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Research 451–480 of 1000+
- A Rare Case of Cutis Verticis Gyrata with Underlying Cerebriform Intradermal Nevus
- Dental considerations in acrodermatitis enteropathica: A report of two cases
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Cutaneous gene therapy
- A case of unilateral congenital triangular alopecia
- Trichohyalin is a Potential Major Autoantigen in Human Alopecia Areata
- Exploring Pediatric Dermatology in Skin of Color: Focus on Dermoscopy
- Cutaneous Side Effects of Modern Targeted Therapy and Immunotherapy in Patients with Dermatological Malignancies
- Ethnopharmacological Significance of <i>Eclipta alba</i> (L.) Hassk. (Asteraceae)
- Recurrent furunculosis – challenges and management: a review
- Selenium Compounds and Their Bioactivities: Molecular Mechanisms and Prospects for Functional Food and Therapeutic Applications
- Off-label uses of retinoids in dermatology
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- [Cutaneous manifestations of malabsorption diseases (author's transl)].
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- IMPORTANCE OF ISOLATED GESTATIONAL HYPOTHYROXINEMIA IN THE DEVELOPMENT OF OBSTETRIC AND SOMATIC PATHOLOGIES.
- Zinc-responsive Acral Hyperkeratosis as a Sequele of Acrodermatitis Enteropathica
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Developmental signals in skin morphogenesis
- Trichoscopy in alopecias: Diagnosis simplified
- PKC downregulation upon rapamycin treatment attenuates mitochondrial disease
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Cellular senescence in skin‐related research: Targeted signaling pathways and naturally occurring therapeutic agents
- Ophthalmologic Comorbidities in Alopecia Areata
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Homeostatic Control of Sebaceous Glands by Innate Lymphoid Cells Regulates Commensal Bacteria Equilibrium
- Mineral Malnutrition Following Bariatric Surgery
- A Systematic Review of Persistent Symptoms and Residual Abnormal Functioning following Acute COVID-19: Ongoing Symptomatic Phase vs. Post-COVID-19 Syndrome
- Epidermal Wnt/β-catenin signaling regulates adipocyte differentiation via secretion of adipogenic factors