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Research 271–300 of 1000+
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Interaction between stem cell factor and endothelin-1: effects on melanogenesis in human skin xenografts
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- The evolution of healthy skin to acne lesions: a longitudinal, <i>in vivo</i> evaluation with reflectance confocal microscopy and optical coherence tomography
- Superficial temporal artery flap for reconstruction of complex facial defects: A new algorithm
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Potential Medical Uses of Cannabigerol: A Brief Overview
- Management of hair loss diseases
- Exploring the Multifaceted Impact of Acne on Quality of Life and Well-Being
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice
- Biotinidase deficiency characterized by skin and hair findings
- Innovative Therapeutics in Pediatric Dermatology
- Iron and hair loss in women; what is deficiency? This is the real question!
- Prevalence Study of Dermatologic Manifestations among Diabetic Patients
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Use of Minced Residual Skin Grafts to Improve Donor Site Healing in Split-Thickness Skin Grafting
- Ectopic Sebaceous Glands in the Hair Follicle Matrix: Case Reports and Literature Review of this Embryogenic Anomaly
- 4-O-Methylhonokiol: A lesser-known neolignan from Magnolia species with diverse and promising pharmacological properties
- Inherited Disorders of the Hair
- Syndrome des ovaires polykystiques : Point de vue contemporain
- Microstructure of Defective Mink Guard Hair
- Eosinophilia associated with clozapine – A case report
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- Successful Management of Trichotillomania with an Integrated Approach: A Case Study
- Polycystic Ovary Syndrome: A Comprehensive Review of Its Clinical Presentation, Comorbidities, Long-Term Complications and Management
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Telogen Effluvium, Diagnosis and Management: A Narrative Review
- Rheumatoid arthritis and gouty arthritis in an adult patient with Down's syndrome
- Phylloid terminal hair nevus: A unique clinical entity
- Controversies in Polycystic Ovary Syndrome