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Research 31–60 of 786
- Sjogren-Larsson Syndrome
- FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures
- Uso actual de la vitamina D en dermatología
- Genetics
- Mykogene und piläre Faktoren des Haarabbaus durch Dermatomyzeten* (2. Mitteilung)
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Ichthyosis with confetti: clinics, molecular genetics and management
- Oral Retinoids in Dermatology
- Inherited Disorders of Corneocyte Proteins
- Disorders of Keratinization
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Dermatological diseases from a genetic perspective
- Postgraduate seminar in pediatric dermatology
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- New developments in the molecular treatment of ichthyosis: review of the literature
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Quoi de neuf en dermatologie pédiatrique ?
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- Novel Drugs Targeting Retinoic Acid Receptors
- Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition
- Oral retinoids-present status
- From molecular biology to therapeutics
- Skin Manifestations of Hypothyroidism-A Clinical Study
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide