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Research 421–450 of 1000+
- Congenital Trichomegaly of the Eyelashes
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Training requirements and recommendation for the specialty of dermatology and venereology <i>European Standards of Postgraduate Medical Specialist Training</i>
- Evaluation and Treatment of Hirsutism in Premenopausal Women: An Endocrine Society Clinical Practice Guideline
- Drug Repurposing for Rare Diseases
- Involvement of mechanical stress in androgenetic alopecia
- Advancing Regenerative Cellular Therapies in Non-Scarring Alopecia
- Premature hair graying: a multifaceted phenomenon
- Adipose-derived stem cells applied in skin diseases, wound healing and skin defects: a review
- A comprehensive review of platelet-rich plasma for the treatment of dermatologic disorders
- Cutaneous manifestations of endocrine diseases in children
- Male androgenetic alopecia
- Hair Loss, Diagnosis, and Treatment Planning
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Hair regeneration using microneedle-assisted human basic fibroblast growth factor
- Current understanding and treatment of sex hormone-related hair diseases
- Association of Acne Tarda with Endocrinological Disorders
- Compliance to Topical Minoxidil and Reasons for Discontinuation among Patients with Androgenetic Alopecia
- Factors associated with female pattern hair loss and its prevalence in Taiwanese women: A community-based survey
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Identification of lncRNAs involved in the hair follicle cycle transition of cashmere goats in response to photoperiod change
- Androgenetic Alopecia: a Review and Emerging Treatments
- Androgenetic alopecia
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- Topical minoxidil therapy in hereditary androgenetic alopecia
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor