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Research 61–90 of 1000+
- Alopecia Areata Update
- Diagnostic challenges in determining alopecia areata
- Molecular Genetics of Alopecias
- Alopecia and its medical management
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Alopecia and Thyroid Disease
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Congenital hair loss disorders: Rare, but not too rare
- Alopecia Areata
- Management of congenital ichthyoses: European guidelines of care, part two
- Alopecia areata: An update
- Alopecia Areata
- Alopecia Areata
- Approach to the adult female patient with diffuse nonscarring alopecia
- Acquired scalp alopecia. Part I: A review
- Alopecia and Its homoeopathic treatment
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Androgenetic Alopecia
- Acquired scalp alopecia. Part II: A review
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Marie-unna hereditary hypotrichosis
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Abstracts Pt.30
- Non-Neoplastic Disorders of Hair
- Updates in the understanding and treatments of skin & hair disorders in women of color
- Morphological Approach to Hair Disorders
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Thyroid hormone action on skin.
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs