Results 161 to 170 of about 801,284 (359)
Background and Objectives: To evaluate the surgical outcomes of intraocular lens (IOL) refixation with vitrectomy in patients with elevated intraocular pressure (IOP) due to IOL subluxation.
Kentaro Iwasaki+4 more
doaj +1 more source
A novel, non‐enzymatic electrochemical sensor employing gold‐copper nano‐brambles enables rapid, accurate, and chloride‐tolerant chemical oxygen demand (COD) detection. Demonstrating high sensitivity and excellent performance in real wastewater samples, this portable platform offers a sustainable and efficient alternative for on‐site COD monitoring in ...
Federica Simonetti+8 more
wiley +1 more source
910. Gene Therapy of Glycogenosis Type 2Using SIN-Lentiviral Vectors [PDF]
Emmanuel Richard+4 more
openalex +1 more source
Crystallographic study of mixture Ba 0.6 Nd 0.4 CuO y , in the range of annealing temperatures 860 o - 910 o C [PDF]
A powder mixture of BaCO3, Nd2O3 and CuO was prepared according to the chemical formula Ba0.6Nd0.4CuOy. The mixture was heated successively for several hours (52 to 75h) in free atmosphere at temperatures 860 oC, 870 oC, 880 oC, 890 oC, 900 oC and 910 oC.
Danis Kerasiotis (1247337)
core
Vascular Necrosis Caused by Application of Methyl 2-Cyanoacrylate (Eastman 910 Monomer)
Robert H. Goetz+2 more
openalex +2 more sources
The Use of a Polyglactin 910 Mesh to Obtain Haemostasis and Prevent Further Splitting in a Fractured Transplant Kidney [PDF]
R Gandy+4 more
openalex +1 more source
Steroid photoreactivity was a major topic in the last century. This study revisits it by exploring the photochemistry of Δ1‐keto‐steroids, offering an efficient method to modify the classic steroid 6/6/6/5 ring system. This approach enables the transformation of accessible steroids into rare ones, demonstrated by synthesizing 5,6‐dihydro‐ophiopogonol A
Chiara Maioli+8 more
wiley +1 more source
Rett syndrome (RTT) is a severe X-linked neurodevelopmental disorder that is primarily caused by mutations in the methyl CpG binding protein 2 gene (MECP2). RTT is the second most prevalent cause of intellectual disability in girls and there is currently
Valerie Matagne+7 more
doaj