Search
for
Sort by
Research 451–480 of 1000+
- The lack of significant changes in scalp hair follicle density with advancing age
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Evaluation of SALT score severity in correlation with trichoscopic findings in alopecia areata: a study of 303 patients
- Traditional and Integrative Approaches to the Treatment of Alopecia
- Frontotemporal dementia with parkinsonism presenting as posterior cortical atrophy
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- Mapping of cis-acting expression quantitative trait loci in human scalp hair follicles
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- The Clinical Presentation of Systemic Lupus Erythematosus
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE
- British Society for Dermatopathology
- Evaluating the Effect of the Demographic, Trichoscopic and Laboratory Characteristics on The Recurrence of Alopecia Areata
- Afamin serum concentrations are associated with insulin resistance and metabolic syndrome in polycystic ovary syndrome
- Risk Factors for Male Lower Urinary Tract Symptoms: The Role of Metabolic Syndrome and Androgenetic Alopecia in a Latin American Population
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Causal associations between plasma proteins and prostate cancer: a Proteome-Wide Mendelian Randomization
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Polycystic ovary syndrome
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Cutaneous manifestations associated with COVID-19 infection at a university hospital in eastern China
- Repurposing FDA approved drugs for psoriasis indications through integrated molecular docking, one-SVM algorithm, and molecular dynamics simulation approaches
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Serum Cystatin C levels in adolescent females: A comparative study between PCOS and Non-PCOS groups
- Efficacy of modern methods for assessing the severity of alopecia areata