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Research 631–660 of 1000+
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- An Excellent Response to Tofacitinib in a Pediatric Alopecia Patient: A Case Report and Review.
- Hyperpigmentation following Treatment of Frontal Fibrosing Alopecia
- [JAK INHIBITORS FOR THE TREATMENT OF ALOPECIA AREATA].
- Platelet-Rich Plasma (PRP) in Dermatology: Cellular and Molecular Mechanisms of Action
- Confluent and Reticulated Papillomatosis Associated with Polycystic Ovarian Syndrome
- Classification of psychodermatological disorders: Proposal of a new international classification
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Cyclin-Dependent Kinase 4/6 Inhibitors and Dermatologic Adverse Events: Results from the EADV Task Force “Dermatology for Cancer Patients” International Study
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- First Symposium of Ichthyosis Experts
- Effectiveness and Safety Profile of Oral Tofacitinib in Alopecia Areata: An Observational Study from a Tertiary Hospital
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Aqueous Dispersion of Unmodified Fullerene C60: Stimulation of Hair Growth and Study of a New Molecular Target for Interaction
- Avian-Inspired Analogies in Dermatology
- 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
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Culprits of Medication-Induced Telogen Effluvium, Part 1
- Diagnosis and Management of Alopecia Areata: A Saudi Expert Consensus Statement (2023)
- Review on Alopecia Areata in the Middle East and Africa: Landscape and Unmet Needs
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Alopecia Areata in Latin America: Where are We and Where are We Going?
- Hair shaft disorders: a rare case series
- Ginseng in Hair Growth and Viability
- Update From 2017 Embracing the World of Dermatology Convention