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Research 901–930 of 1000+
- Parents May Over-report Use of Home Safety Interventions
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- BH07: Testosterone deficiency in men with female pattern hair loss
- Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management
- JAK inhibitors for alopecia areata: a systematic review and meta‐analysis
- Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency revisited: an update with a special focus on adolescent and adult women
- Drug repurposing: A novel strategy to target cancer stem cells and therapeutic resistance
- Tofacitinib therapy for children with severe alopecia areata
- Neuropsychiatric Systemic Lupus Erythematosus Presenting as Bipolar I Disorder With Catatonic Features
- Overview of Ultrasound Imaging Applications in Dermatology
- Preclinical Challenges in Proton Minibeam Radiotherapy: Physics and Biomedical Aspects
- Current Treatments for Alopecia Areata
- Prevalence of alopecia areata in Japan: Estimates from a nationally representative sample
- Treatment of moderate-to-severe alopecia areata in pre-adolescent children with baricitinib
- Preparation and Characterization of Solution-Processed Nanocrystalline p-Type CuAlO2 Thin-Film Transistors
- A.S.P.E.N. Parenteral Nutrition Trace Element Product Shortage Considerations
- Disorders of hair in infants and children other than alopecia
- Advancements in transdermal drug delivery using microneedles: technological and material perspective
- Hair loss among a group of Egyptian children
- Androgenic alopecia: an entity to consider in adolescence
- Special Focus Issue: Transdermal, Topical and Folicular Drug Delivery Systems
- TNF-α Inhibitor-Induced Psoriasis and Psoriatic Alopecia in Adolescent with Ulcerative Colitis: Clinical Case
- Switching JAK inhibitors: evaluating baricitinib’s effectiveness in alopecia areata after tofacitinib failure
- Traction alopecia: Neglected in women and children of color
- Serially expanded flap use to treat large hairless scalp lesions
- Lasers for Hair Removal
- Advances in genetic and molecular understanding of Omenn syndrome - implications for the future
- A Case of Acrodermatitis Enteropathica