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Research 241–270 of 1000+
- Alopecia Areata
- Mesenchymal Stromal Cell Secretome: Influencing Therapeutic Potential by Cellular Pre-conditioning
- Alopecia areata
- Tofacitinib for the treatment of severe alopecia areata and variants: A study of 90 patients
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Weakly supervised learning of biomedical information extraction from curated data
- SFRP2/DPP4 and FMO1/LSP1 Define Major Fibroblast Populations in Human Skin
- Safety and efficacy of the JAK inhibitor tofacitinib citrate in patients with alopecia areata
- Dermatoses of pregnancy
- Regulatory T-Cells: Potential Regulator of Tissue Repair and Regeneration
- Demodicosis and rosacea: Epidemiology and significance in daily dermatologic practice
- Decreased Serum Ferritin is Associated With Alopecia in Women
- Probing the Effects of Stress Mediators on the Human Hair Follicle
- An Update of Congenital Adrenal Hyperplasia
- Cachexia and graft-vs.-host-disease-type skin changes in keratin promoter-driven TNF alpha transgenic mice.
- Clinical manifestations of cutaneous lupus erythematosus
- Epidemiology and burden of alopecia areata: a systematic review
- Lupus erythematosus: systemic and cutaneous manifestations
- Dermatological adverse events with taxane chemotherapy
- Exosomes for repair, regeneration and rejuvenation
- Cutaneous manifestations of systemic lupus erythematosus
- Extraskeletal actions of vitamin D
- Drug-Induced Skin, Nail and Hair Disorders
- Sex differences in SARS-CoV-2 infection rates and the potential link to prostate cancer
- Interferon in the treatment of cutaneous T-cell lymphoma
- Treatment of Obstructive Sleep Apnea Improves Cardiometabolic Function in Young Obese Women with Polycystic Ovary Syndrome
- Cutaneous reactions to recombinant cytokine therapy
- Hair Follicle Immune Privilege Revisited: The Key to Alopecia Areata Management
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency