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    Research 661–690 of 1000+

    1. Dimensionality and psychometric analysis of DLQI in a Brazilian population Health and Quality of Life Outcomes · 2020 · 22 citations
    2. CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation American journal of ophthalmology. Case reports · 2017 · 9 citations
    3. Cutaneous extramedullary haematopoiesis: Implications in human disease and treatment Experimental Dermatology · 2019 · 6 citations
    4. Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma Frontiers in Oncology · 2024
    5. Análise comparativa entre os tratamentos para alopecia: uma revisão sistemática Research, Society and Development · 2021
    6. Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient Journal of Clinical Medicine · 2025
    7. Ichthyosis with confetti: clinics, molecular genetics and management Orphanet Journal of Rare Diseases · 2015 · 36 citations
    8. Scaffold-based developmental tissue engineering strategies for ectodermal organ regeneration Materials Today Bio · 2021 · 22 citations
    9. Enriching Proteolysis Targeting Chimeras with a Second Modality: When Two Are Better Than One Journal of Medicinal Chemistry · 2022 · 10 citations
    10. Management of folliculitis decalvans: The EADV task force on hair diseases position statement Journal of the European Academy of Dermatology and Venereology · 2025 · 5 citations
    11. Hair India 2010 International Journal of Trichology · 2010 · 2 citations
    12. Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies? Function · 2022
    13. How rare is isolated rheumatic tricuspid valve disease? Journal of Mind and Medical Sciences · 2020
    14. Inherited epidermolysis bullosa: clinical and therapeutic aspects Anais Brasileiros de Dermatologia · 2013 · 32 citations
    15. De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia BMC Medical Genomics · 2024 · 3 citations
    16. Synchronous pancreas and gallbladder cancer with concomitant alopecia totalis Turkish Journal of Surgery · 2023 · 1 citations
    17. Pathophysiology of Androgenetic Alopecia and Implications for Treatment: An Overview of Current Literature Journal of Biosciences and Medicines · 2026
    18. p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis Journal of Investigative Dermatology · 2015 · 19 citations
    19. The mineralocorticoid receptor as a novel player in skin biology: beyond the renal horizon? Experimental Dermatology · 2009 · 40 citations
    20. Persistent hair growth during treatment with the EGFR inhibitor erlotinib Dermatology Online Journal · 2009 · 39 citations
    21. New developments in the molecular treatment of ichthyosis: review of the literature Orphanet journal of rare diseases · 2022 · 21 citations
    22. Therapeutic effect of mesenchymal stem cells on histopathological, immunohistochemical, and molecular analysis in second-grade burn model Stem Cell Research & Therapy · 2021 · 10 citations
    23. Primary idiopathic pseudopelade of brocq: Five case reports International Journal of Trichology · 2014 · 7 citations
    24. Cancer-Related Alopecia: From Etiologies to Global Management Cancers · 2021 · 4 citations
    25. Hair diseases: a big problem on a small surface Postepy Dermatologii I Alergologii · 2016 · 4 citations
    26. Post-marketing safety signals of four JAK inhibitors for alopecia areata: an indication-restricted FAERS pharmacovigilance study Journal of Dermatological Treatment · 2026 · 2 citations
    27. Hair follicle stem cells promote epidermal regeneration under expanded condition Frontiers in physiology · 2024
    28. Effect of injectable calcium alginate-amelogenin hydrogel on macrophage polarization and promotion of jaw bone osteogenesis 2023
    29. Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report Frontiers in Medicine · 2025
    30. Male infertility and genitourinary birth defects: there is more than meets the eye Fertility and Sterility · 2020 · 26 citations