Results 181 to 190 of about 189,380 (263)
Microglia-vascular interactions after spinal cord injury: regulatory mechanisms and therapeutic advances. [PDF]
Zhao Y +8 more
europepmc +1 more source
Otogenic route of meningitis was associated with greater cochlear hair cell loss in comparison with the meningogenic one in this otopathology study. Neuronal depletion has been traditionally implicated in failed hearing rehabilitation of post‐meningitis deafness.
Matheus Pedrosa Tavares +5 more
wiley +1 more source
Spinal cord injury induces acute microbiome shock and system-wide transcriptomic reprogramming. [PDF]
Zhang C +10 more
europepmc +1 more source
National Trends and Risk Factors for Dysphagia After Anterior Cervical Discectomy and Fusion
From 2016 to 2023, inpatient anterior cervical discectomy and fusion (ACDF) volume declined 52.2% while postoperative dysphagia rates increased 11.4% annually. Analysis of 496,425 cases demonstrated that dysphagia risk varied markedly by surgical indication, with cervical diffuse idiopathic skeletal hyperostosis, cervical spine fracture, and ...
Caryn J. Ha +4 more
wiley +1 more source
Exosomes as regenerative therapeutics for spinal cord injury: mechanisms and clinical prospects. [PDF]
Xiao Y, Cui T, Zhou Y, Su Q, Yi D.
europepmc +1 more source
Polymerized Pro‐Estrogen Microneedles via Two Photon Polymerization
Acrylic pro‐drugs of 17β‐estradiol were subjected to spatially controlled two‐photon polymerization to create bespoke microneedle geometries with potential biomedical applications for long‐term transdermal hormone delivery. ABSTRACT Two‐photon polymerization (TPP) is a powerful technique to create microscale structures with high precision, offering ...
Yang Lou +6 more
wiley +1 more source
Rewiring the Lung-CNS Axis After Spinal Cord Injury. [PDF]
Wu H +6 more
europepmc +1 more source
Quality of life after spinal cord injury: a qualitative interview-based study. [PDF]
Stenimahitis V +7 more
europepmc +1 more source
Abstract Background Variants in AFG3‐Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous variant and one family with inherited heterozygous variant in AFG3L2 gene.
Sangeetha Yoganathan +14 more
wiley +1 more source

