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Research 211–240 of 386
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Genetic hair and nail disorders
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Congenital atrichia associated with situs inversus and mesocardia
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Connexin mutations in human disease
- An audit of dermatoses at Baqai Institute of Skin Diseases, Karachi
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- TRPV3 Ion Channel: From Gene to Pharmacology
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- A 26-year-old man presenting with loss of vision, skin lesions and wasting
- Erythroderma, Alopecia, Anhidrosis, and Vitiligo as Complications of a Red Ink Tattoo—A Case Report
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Cutaneous manifestations of hypothyroidism: An observational study in a tertiary care center of Eastern India
- “Degeneration” in Dermatopathology
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Pioneers in Dermatology and Venereology: An Interview with Professor Danilo V. Stevanovic