Zobrazeno 1 - 10
of 124
pro vyhledávání: '"M. Hussain"'
Autor:
Raafae M. Hussain
Publikováno v:
The Journal of Foot and Ankle Surgery. 60:634-641
Total talar replacement is a viable treatment option for talar injuries and pathologies. We present a single case study of a 73-year-old female with idiopathic necrosis of the talar which was treated with a total talar replacement prosthesis. A patie
Publikováno v:
Hand (N Y)
Background Proximal interphalangeal joint (PIPJ) arthrodesis can provide reliable pain relief and restore hand function in patients with PIPJ arthritis. However, there is a paucity of literature on patient-specific preoperative risk factors that are
Publikováno v:
British Journal of Surgery. 108
Aim To evaluate the primary anatomical success and visual outcomes in patients with rhegmatogenous retinal detachment (RRD) undergoing 25-gauge pars plana vitrectomy (25g PPV) surgery in Pakistan. Method This is a five-year retrospective, interventio
Autor:
Evan A. Scott, Sharan Bobbala, Baixue Xiao, Sean D. Allen, Matthew DeBerge, Edward B. Thorp, Cameron L. Braverman, Peter I. Hecker, Sijia Yi, Xiaohan Zhang, Lei Cai, Samuel I. Stupp, Ryan E. Temel, Yugang Liu, M. Hussain Sangji
Publikováno v:
Adv Funct Mater
The principle cause of cardiovascular disease (CVD) is atherosclerosis, a chronic inflammatory condition characterized by immunologically complex fatty lesions within the intima of arterial vessel walls. Dendritic cells (DCs) are key regulators of at
Autor:
A. Corona, S. M. Jain, E. Luvsannyam, N. Ullah, M. Abbas, T. M. Hussain, Arathi Jayaraman, R. Zhuleku, A. N. Siddiqui
Publikováno v:
Cureus
Acute limb ischemia (ALI) is the sudden decrease in limb perfusion caused by embolism secondary to many blood stasis conditions. Treatment commences with intravenous (IV) unfractionated heparin infusion. Individuals can have an immune-mediated reacti
Publikováno v:
Ophthalmic Surgery, Lasers and Imaging Retina. 50:661-663
Leber's congenital amaurosis (LCA) is a rare inherited retinal degeneration (IRD) that causes severe vision loss, nyctalopia, and nystagmus within the first few years of life. RPE65 gene mutations cause approximately 6% of LCA cases and have become t
Autor:
Harry W. Flynn, Ninel Z. Gregori, Thomas A. Ciulla, Audina M. Berrocal, Rehan M. Hussain, Byron L. Lam
Publikováno v:
Expert Opinion on Biological Therapy. 18:1049-1059
Stargardt macular dystrophy (STGD1) is a hereditary retinal degeneration that lacks effective treatment options. Gene therapy, stem cell therapy, and pharmacotherapy with visual cycle modulators (VCMs) and complement inhibitors are discussed as poten
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 31(10)
The natural history of benign enlargement of the prostate is variable and ranges from mild symptoms to chronic retention and renal failure. In this study, the outcomes of patients with urinary retention alone were compared with those of chronic reten
Publikováno v:
Indian Journal of Forensic Medicine & Toxicology.
The current study aimed to evaluate the mechanism of reducing the effect of (RA) after it was induced inmale white rat with a Complete Freund’s Adjuvant (CFA) at TNF-? level by treating Xerogel Nanoparticlesand dexamethasone nanocompounded (Xerogel
Publikováno v:
Expert opinion on biological therapy. 20(9)
The development of intravitreal anti-vascular endothelial growth factor (VEGF) therapy has revolutionized management of neovascular age-related macular degeneration (nAMD) and serves as the standard of care for treating this chronic, progressive dise