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Research 361–390 of 1000+
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Dissecting Cellulitis of the Scalp: Linking Pathogenesis to Therapy
- Linear Lichen Planopilaris of the Trunk: First Report of a Case
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Diagnostic Value of DermoscopicFindings of Hair and Scalp in Cicatricial Alopecia
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Cicatricial Alopecia
- The spectrum of fibrosing alopecias
- Eruptive vellus hair cyst: An uncommon and underdiagnosed entity
- Erosive Pustular Dermatosis: Delving into Etiopathogenesis and Management
- Current Genetics in Hair Diseases
- Bachmann–Bupp syndrome and treatment
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Quality of life in children with scalp hair loss: a Clinico-epidemiological study
- Alopecia Areata: Pathogenesis, Diagnosis, and Therapies
- Pathophysiology and Nutritional Approaches in Polycystic Ovary Syndrome (PCOS): A Comprehensive Review
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Primary cicatricial alopecia: diagnosis and treatment
- Trichoscopy in genetic hair shaft abnormalities
- Off-label uses of retinoids in dermatology
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Approach to Nail Pitting in Pediatric and Adolescent Patients: A Dermatology Perspective
- Prostaglandin F2α stimulates the growth of human intermediate hair follicles in ex vivo organ culture with potential clinical relevance
- Epidermal Nevi
- In Vivo Imaging Techniques for the Human Scalp: A Systematic Review of the Literature
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Focal alopecia in parietal area in adult women — assessment of usefulness of trichoscopy in making a proper diagnosis
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation