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    Sort by

    Research 511–540 of 1000+

    1. A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica Nasza Dermatologia Online · 2013 · 5 citations
    2. Patterns of noncicatricial alopecia in children: a cross-sectional study Al-Azhar Assiut Medical Journal · 2023
    3. AAPS and PSRC 2016 Abstract Supplement Plastic and reconstructive surgery. Global open · 2016
    4. Subject Index Journal of the American Academy of Dermatology · 2008
    5. Clinical Applications of Punch-Based Techniques in Dermatologic Surgery Clinical Cosmetic and Investigational Dermatology · 2026
    6. Quality of life in children and adolescents with alopecia areata—A systematic review Journal of the European Academy of Dermatology and Venereology · 2023 · 39 citations
    7. Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities 2016 · 36 citations
    8. Inherited epidermolysis bullosa: clinical and therapeutic aspects Anais Brasileiros de Dermatologia · 2013 · 32 citations
    9. Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart Journal of Investigative Dermatology · 2004 · 22 citations
    10. A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report BMC dermatology · 2018 · 18 citations
    11. Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population Molecular genetics and metabolism reports · 2019 · 8 citations
    12. Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis Dermatology and Therapy · 2024 · 3 citations
    13. British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology British Journal of Dermatology · 2010 · 136 citations
    14. Pleiotropic Role of Notch Signaling in Human Skin Diseases International Journal of Molecular Sciences · 2020 · 29 citations
    15. Total Facelift: Forehead Lift, Midface Lift, and Neck Lift Archives of Plastic Surgery · 2015 · 20 citations
    16. Androgen Treatment in Adolescent Males With Hypogonadism American journal of men's health · 2020 · 19 citations
    17. Subcellular localization of the five members of the human steroid 5α-reductase family Biochimie open · 2017 · 13 citations
    18. Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82 Nature communications · 2022 · 9 citations
    19. Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings Indian Journal of Dermatology Venereology and Leprology · 2012 · 9 citations
    20. Complex X chromosome rearrangement associated with multiorgan autoimmunity Molecular cytogenetics · 2015 · 8 citations
    21. Incidence, complications and therapeutic evaluation of clinical hypothyroidism in different breeds of dogs BMC Veterinary Research · 2025 · 1 citations
    22. Real-world safety of ixekizumab: a disproportionality analysis using the FDA adverse event reporting system and the VigiAccess databases Frontiers in Medicine · 2025
    23. Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report. Case Reports in Dermatology · 2025
    24. Multiple Concurrent Pilonidal Sinuses: Case report and Literature review Judi Clinical Journal · 2025
    25. Androgenetic Alopecia: A Review Nigerian Postgraduate Medical Journal · 2024
    26. Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles Journal of Investigative Dermatology · 2006 · 38 citations
    27. Erosive pustular dermatosis of the scalp: challenges and solutions Clinical, Cosmetic and Investigational Dermatology · 2019 · 13 citations
    28. Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework Diagnostics · 2026
    29. The molecular basis of human keratin disorders Human Genetics · 2009 · 79 citations
    30. Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families Human Genetics · 2010 · 40 citations