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Research 391–420 of 1000+
- The pathogenesis of alopecia areata
- Drug-Induced Hair Loss and Hair Growth
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- Efectos adversos dermatológicos con uso de litio
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- Obsessive-compulsive disorder in dermatology
- Alopecia Areata: Current Review
- Dermal papilla cells and melanocytes response to physiological oxygen levels depends on their interactions
- British Association of Dermatologists living guideline for managing people with alopecia areata 2024
- Dramatic and persistent loss of eyelashes
- Nutritional Dermatoses in the Hospitalized Patient
- British Association of Dermatologists living guideline for managing people with alopecia areata 2025
- Culprits of Medication-Induced Telogen Effluvium, Part 1
- Case Report: Dermoscopic features of oral lichen planus - the evolution of mucoscopy
- [Loss of hair due to vitamin A].
- The Spectrum of Cutaneous Manifestations in Lupus Erythematosus: A Comprehensive Review
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- RASopathic Skin Eruptions during Vemurafenib Therapy
- Utility of dermoscopy in alopecia areata
- The RAIG Family Member, GPRC5D, Is Associated with Hard-Keratinized Structures
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Pregnancy and Skin
- A medicinal and edible formula YH0618 ameliorates the toxicity induced by Doxorubicin via regulating the expression of Bax/Bcl-2 and FOXO4
- Cronkhite-Canada Syndrome (CCS)—A Rare Case Report
- Hyperpigmented Upper Eyelid: A Clue to the Diagnosis of Facial Lichen Planus Pigmentosus in a Patient with Frontal Fibrosing Alopecia
- Trichoscopic patterns of nonscarring alopecia's
- Cases Report the Cronkhite-Canada Syndrome
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita