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Research 541–570 of 1000+
- CENTRAL STATES DERMATOLOGICAL SOCIETY
- PREFACE
- Risk of Polycystic Ovary Syndrome in Women Exposed to Fine Air Pollutants and Acidic Gases: A Nationwide Cohort Analysis
- Erythrokeratodermia Variabilis
- Occipital donor area grading and profile in Indian population
- Alopecia Areata
- Research Snippets
- A Canadian Algorithm on the Management of Telogen Effluvium.
- TGF-β family signaling in stem cells
- Edible seeds from Cucurbitaceae family as potential functional foods: Immense promises, few concerns
- Implanon<sup>®</sup> and alopecia
- The History of Hair Transplantation
- COVID-19-induced hair shedding and related risk factors: A Saudi perspective
- The stag as an historical source of materia medica
- Historical Archives
- A History of Drug Advertising: The Evolving Roles of Consumers and Consumer Protection
- Parenting Styles and Psychological Effects on Children with Alopecia Areata: Exploring Family Dynamics, Anxiety, and Depression
- Structures of three polycystic kidney disease-like domains from<i>Clostridium histolyticum</i>collagenases ColG and ColH
- Alopecia in preexisting autoimmune thyroid disease in family medicine practice: can hyperprolactinemia induce hair loss? A case report
- Historical and Current Adenosine Receptor Agonists in Preclinical and Clinical Development
- The natural history of androgenetic alopecia
- A family business: stem cell progeny join the niche to regulate homeostasis
- Analytical chemistry studying historical pharmaceuticals and health care formulations
- Canities subita: sudden blanching of the hair in history and literature
- Darier Sign: A Historical Note
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome