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Research 961–990 of 1000+
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Clinical Presentations and Comorbidities of Pediatric Alopecia Areata
- Acne Tarda and Male-Pattern Baldness Unmasking Primary Ovarian Insufficiency: A Case and Review
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Diagnosis and management of hair loss in children
- Skin Organoids for Disease Modelling, Drug Screening and Regenerative Medicine: Recent Advances and Future Perspectives
- Long‐term culture of skin biopsies: maintenance of fibroblast production and competency of reprogramming
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Skin-Derived Stem Cells for Wound Treatment Using Cultured Epidermal Autografts: Clinical Applications and Challenges
- The Parathyroid Hormone Second Receptor PTH2R and its Ligand Tuberoinfundibular Peptide of 39 Residues TIP39 Regulate Intracellular Calcium and Influence Keratinocyte Differentiation
- Collagen Involvement in Health, Disease, and Medicine
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Epidemiology, diagnosis, and management of polycystic ovary syndrome
- Polycystic Ovary Syndrome
- Trichotillomania
- Proteome Analysis of Human Hair Shaft
- Vitamin D and the Skin: An Update for Dermatologists
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- 6 Current concepts of polycystic ovary syndrome
- Associaton of Insulin Resistance Linked Diseases and Hair Loss in Elderly Men. Finnish Population-based Study
- Lysophospholipid Mediators in Health and Disease
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Pleiotropic Role of Notch Signaling in Human Skin Diseases
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Hair Shaft Dysplasias
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases
- Androgens and hair: a biological paradox