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Research 61–90 of 1000+
- Dermatopathology and molecular genetics
- Intracorneal vacuoles in skin diseases with parakeratotic hyperkeratosis in the dog: a retrospective light‐microscopy study of 111 cases (1973–2000)
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Oral retinoids-present status
- Beyond Clinical Efficacy: A Literature Review on the Safety Challenges of Isotretinoin Therapy
- Comprehensive Administrative and Engineering Strategies for Radiation Protection and Occupational Health Safety
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- Ptosis in childhood
- Characterization of an autoimmune condition associated with AEC syndrome
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Schmallenberg virus infection suspected in a calf born to an imported heifer
- Genetics of Inherited Ichthyoses and Related Diseases
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Epidermis-specific ablation of claudin-1 in adult mice demonstrates the essential role of a tight junction barrier in skin homeostasis
- Cell Polarization Defects in Early Heart Development
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy