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Research 181–210 of 1000+
- 396 Vδ1 + T-cells are stress-sentinels in human skin and are implicated in alopecia areata pathogenesis
- An Unusual Case of Diarrhea, Dysgeusia, and Grainy and Nodular Mucosa
- PRESEPTAL CELLULITIS DUE TO IMPETIGO – A CASE REPORT OF UNCOMMON PRESENTATION IN PAKISTAN
- Philological Obfuscation
- Psoriatic Alopecia
- Hair Mesotherapy
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- The ProScope HR: A promising diagnostic tool
- “Nail loss after teriflunomide treatment: A new potential adverse event”
- S127 Regulation of hair growth
- Alopecia Induced by Fluoroscopy-guided Embolization: A Case Report
- S123 The pathological dynamics of androgenetic alopecia and its treatment
- Le retentissement psychologique des pathologies chroniques du cheveu
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Prevention of chemotherapy drug-mediated human hair follicle damage: combined use of cooling with antioxidant suppresses oxidative stress and prevents matrix keratinocyte cytotoxicity
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Index
- Beneficial effect of spironolactone on androgenic alopecia
- Clinical case of alopecia totalis in pediatric practice
- Lifestyle Drugs in Old Age – A Mini-Review
- Oral Presentations
- Cutaneous Drug Reaction Case Reports
- Post-menopausal frontal fibrosing alopecia
- Alopecia Areata and Habit Tic Deformities
- SHAREABLE RESOURCE
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Clinical Case Notes. Tamoxifen optic neuropathy
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children