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Research 781–810 of 1000+
- Diagnostic approach to low‐renin hypertension
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Identifying causal genes in alopecia areata using integrative analysis of differential expression and Mendelian randomization
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Nonclassic adrenal hyperplasia
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- The Clinical Presentation of Systemic Lupus Erythematosus
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Quantitative analysis and development of alopecia areata classification frameworks
- THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE
- Bioaesthetics and regenerative medicine
- British Society for Dermatopathology
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Role of skin enzymes in metabolism of topical drugs
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Integrative Whole-Transcriptome Sequencing Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Ethnicity, obesity and the prevalence of impaired glucose tolerance and type 2 diabetes in PCOS: a systematic review and meta-regression
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- The G1/S transition in mammalian stem cells in vivo is autonomously regulated by cell size
- Woolly Antics between the Sheaths
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Platelet-Rich Plasma in the Management of Alopecia: A Systematic Review and Meta-Analysis of Clinical Evidence
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Immunoglobulin E and Serum Interleukin-13 and Bacteria in Patients with Alopecia Areata
- Clinical and anamnestic features of alopecia areata in ukrainian men