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Research 31–60 of 1000+
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Secondary cicatricial and other permanent alopecias
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- The Spectrum of Skin Disease Among Indian Children
- Darier Sign: A Historical Note
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Bad Hair Days: A Clinical and Trichoscopic Evaluation of Scalp Lesions
- The Genetics of Human Skin Disease
- The spectrum of nephrocutaneous diseases and associations
- Graft-versus-host disease
- Description of skin lesions
- Skin signs of systemic diseases
- Ichthyosis hystrix
- Disorders of Keratinization
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- “Degeneration” in Dermatopathology
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Poster Presentations
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Off-label uses of retinoids in dermatology
- Chronic graft versus host disease and skin
- Vitamin D and skin diseases: A review
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Trichoscopy in genetic hair shaft abnormalities
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex