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Research 31–60 of 1000+
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Structural and biochemical changes underlying a keratoderma-like phenotype in mice lacking suprabasal AP1 transcription factor function
- Pattern of Skin disorders across age groups
- The Genetics of Human Skin Disease
- 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 Spectrum of Skin Disease Among Indian Children
- Description of skin lesions
- Oral retinoids-present status
- Dermatological Manifestations of Stress in Normal and Psychiatric Populations
- Oral Retinoids in Dermatology
- Skin signs of systemic diseases
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Disorders of Keratinization
- “Degeneration” in Dermatopathology
- Ichthyosis hystrix
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Poster Presentations
- Changing Patterns of Localization of Putative Stem Cells in Developing Human Hair Follicles
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- The molecular basis of human keratin disorders
- Off-label uses of retinoids in dermatology
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Trichoscopy in genetic hair shaft abnormalities
- Chronic graft versus host disease and skin
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture