• A <em>Dpagt1</em> Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in Mice
• A clinical case of a growing patient with juvenile rheumatoid arthritis of the temporomandibular joint
• A Dpagt1 Missense Variant Causes Degenerative Retinopathy without Myasthenic Syndrome in Mice
• Developing Cell-Based Therapies for RPE-Associated Degenerative Eye Diseases
• Evaluation of neurodegenerative and inflammatory processes in temporomandibular joint disorders using optical coherence tomography
• Human ESC-derived retinal epithelial cell sheets potentiate rescue of photoreceptor cell loss in rats with retinal degeneration
• Hydroxy group requirement for halofuginone-dependent inhibition of muscle fibrosis and improvement of histopathology in the mdx mouse model for Duchenne muscular dystrophy
• Imaging of psoriatic arthritis and aspects of radiographic progression
• Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination
• Myofibrillar Lattice Remodeling Is a Structural Cytoskeletal Predictor of Diaphragm Muscle Weakness in a Fibrotic <em>mdx</em> (<em>mdx Cmah^-/-</em>) Model
• Neurological symptoms and disorders following electrical injury: A register-based matched cohort study
• Next-generation mapping: a novel approach for detection of pathogenic structural variants with a potential utility in clinical diagnosis
• Regeneration from three cellular sources and ectopic mini-retina formation upon neurotoxic retinal degeneration in Xenopus
• Surgical Technique for Pulled in Two Syndrome: Three Cases With Chronic Progressive External Ophthalmoplegia
• The idebenone metabolite QS10 restores electron transfer in complex I and coenzyme Q defects
• Toxicological Characterization of Exon Skipping Phosphorodiamidate Morpholino Oligomers (PMOs) in Non-human Primates
• Variants within the SP110 nuclear body protein modify risk of canine degenerative myelopathy