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Research 901–930 of 1000+
- Investigation of exacerbating factors for postpartum hair loss: a questionnaire-based cross-sectional study
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Faun tail nevus: A series of 15 cases and their management with Intense Pulse Light
- Hair casts
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Study of the Thyroid Profile of Patients with Alopecia
- Hair-Based Assessment of Sex Steroid Hormones in Patients with Anorexia Nervosa
- Microneedling combined with compound betamethasone in treatment of severe alopecia areata: A case report
- Global Impact of Coronavirus Disease 2019 (COVID-19)
- Serenoa repens induced erectile dysfunction: Underdiagnosis and phytovigilance
- Parameters of obesity in polycystic ovary syndrome
- Magistral Galenic Preparations in Modern Dermatology: Our Top 10 Picks for Bridging Therapeutic Gaps
- Alopecia Areata in Sub-Saharan Africa: A Scoping Review Protocol on Epidemiology, Clinical Presentation, Burden, Treatment, and Evidence Gaps.
- Ophthalmologic Comorbidities in Alopecia Areata
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- 20 years of the socioeconomic impact of atopic dermatitis and alopecia areata from around the globe
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- 7745 Hirsutism in young girls: Beyond PCOS
- Rare Association of Congenital Triangular Alopecia with Vitiligo
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- The feasibility and utility of hair follicle sampling to measure FMRP and FMR1 mRNA in children with or without fragile X syndrome: a pilot study
- Nothing about us, without us: Are we asking the right questions in transgender research?
- Immune-mediated Coombs negative intravascular haemolysis in systemic lupus erythematosus (SLE)
- Introductory Chapter: Polycystic Ovarian Disease: The Rainbow Without Color (SPECTRUM)
- Human hair growth in vitro: a model for the study of hair follicle biology