Search
for

    Sort by

    Research 181–210 of 1000+

    1. Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation Frontiers in pediatrics · 2022
    2. Editor’s picks January 2021 Journal of the European Academy of Dermatology and Venereology · 2021
    3. Alopecia Areata KARGER eBooks · 2008 · 24 citations
    4. Birt–Hogg–Dubé syndrome Familial cancer · 2013 · 7 citations
    5. Fish Cell Spheroids, a Promising In Vitro Model to Mimic In Vivo Research: A Review Cells · 2024 · 5 citations
    6. Evaluating the Causal Relationship Between Human Blood Metabolites and the Susceptibility to Alopecia Areata Journal of Cosmetic Dermatology · 2025 · 1 citations
    7. Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies Current Protocols · 2024
    8. A Prospective Study of the Prevalence of Nonclassical Congenital Adrenal Hyperplasia among Women Presenting with Hyperandrogenic Symptoms and Signs The Journal of Clinical Endocrinology and Metabolism · 2007 · 150 citations
    9. Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K. British Journal of Dermatology · 2012 · 1 citations
    10. Combined hormonal contraception and venous thromboembolism The European Journal of Contraception & Reproductive Health Care · 2007 · 46 citations
    11. Current aspects of polycystic ovary syndrome: A literature review Revista Da Associacao Medica Brasileira · 2016 · 15 citations
    12. A patient with combined polycystic ovary syndrome and autoimmune polyglandular syndrome type 2 Gynecological Endocrinology · 2007 · 9 citations
    13. Early-onset baldness and the risk of aggressive prostate cancer: findings from a case–control study Cancer Causes & Control · 2017 · 4 citations
    14. Workup and Management of Polycystic Ovary Syndrome Springer eBooks · 2015
    15. Anthracycline analogs The past, present, and future Cancer Chemotherapy and Pharmacology · 1986 · 168 citations
    16. Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient Molecular genetics & genomic medicine · 2021 · 3 citations
    17. Advances in precise cell manipulation Droplet · 2025 · 9 citations
    18. A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene Clinical Case Reports · 2025
    19. Ehlers-Danlos syndrome: From bedside to bench Frontiers research topics · 2024
    20. Molecular and physiological mechanisms underlying the antifungal and nutrient acquisition activities of beneficial microbes 2016 · 3 citations
    21. Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant Pediatrics International · 2026
    22. Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome ˜The œAmerican journal of case reports · 2018 · 14 citations
    23. When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman The Neurologist · 2022 · 3 citations
    24. Role of Drug Repurposing in Sustainable Drug Discovery IntechOpen eBooks · 2023
    25. Polycystic ovary syndrome Practical diabetes · 2005 · 8 citations
    26. Primary High‐Grade Ovarian Sertoli–Leydig Cell Tumor With Bilateral Adnexal Involvement in a Patient Diagnosed With Peutz–Jeghers Syndrome Case Reports in Oncological Medicine · 2025
    27. 2022 Update on Prostate Cancer Epidemiology and Risk Factors—A Systematic Review European Urology · 2023 · 710 citations
    28. Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome JAMA Dermatology · 2015 · 33 citations
    29. Bioengineered Skin Intended as In Vitro Model for Pharmacosmetics, Skin Disease Study and Environmental Skin Impact Analysis Biomedicines · 2020 · 26 citations
    30. Murine Cytomegalovirus is Not Associated With Alopecia Areata in C3H/HeJ Mice Journal of Investigative Dermatology · 1998 · 25 citations