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Research 601–630 of 998
- The evolution of platelet-rich plasma: A 70-year-old history
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Fatal Case of Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Induced by Doxycycline or Flucloxacillin in a 77-Year-Old Woman: A Rare but Serious Adverse Drug Reaction
- Systematic Review of Platelet-Rich Plasma in Medical and Surgical Specialties: Quality, Evaluation, Evidence, and Enforcement
- THE USE OF PLATELET-RICH PLASMA IN THE TREATMENT OF ALOPECIA - A REVIEW OF THE LITERATURE
- A case study of using cross-linked hyaluronic acid for upper eyelid rejuvenation
- Updates From 2021 Virtual Dermatology Nurses' Association Convention
- Graham-Little Piccardi Lassueur Syndrome and review of the literature
- Autologous Platelet-Rich Plasma (PRP) for Treating Androgenetic Alopecia: A Novel Treatment Protocol Standardized on 2 Cases
- Development and evaluation of animal models for sex steroid deficient dry eye
- Parental Uveitis Influences Offspring With an Increased Susceptibility to the Experimental Autoimmune Uveitis
- Plasma rico en plaquetas como terapia autóloga en la medicina regenerativa: Revisión narrativa
- Pancytopenia in epidemic dropsy: a case report
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Patient factors influencing dermal filler complications: prevention, assessment, and treatment
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Frontiers in alopecia areata pathobiology research
- Morphea: progress to date and the road ahead
- Primary cicatricial alopecia: diagnosis and treatment
- Dermatologic care for lesbian, gay, bisexual, and transgender persons
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Lichen planopilaris and frontal fibrosing alopecia: review and update of diagnostic and therapeutic features
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Eyebrow and Eyelash Alopecia: A Clinical Review
- Cellular Senescence and Aging in Myotonic Dystrophy
- Seborrheic Dermatitis Revisited: Pathophysiology, Diagnosis, and Emerging Therapies—A Narrative Review
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- The Use of Imaging Techniques in the Diagnosis of Dermatoses of the Scalp