Search
for
Sort by
Research 241–270 of 870
- Alopecia Areata: An Update on Treatment Options for Children
- Tinea Capitis in Elderly Women: A Report of 4 Cases
- Hair follicles modulate skin barrier function
- Editorial: Mesenchymal Stromal Cell Therapy for Regenerative Medicine
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- ALKBH5-mediated m6A demethylation fuels cutaneous wound re-epithelialization by enhancing PELI2 mRNA stability
- Dietary Vitamin A Impacts Refractory Telogen
- Managing Skin Ageing as a Modifiable Disorder—The Clinical Application of Nourella® Dual Approach Comprising a Nano-Encapsulated Retinoid, Retilex-A® and a Skin Proteoglycan Replacement Therapy, Vercilex®
- The Immunological Association between Alopecia Areata and Respiratory Diseases: A Systematic Review
- Inhibition of TNF-α-Induced Collagen Degradation and Oxidative Damage by Centipeda minima and Brevilin A in Human Dermal Fibroblasts
- Exploring the Role of Dermal Sheath Cells in Wound Healing and Fibrosis
- Alopecia Areata
- Scalp Involvement in Primary Cutaneous Lymphomas—An Update on Clinical Presentation, Diagnostics, and Management
- Juvenile versus maturity-onset alopecia areata- a comparative retrospective clinical study
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Characterization of<i>CDH3</i>-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Extensive Ichthyosiform Sarcoidosis in a Patient With Juvenile Rheumatoid Arthritis
- Hypotrichosis with juvenile macular dystrophy
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- Lipidized Fibrous Histiocytoma: Differential Diagnosis from Juvenile Xanthogranuloma
- 81 Juvenile RHUPUS syndrome: a case reports
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- P050 Rapidly worsening subcutaneous oedema in a young boy: a case of juvenile dermatomyositis
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Low Free Thyroxine (FT4) in critically ill juvenile systemic lupus erythematosus: a diagnostic approach
- Juvenile systemic lupus erythematosus presenting only as nonscarring alopecia
- Juvenile diabetes mellitus with exocrine pancreatic insufficiency in a Thai Bangkaew dog: a case report