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Research 541–570 of 1000+
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Biology of the Hair Follicle: The Basics
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Emerging concepts about prenatal genesis, aberrant metabolism and treatment paradigms in polycystic ovary syndrome
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Yellow dots in trichoscopy: relevance, clinical significance and peculiarities
- Heterogeneity of Polymorphous Light Eruption: A Study of 105 Patients
- Definition criteria and diagnostic assessments
- Side Effects of 5‐Alpha Reductase Inhibitors: A Comprehensive Review
- Poster Abstracts
- SUMMARIES OF PAPERS
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Fibroblast bioelectric signaling drives hair growth
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Baricitinib in the Management of Coexisting Alopecia Areata and Atopic Dermatitis: A Case Report
- Monilethrix: A rare hereditary condition
- Hair Anomalies in a 6-Year-Old Girl
- Telogen Effluvium
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Ashwagandha root in the treatment of non-classical adrenal hyperplasia
- PA33 When bones speak through nails: insights from a paediatric case series
- Scarring Alopecia in Pediatric Patients: A Narrative Review of Etiologies, Diagnosis, and Management Strategies
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Practical approaches to the use of markers of biochemical hyperandrogenism in women
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Monilethrix