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Research 271–300 of 1000+
- Pityriasis rubra pilaris: A study evaluating patient quality of life in 2 populations
- Dermoscopic Findings and Their Therapeutic Implications in Trichostasis Spinulosa: A Retrospective Study of 306 Patients
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Lichen Spinulosus: Case Report and Review of Literatures
- Immunohistochemical expression of cytokeratin 15, cytokeratin 19, follistatin, and Bmi-1 in basal cell carcinoma
- Controversies in off‐label prescriptions in dermatology: the perspective of the patient, the physician, and the pharmaceutical companies
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Current concepts in the pathogenesis and treatment of acne
- A newborn presenting with congenital blistering
- Increasing Access to Specialized Dermatology Care: A Retrospective Study Investigating Clinical Operation and Impact of a University-Affiliated Free Clinic
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Diffuse scarring alopecia in a female pattern hair loss distribution
- Building Models for Keratin Disorders
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Erosive Pustular Dermatosis of the Scalp: Clinicopathological Correlation Leading to a Definition of Diagnostic Criteria.
- Chronic Crusted Scalp Lesion of an Elderly Male
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- Prevalência das lesôes cutâneas em Freixo de Espada à Cinta.
- Seborrheic karatosis, a tumor of the infundibular and isthmus of hair follicles: Identification of hair sheath keratins and histopathological features suggesting hair follicle origin.
- Teledermatology: An updated overview of clinical applications and reimbursement policies
- Ichthyosis fetalis in a cross‐bred lamb
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Ectodermal Dysplasia: Variable Expressions
- Androgenic Alopecia: A Comprehensive Literature Review of Epidemiology, Pathophysiology, Diagnosis, and Management
- Surgical Management of Severe Cicatricial Ectropion Secondary to Pityriasis Rubra Pilaris.
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Acquired and inheritedhair disorders