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Research 211–240 of 320
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Value of dermoscopy for the diagnosis of monilethrix
- Early diagnosis of ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis syndrome: A case report
- Netherton Syndrome – Responding to Oral Retinoids
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Pioneers in Dermatology and Venereology: an interview with Professor Francisco Miguel Camacho Martinez
- Hypotrichosis in a child with olmsted syndrome
- Faculty Opinions recommendation of Loss of desmocollin 3 in mice leads to epidermal blistering.
- A case of dyschromatosis universalis
- Cell death by cornification
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Genetics of Inherited Ichthyoses and Related Diseases
- The genetics of alopecia areata: New approaches, new findings, new treatments
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Primary cicatricial alopecia: diagnosis and treatment
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Advances in regenerative medicine-based approaches for skin regeneration and rejuvenation