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Research 511–540 of 1000+
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Male Pattern Baldness
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Dermoscopic findings in female androgenetic alopecia
- The Effect of Plasma Rich in Growth Factors on Pattern Hair Loss: A Pilot Study
- Family History and Risk of Hair Loss
- Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Efficacy and Safety of Long-Pulsed 755-nm Alexandrite Laser for Keratosis Pilaris: A Split-Body Randomized Clinical Trial
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- Health Utility of Facial Angiofibroma associated with Tuberous Sclerosis Complex
- From Hairline to Lipid Line: Prevalence and Spectrum of Dyslipidemia in Patients with Androgenetic Alopecia – A Hospital-Based Study
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- HAIR REGROWTH
- Review paper The use of reflectance confocal microscopy in selected inflammatory skin diseases
- Acquired progressive kinking of hair affecting the scalp and eyelashes in an adult woman
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Hair Loss: A Harbinger of the Morbidities to Come!
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- A Review on Ayurvedic Niadanatmak Concept of Khalityavyadhi
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Ischemic onycholysis of the hands
- Bhangra: Therapeutic and Pharmacological Actions in Shayb (Premature Greying of Hair)
- Androgenic Alopecia and Homoeopathic Management