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Research 991–1000 of 1000+
- A missense mutation in Lama3 causes androgen alopecia
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports