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Research 61–90 of 1000+
- Central hair loss in African American women: Incidence and potential risk factors
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- New developments in the molecular treatment of ichthyosis: review of the literature
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- A Bidirectional Mendelian Randomization Study of Androgenetic Alopecia and Obesity
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Exploring links with rare variants, COVID-19 and short anagen hair syndrome
- Male-pattern baldness susceptibility locus at 20p11
- The biology of hair diversity
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Role of insulin resistance and diet in acne
- Evaluation of serum level of omentin‐1 in females with hirsutism
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Etiopathogenesis of Alopecia Areata
- The role of family history and its influence on the onset time in female pattern hair loss
- Alopecia and the Aging Male
- Reply to ‘What is the effect of obesity on the folliculosebaceous unit?’
- Main Plenary Sessions: Summaries of Papers
- Prevalence and Etiology of Central Centrifugal Cicatricial Alopecia
- Análise dos níveis de metilação e de polimorfismos genéticos dos genes GSTP1, MGMT, VDR e AR em pacientes com câncer de próstata
- Impact of Premature Greying of Hair on Socio-cultural Adjustment and Self-esteem among Medical Undergraduates in Foundation University, Islamabad
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- The Rotterdam Study: 2016 objectives and design update
- Frontal Fibrosing Alopecia
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- The Glucocorticoid Resistance Syndrome. Two Cases of a Novel Pathogenic Variant in the Glucocorticoid Receptor Gene
- Mult-trait analysis of GWAS - Perceived youtfulness - UKBB
- The role of WNT10B in physiology and disease: A 10-year update