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Research 841–870 of 1000+
- Successful Treatment of Coexisting Alopecia Areata and Bullous Pemphigoid With Dupilumab: A Case Report
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Paradise Nut Paradox: Alopecia Due to Selenosis from a Nutritional Therapy
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Human hair keratin and its-based biomaterials for biomedical applications
- Central Centrifugal Cicatricial Alopecia Presenting with Irregular Patchy Alopecia on the Lateral and Posterior Scalp
- Male and female pattern hair loss: Treatable and worth treating
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Ichthyosis with confetti: clinics, molecular genetics and management
- Cure of alopecia areata after eradication of Helicobacter pylori: a new association?
- Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis
- Methylenetetrahydrofolate reductase C677T mutation in patients with alopecia areata in Turkish population
- Structure and expression of the ovine Hoxc-13 gene
- Topical corticosteroid in foam vehicle offers comparable coverage compared with traditional vehicles
- Refractory alopecia in lupus treated with tofacitinib — a case-based review
- [JAK INHIBITORS FOR THE TREATMENT OF ALOPECIA AREATA].
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- COVID-19 and Autoimmunity in Dermatology: A Moroccan Case Series and Literature Review
- Update From 2017 Embracing the World of Dermatology Convention
- The molecular basis of human keratin disorders
- Trichohyalin-Like Proteins Have Evolutionarily Conserved Roles in the Morphogenesis of Skin Appendages
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Bachmann–Bupp syndrome and treatment
- Molecular Genetics of Human Hair Diseases
- Platelet-Rich Plasma Therapy for Male and Female Pattern Hair Loss