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Research 571–600 of 1000+
- Disease Versus Disease: How One Disease May Ameliorate Another
- Exploring the effects of Chinese herbal ingredients on the signaling pathway of alopecia and the screening of effective Chinese herbal compounds
- Identification of Potential Hub Genes in Alopecia Areata
- Identification and characterization of genes for skin and hair disorders
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- sc-eQTL unveil Immunogenetic Architecture of Polycystic Ovary Syndrome
- A second case of effective eradication of alopecia areata following treatment with the dopaminergic drug dextroamphetamine
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Psoriasis of the scalp – the current state of the problem
- Clinical Snippets
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Androgenetic alopecia: An autosomal dominant disorder
- Regulatory T cells in skin mediate immune privilege of the hair follicle stem cell niche
- Periodontal Ligament Stem Cells: Regenerative Potency in Periodontium
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Persistent Hypoglycemia and Macrosomia in a Newborn
- An Unusual “Side Effect” of an Acne Drug
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- [Effectiveness of the treatment plan for androgenetic alopecia].
- Heterozygous 21‐hydroxylasedeficiency as a cause of hyperandrogenism
- Warfarin: almost 60 years old and still causing problems
- Diagnostic approach to low‐renin hypertension
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- Engineering Cell Surfaces with Polyelectrolyte Materials for Translational Applications
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Botulinum toxin type A for the management of hidradenitis suppurativa.
- LAMELLAR ICHTHYOSIS: ONE CASE REPORT
- Alopecia Areata
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Hair follicle stem cells and the collapse of self-tolerance in alopecia: the interplay of barrier function, the microbiome, and immunity