Search
for
Sort by
Research 91–120 of 1000+
- Ichthyosis linearis circumflexa with bamboo hair: challenges in the diagnosis and management
- Side effects of mesotherapy - review
- Tissue Engineering of the Reproductive System
- Hidradenitis Suppurativa: From Physiopathologies to Targeted Therapeutics
- Covas-Lift: Facial Enhancement
- Surgical Anatomy of the Scalp
- Forehead, Eyebrow, and Upper Eyelid Lifting
- Psoriatic scarring alopecia
- Disease modifying agent related skin reactions in multiple sclerosis: prevention, assessment, and management
- Dermatologische Probleme bei Kindern mit Adipositas
- Platelet-Rich Plasma and Acellular Dermal Matrix in the Surgical Treatment of Hidradenitis Suppurativa: A Comparative Retrospective Study
- Inborn Errors of Biotin Metabolism
- PHYSICALLY INDUCED PEMPHIGUS AFTER COSMETIC PROCEDURES
- Leave the Fat, Skip the Bolster: Thinking outside the Box in Lower Third Nasal Reconstruction
- Surgical Anatomy of the Scalp
- Superficial temporal artery flap for reconstruction of complex facial defects: A new algorithm
- Cutaneous changes in patients with chronic renal failure on hemodialysis
- Lucio Phenomenon: Sequelae of Neglected Leprosy
- Transtemporal Midface Lifting to Blend the Lower Eyelid-Cheek Junction
- Techniques for Rejuvenation of the Neck Platysma
- Algorithm of Hair Restoration Surgery in Children
- Inborn errors of biotin metabolism
- A case of erosive pustular dermatosis of the scalp in a pediatric patient
- The Facelift
- Immune reconstitution inflammatory syndrome associated with secondary syphilis: dermatologic, neurologic and ophthalmologic compromise in an HIV patient
- Dermatologic Conditions of the Early Post-Transplant Period in Hematopoietic Stem Cell Transplant Recipients
- Polycystic Ovary Syndrome (PCOS): From Diagnosis to Treatment
- Epigenetic orchestration of RNA m<sup>6</sup>A methylation in wound healing and post-wound events
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn