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    Research 511–540 of 1000+

    1. Interventions for central serous chorioretinopathy: a network meta-analysis Cochrane library · 2015 · 87 citations
    2. Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles Journal of Investigative Dermatology · 2016 · 50 citations
    3. Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments Journal of Investigative Dermatology · 2024 · 32 citations
    4. Therapeutic effect of mesenchymal stem cells on histopathological, immunohistochemical, and molecular analysis in second-grade burn model Stem Cell Research & Therapy · 2021 · 10 citations
    5. The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China Clinical Cosmetic and Investigational Dermatology · 2021 · 10 citations
    6. Metabolic Syndrome, Hepatic Steatosis and Testosterone: A Matter of Sex Livers · 2024 · 7 citations
    7. Forensic approach in cases of anabolic-androgenic steroid abuse and cardiovascular mortality: insights from autopsy, histopathology, immunohistochemistry and toxicology Frontiers in Cardiovascular Medicine · 2025 · 1 citations
    8. Polycystic ovary syndrome in Singapore Annals Academy of Medicine Singapore · 2022 · 1 citations
    9. Pharmacovigilance profiles of three generations of mineralocorticoid receptor antagonists and network toxicology analysis Frontiers in Medicine · 2026
    10. Hair follicle stem cells promote epidermal regeneration under expanded condition Frontiers in physiology · 2024
    11. A Case of Ovarian Hyperthecosis in a Postmenopausal Woman JCEM Case Reports · 2023
    12. PCOS in Adolescents—Ongoing Riddles in Diagnosis and Treatment Journal of Clinical Medicine · 2023 · 5 citations
    13. Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome American journal of human genetics · 2020 · 34 citations
    14. Diagnosis and Management of Polycystic Ovary Syndrome in Adolescent Girls Pediatric Annals · 2015 · 20 citations
    15. Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families Molecular genetics & genomic medicine · 2022 · 5 citations
    16. The 46th Annual Meeting of the Irish Endocrine Society Meeting Programme and Abstracts 2022 Irish Journal of Medical Science (1971 -) · 2024
    17. The effect of gonadoliberin analog treatment in precocious puberty on polycystic ovarian syndrome prevalence in adulthood Frontiers in endocrinology · 2024
    18. Association of Acne Tarda with Endocrinological Disorders Dermato · 2022
    19. [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II 2022
    20. Toxic and Metabolic Disorders of the Nervous System CRC Press eBooks · 2007
    21. Polycystic Ovary Syndrome: Etiology, Current Management, and Future Therapeutics Journal of Clinical Medicine · 2023 · 380 citations
    22. Polycystic ovary syndrome (PCOS) and COVID-19: an overlooked female patient population at potentially higher risk during the COVID-19 pandemic BMC Medicine · 2020 · 112 citations
    23. Polycystic Ovary Syndrome: An Updated Overview Foregrounding Impacts of Ethnicities and Geographic Variations Life · 2022 · 49 citations
    24. Inflammatory perspectives of polycystic ovary syndrome: role of specific mediators and markers Middle East Fertility Society Journal · 2023 · 31 citations
    25. Structure of human steroid 5α-reductase 2 with the anti-androgen drug finasteride Nature Communications · 2020 · 30 citations
    26. New developments in the molecular treatment of ichthyosis: review of the literature Orphanet journal of rare diseases · 2022 · 21 citations
    27. Polycystic Ovary Syndrome and Reproductive Health: A Comprehensive Review Clinical and Experimental Obstetrics & Gynecology · 2024 · 9 citations
    28. 11-Oxyandrogens in Adolescents With Polycystic Ovary Syndrome Journal of the Endocrine Society · 2022 · 9 citations
    29. Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA) Orphanet Journal of Rare Diseases · 2022 · 8 citations
    30. Exploring Pediatric Dermatology in Skin of Color: Focus on Dermoscopy Life · 2024 · 4 citations