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Research 661–690 of 1000+
- Alopecia areata incognita: A Hypothesis
- Dermoscopic evaluation of therapeutic response to an intralesional corticosteroid in the treatment of alopecia areata
- Topical minoxidil in the treatment of alopecia areata.
- Quality of life in South African Black women with alopecia: a pilot study
- Effect of betulin oil on hair growth in hypothyroidism- a long-term blinded pilot study
- Optimizing skin disease diagnosis: harnessing online community data with contrastive learning and clustering techniques
- Minoxidil-induced hypertrichosis in a child with alopecia areata
- A Decade With Sheehan's Syndrome: A Case Report and Personal Experience.
- Pediatric and Adolescent Alopecia Areata Treated with JAK Inhibitors: Balancing Efficacy and Safety Across Clinical Trials
- Trichotillomania associated with a 25-hydroxy vitamin D deficiency: A case report
- Trichoscopic Features of Syphilitic Alopecia and Alopecia Areata: A Comparative Study
- Effectiveness and safety of baricitinib in severe alopecia areata: 48-week results
- Dermatologist and Patient Perceptions of Treatment Success in Alopecia Areata and Evaluation of Clinical Outcome Assessments in Japan
- Sensitisation to ethylhexyl salicylate: Another piece of the frontal fibrosing alopecia puzzle
- An Overview of Commonly Used Natural Alternatives for the Treatment of Androgenetic Alopecia, with Special Emphasis on Rosemary Oil
- Transcriptome analysis of frontal fibrosis alopecia revealed involvement of immune cells and ferroptosis
- Trichotillomania
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Acquired trichomegaly with topiramate
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Teneligliptin-induced hair loss: A case report
- Common causes of paediatric alopecia
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening
- Concomitant Alopecia Areata and Profound Bone Marrow Suppression: An Unusual Manifestation of Azathioprine Toxicity
- Widespread and eruptive comedonal lesions with alopecia
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- A phase 2a randomized, placebo-controlled study to evaluate the efficacy and safety of the oral Janus kinase inhibitors ritlecitinib and brepocitinib in alopecia areata: 24-week results