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Research 61–90 of 160
- <i>Malassezia</i> and the Asian menopausal skin
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Hair Loss in Children
- Disorders of hair in children
- Dermatophytosis in companion animals: A review
- Wnt signaling: the good and the bad
- Stem Cell-Based Tissue Engineering for the Treatment of Burn Wounds: A Systematic Review of Preclinical Studies
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- Restoration of hair-inductive activity of cultured human follicular keratinocytes by co-culturing with dermal papilla cells
- Geriatric Dermatologic Therapy
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Dermatological Maifestations of Obesity
- The role of zinc deficiency in the pathogenesis of dermatoses
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- 565 Cutaneous delivery of LEKTI via an engineered strain of staphylococcus epidermidis for the treatment of netherton syndrome
- Vulvovaginal involvement in Netherton syndrome: A case report
- Érythrodermies néonatales et infantiles : apport de la biopsie cutanée précoce dans les formes graves
- Efficacy of Dupilumab in Treating Atopic Dermatitis With Recurrent Eczema Herpeticum in a Patient With DOCK8-Deficiency Hyper-IgE Syndrome: A Case Report
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- Genetic Hair Disorders: A Review
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy.
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Trichorrhexis Invaginata and Netherton’s Syndrome
- ESDR303 – The role of rare variants in male-pattern hair loss: Analysis of whole exome sequencing data in the UK Biobank