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Research 181–210 of 1000+
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Androgenetic, Diffuse and Senescent Alopecia in Men: Practical Evaluation and Management
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Treatment of Hair Loss
- Frontal Fibrosing Alopecia: An Update on Pathogenesis, Diagnosis, and Treatment
- Male pattern baldness: current treatments, future prospects
- Androgenic alopecia: A counterproductive outcome of the anabolic effect of androgens
- Common Baldness in Women
- Types and Treatment of Hair Loss in Men and Women
- Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations
- Androgenetic Alopecia: Therapy Update
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Congenital hair loss disorders: Rare, but not too rare
- Short anagen syndrome
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Secondary cicatricial and other permanent alopecias
- Male fertility and skin diseases
- Dermatopathology and molecular genetics
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- Alopecia and Its homoeopathic treatment
- Erythromelanosis Follicularis Faciei et Colli: A Case Report
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Oral Presentations