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Research 331–360 of 1000+
- Ocular Cosmetics in Modern Times
- Selected topics in pediatric hair loss
- Contents
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Cutaneous manifestations of systemic lupus erythematosus
- Dissecting folliculitis (dissecting cellulitis) of the scalp: a 66‐patient case series and proposal of classification
- Drug eruptions in dermatology
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Fourth Nerve Palsy After Hair Replacement Surgery and Prolonged Vertical Position in a Patient With Mega-Cisterna-Magna: Report of a Case
- Telogen Effluvium
- CUTANEOUS MANIFESTATIONS OF LUPUS ERYTHEMATOSUS FROM A TERTIARY CARE CENTRE IN COASTAL KERALA
- An Update of Congenital Adrenal Hyperplasia
- A study on dermatoses of pregnancy
- Trichoscopic evaluation of frontal hairline recession in Egyptian female patients
- Scalp Bogginess in the Presence of Lichen Planopilaris: Isolated Occurrence or Reactionary Process?
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair
- Physiology and Medical Treatments for Alopecia
- Clinico-epidemiological study of alopecia areata
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Aseptic Necrosis of Warts Instead of Lymphangitis
- Demodicosis and rosacea: Epidemiology and significance in daily dermatologic practice
- Congenital adrenal hyperplasia
- Safety of Janus Kinase inhibitors in Patients with Alopecia Areata: A Systematic Review
- A Bibliometric Analysis of Alopecia Areata Literature over the Past 50 Years.
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- A clinico-epidemiological study of non-scarring alopecia in a tertiary care centre
- Hair loss after covid 19 - case series