes. Therefore, the main aim of this study is to determine the e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c38f4577897e22b1288c68c3a271f2a
https://doi.org/10.53778/pjkd64192
https://doi.org/10.53778/pjkd64192
Publikováno v:
American Journal of Medical Case Reports. 9:725-729
We report a case of an elderly male patient, who presented with acute kidney injury on background of diabetic nephropathy, secondary to dapagliflozin induced acute tubulo-interstitial nephritis requiring hemodialysis sessions. Histopathological findi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4dbdfd197d2192b62fdd4c69f74a2a32
https://doi.org/10.12691/ajmcr-9-12-17
https://doi.org/10.12691/ajmcr-9-12-17
Publikováno v:
American Journal of Medical Case Reports. 10:183-185
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb200002ec197537daadd9fc86a2ae01
https://doi.org/10.12691/ajmcr-10-6-6
https://doi.org/10.12691/ajmcr-10-6-6
Publikováno v:
American Journal of Medical Case Reports. 9:693-697
Karyomegalic interstitial nephritis (KIN) is a rare cause of hereditary interstitial nephritis, described 45 years ago. Only about 50 cases have been described in English literature so far and none from Pakistan. This disease has an escalated course
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10e1d2783303cc677db297325136e716
https://doi.org/10.12691/ajmcr-9-12-8
https://doi.org/10.12691/ajmcr-9-12-8
Publikováno v:
Annals of Transplantation. 27
BACKGROUND Renal transplant recipients are susceptible to increased mortality with COVID-19 infection. There is insufficient data regarding risk factors for COVID-19 disease acquisition. We aimed to identify them here. MATERIAL AND METHODS We enrolle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d439cfe5398d3157ed01e529a0b94585
https://doi.org/10.12659/aot.937688
https://doi.org/10.12659/aot.937688
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72c54d41ddb6d5a04bec5ae56afafa3d
https://doi.org/10.7759/cureus.23149
https://doi.org/10.7759/cureus.23149
Publikováno v:
Cureus
Background Membranous nephropathy (MN) and immunoglobulin A nephropathy (IgAN) are although two different entities, yet can rarely coexist. There is not much data available on this coexistent disorder, specifically with regard to the treatment modali
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8da76754cd36f770958663875b83d7b5
https://pubmed.ncbi.nlm.nih.gov/34667681
https://pubmed.ncbi.nlm.nih.gov/34667681
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 32(7)
This study aimed to determine the percentage of anti-phospholipase A2 receptor (PLA2R) autoantibody positivity in a cross-section of 74 Pakistani patients with biopsy-proven idiopathic membranous nephropathy. It was an observational study conducted f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fed760d4965bbf7003289810ab9257b
https://pubmed.ncbi.nlm.nih.gov/35795953
https://pubmed.ncbi.nlm.nih.gov/35795953
Autor:
Syed Waqar Hussain, Syed Nayer Mahmud, Muhammad Luqman Saeed, Muhammad Tariq Khan, Zahid Siddique Shad, Muhammad Shoaib Safdar Qureshi, Azmat Abdullah, Kamran Munawar, Aayesha Qadeer, Behzad Kaleem Baloch
Publikováno v:
Cureus
Objective The goal of the study was to see if anti-ganglioside antibodies have a role in the diagnosis of Guillain-Barre syndrome (GBS). Study design Between May 2016 to October 2017, we conducted a prospective pilot study of 15 patients with a clini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4761e7ba76ee2919cb931e1af91107a2
https://pubmed.ncbi.nlm.nih.gov/31312551
https://pubmed.ncbi.nlm.nih.gov/31312551