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Research 91–120 of 1000+
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Animals in Dermatology
- Acne Syndromes and Mosaicism
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- The Genetics of Human Skin Disease
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Genetic Hair Disorders: A Review
- Hormonal Effects on Hair Follicles
- Idiopathic unilateral facial hirsutism
- Current Genetics in Hair Diseases
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Physiological perspective of Hirsutism in Unani Medicine: An Overview and Update
- Hirsutism
- Madarosis
- The Role of Histone Demethylases in Disease
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Nails and hair
- Skin Development and Disease: A Molecular Perspective
- Hair Loss in Children, Etiologies, and Treatment
- Eyelash Trichomegaly: A Rare Presenting Feature of Systemic Lupus Erythematosus.
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Pregnancy and Skin
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Management of Facial Hair in Women
- Endocrine evaluation of hirsutism