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Research 61–90 of 1000+
- Updates on Hirsutism: A Narrative Review
- Drug-Induced Skin, Nail and Hair Disorders
- Dermatologic manifestations of endocrine disorders
- Diagnosis of hyperandrogenism: clinical criteria
- Hair Disorders
- Clinical Perspectives on Alopecia: From Hair Follicle Biology to Advanced Therapies
- Hair Loss in Children
- Focal and Generalized Alopecia
- Skin manifestations of endocrine diseases
- Hair and scalp disorders
- Managing the PCOS-Related Symptoms of Hirsutism, Acne, and Hair Loss
- Reversal of Baldness in Patient Receiving Minoxidil for Hypertension
- Evidence-based approach to cutaneous hyperandrogenism in women
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Anagen effluvium
- Hair Disorders
- Calcineurin-based immunosuppression in renal transplantation : focus on efficacy, the role of steroids, and the cardiovascular risk
- Molecular Genetics of Alopecias
- Hair Shafts in Trichoscopy
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Congenital hair loss disorders: Rare, but not too rare
- Canine alopecia X-Like disorder
- Paraneoplastic alopecia associated with internal malignancies in the cat
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study
- Androgenetic Alopecia: Therapy Update
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report