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Research 391–420 of 690
- Hair loss and its management in children
- Advances in Hair Diseases
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- Marie-unna hereditary hypotrichosis
- Safety of Janus Kinase inhibitors in Patients with Alopecia Areata: A Systematic Review
- A study on the association between thyroid dysfunction and various dermatoses in northeastern India
- A Case of Rhupus with Rowell Syndrome
- Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- Assessing the burden of dermatological diseases on work life from a gender perspective
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Exuberant tufted folliculitis
- Hair Follicle Reconstruction and Stem Cells
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- Inherited Disorders of the Hair
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- LUPUS ERYTHEMATOSUS AND THE SKIN
- Optimizing skin disease diagnosis: harnessing online community data with contrastive learning and clustering techniques
- Efectos adversos dermatológicos con uso de litio
- Evaluation of COVID-19 risk in patients on systemic retinoid therapy
- British Hair and Nail Society
- Trichodystrophies: A hair-raising differential diagnosis
- Plaque psoriasis
- Primary cicatricial alopecias
- Upadacitinib in dermatologic therapy: Emerging evidence and expanding indications
- Spectrum and clinical burden of Unrecognized Dermatologic Diseases in hospitalized adults: A single-centre cross-sectional study
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot