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Research 781–810 of 789
- Chemically Induced Depigmentation of Skin and Hair
- Protein profiling of forehead epidermal corneocytes distinguishes frontal fibrosing from androgenetic alopecia
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Suppression of Vitamin D Receptor and Induction of Retinoid X Receptor α Expression During Squamous Differentiation of Cultured Keratinocytes
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Hyperpigmentation Associated with the Use of Topical Cidofovir for Treatment of Trichodysplasia Spinulosa in an Immunosuppressed Adult: Case Report and Review of the Literature
- Mind–Body Integrative Treatment of Psychodermatoses
- Hypothesis: platelet-rich plasma as an adjunct therapy for eczema targeting inflammation, skin barrier repair, and chronic recurrence
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Dental Management in a 7-year-old Child with Ichthyosis Vulgaris: A Rare Case Report
- Ichthyosis vulgaris involving the scalp area affected by androgenetic alopecia.
- Ichthyosis
- 155 Exploring perceived quality of life in middle- to old-aged patients with inherited ichthyosis: a qualitative study
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Dermatological aspects of the S2k guidelines on Down syndrome in childhood and adolescence
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Presentations of Cutaneous Disease in Various Skin Pigmentations: Keratosis Pilaris
- Keratosis Pilaris Is a Keratinization of Hair Follicles
- Disorders of Keratinization
- Genetics
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Viva questions from the IJDVL
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- The value of trichoscopy in the differential diagnosis of scalp lesions in pemphigus vulgaris and pemphigus foliaceus
- Management of congenital ichthyoses: European guidelines of care, part two
- NETHERTON'S SYNDROME AND ICHTHYOSIS LINEARIS CIRCUMFLEXA
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- 0952 Spatial transcriptomics reveal compartmentalized dysregulation of lipid metabolism in acne vulgaris