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Research 391–420 of 978
- TRP Channels in Skin Biology and Pathophysiology
- Targeting integrin pathways: mechanisms and advances in therapy
- Furnishing Wound Repair by the Subcutaneous Fascia
- Pain in Multiple Sclerosis: Understanding Pathophysiology, Diagnosis, and Management Through Clinical Vignettes
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- Novel Therapeutic Hybrid Systems Using Hydrogels and Nanotechnology: A Focus on Nanoemulgels for the Treatment of Skin Diseases
- Prevention and Treatment of Chemotherapy-Induced Alopecia
- Micro-autologous Fat Transplantation (MAFT) for Forehead Volumizing and Contouring
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Advances in single-cell transcriptomics in animal research
- Skin Development and Disease: A Molecular Perspective
- Lithium: one drug, five complications
- Men’s health in the United States: a national health paradox
- Lateral oblique forehead lines: redefining sleeping lines and treatment with botulinum toxin A
- Protective Efficacy of Vitamin F against Acrylamide Induced Toxicity: Studies on Oxidative Stress Biomarkers
- Impacts of Anabolic-androgenic steroid supplementation on female health and offspring: Mechanisms, side effects, and medical perspectives
- Efectos adversos asociados al uso de anabolizantes en deportistas: revisión sistemática
- Advanced Lipotransfer Techniques
- Skin development in the gray short‐tailed opossum (<i>Monodelphis domestica</i>)—From skin respiration to thermoregulation
- Dose-Response Relationship of Therapeutic Oxygen: More Is Not Necessarily Better and May Be Inferior to No Supplemental Oxygen – Part 2: Implications and Consequences
- E-Poster
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism
- The impact of healthcare setting on post-COVID mood disorders: a single-centre perspective from Southern Italy Respiratory Intensive Care Unit
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Muscular Increase and Definition of the Back Contour Through Key Fat Grafting and Liposuction
- 494 Epidermolysis bullosa pruriginosa, muscular dystrophy, and immune-mediated myasthenia gravis in a patient with homozygous nonsense PLEC mutation
- Corticosteroids for the treatment of Duchenne muscular dystrophy
- G.P.2.16 Valproate, acetylcarnitine, folic acid and vitamin B12 in spinal muscular atrophy: Preliminary data of an open-label study in children
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat