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Research 841–870 of 1000+
- Tangled Causes, Targeted Solutions: A Comprehensive Review of Alopecia.
- Differences in Demographic and Clinical Characteristics Among Subtypes of Female Pattern Hair Loss
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Acne keloidalis nuchae: prevalence, impact, and management challenges
- Acquired scalp alopecia. Part I: A review
- SKIN AND HAIR COSMETIC ISSUES IN WOMEN OF COLOR
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Near-complete regrowth in Alopecia totalis following individualized homeopathic management at Dr. Batra’s®: A case report
- Analysis of Skin, Hair and Nail Diseases in the Adults with Beta Thalassemia Major
- PREFACE
- Westwood Carolina Conference on Clinical Dermatology
- Support for dermatological research in Sub‐Saharan Africa: insights from African hair and skin research programs
- Trichotillomania Across Circuits: Neurobiology, Sensory Processing, and Genetic Insights
- Intrinsic and Extrinsic Factors Associated with Hair Graying (Canities) and Therapeutic Potential of Plant Extracts and Phytochemicals
- Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris
- Association of epidemiological and biochemical factors with premature graying of hair: A case–control study
- Intrinsic factors in the pathogenesis of hidradenitis suppurativa: Genetics, hormones, and the microbiome
- The natural history of androgenetic alopecia
- When hair dig into the brain, JAKi , may help!
- A case study of homeopathic treatment for alopecia areata at Dr. Batra’s clinic
- Serum levels of vitamin C, vitamin E, and total antioxidant capacity in premature graying hair
- Vaccines, Infections, and Alopecia Areata
- Central Centrifugal Cicatricial Alopecia: New Insights and a Call for Action
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- In vivo reflectance confocal microscopy: usefulness for diagnosing hair diseases
- An induced pluripotent stem cell-based approach for hair follicle development and regeneration
- Learning from nudity: lessons from the nude phenotype
- Common Skin Disorders in Pediatric Skin of Color
- Female pattern hair loss—An update