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Research 331–360 of 645
- The role of PEDF in ageing and development: reduction of oxidative damage and support for stem cells
- Serotonin activates dermal papilla cells and promotes hair growth
- Commonly encountered symptoms and their management in patients with cirrhosis
- Pharmacotherapy for Keloids and Hypertrophic Scars
- Melanocytes in regenerative medicine applications and disease modeling
- HDAC6-dependent deacetylation of NGF dictates its ubiquitination and maintains primordial follicle dormancy
- Treatment of Androgenetic Alopecia: Current Guidance and Unmet Needs
- Table of Contents
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Referee report. For: Pathogenesis of Androgenetic alopecia [v1; indexed, http://f1000r.es/5ar]
- Highlights from the Literature
- Testosterone metabolites differentially maintain adult morphology in a sexually dimorphic neuromuscular system
- PROSTATITIS, A NEUROMUSCULAR DISORDER: ITS CAUSES, SYMPTOMS, DIAGNOSIS, AND MANAGEMENT
- Surgical Treatment of the Brow and Upper Eyelid
- Comprehensive Management of Eyebrow and Forehead Ptosis
- Leprosy on the scalp
- Tourniquet syndrome in children (literature review and own observation)
- Hair transplantation
- Scalp Surgery
- Recipient Site Anesthesia and Hemostasis
- Cosmetic Treatment Using Botulinum Toxin in the Oral and Maxillofacial Area: A Narrative Review of Esthetic Techniques
- Ptosis in childhood
- Botulinum toxin in modern clinical and aesthetic medicine: history, applications, risks and future perspectives
- Regeneration of Peripheral Nerves Using Neuroinductive Biomaterial Scaffolds
- Scalp Surgery: Anatomic and Biomechanical Considerations
- Chronic inflammatory demyelinating polyneuropathy associated with alopecia totalis and Sjögren syndrome
- Rethinking biotin therapy for hair, nail, and skin disorders
- Use of Verteporfin with Dermal Wounding to Regenerate New Hair in Androgenetic Alopecia
- Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications
- 307 Phenotypic-genotypic expansion of plectinopathy in a patient with muscular dystrophy and immune-mediated myasthenia gravis