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    Research 331–360 of 1000+

    1. Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report Clinical Cosmetic and Investigational Dermatology · 2023
    2. Ectodermal Dysplasia: Variable Expressions Indian Journal of Dermatology · 2025
    3. Special collection on inward rectifying K<sup>+</sup> channels American journal of physiology. Cell physiology · 2023 · 3 citations
    4. Stem Cells Applications in Regenerative Medicine and Disease Therapeutics International Journal of Cell Biology · 2016 · 606 citations
    5. Top applications of dermatologic ultrasonography that can modify management ULTRASONOGRAPHY · 2022 · 36 citations
    6. Minoxidil induced hypertrichosis in a 2 year-old child F1000Research · 2013 · 17 citations
    7. Eyebrow and Eyelash Alopecia: A Clinical Review American journal of clinical dermatology · 2022 · 6 citations
    8. Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin Maturation The Journal of Cell Biology · 1998 · 79 citations
    9. Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia Children · 2023 · 4 citations
    10. Harnessing Regenerative Science in Aesthetic Surgery: The Biologically Driven Future Journal of Clinical Medicine · 2025 · 2 citations
    11. Exploring the knowledge, attitudes, and perceptions of young men towards fertility in the UK: A cross-sectional survey PLoS ONE · 2026
    12. Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders Annals of Dermatology · 2026
    13. Unraveling Translational Insights into Systemic Multi-Organ Toxicity of Cytosine Arabinoside (Ara-C): A Systematic Review of Preclinical Animal Evidence Current Issues in Molecular Biology · 2025
    14. 861 Frontal fibrosing alopecia (FFA) under dynamic optical coherence tomography (D-OCT) Journal of Investigative Dermatology · 2017 · 1 citations
    15. A Clinical Approach to Severe Insulin Resistance KARGER eBooks · 2007 · 32 citations
    16. Multi-dermatomal unilateral nevus comedonicus along the lines of Blaschko: a rare presentation International journal of research in dermatology · 2017
    17. Male fertility and skin diseases Reviews in Endocrine and Metabolic Disorders · 2016 · 12 citations
    18. Hormone therapy for transgender patients Translational Andrology and Urology · 2016 · 146 citations
    19. The Skin and Subcutaneous Tissues Springer eBooks · 2013 · 1 citations
    20. An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery Clinical Cosmetic and Investigational Dermatology · 2025
    21. Book Reviews International Journal of Cosmetic Surgery and Aesthetic Dermatology · 2002
    22. Novel missense mutation in the EDA gene in a family affected by oligodontia 2016 · 12 citations
    23. Síndrome PRIDE: una práctica forma de identificar los efectos adversos cutáneos de los inhibidores del EGFR Revista Medicina Cutánea Ibero-Latino-Americana · 2021
    24. Polycystic ovary syndrome (PCOS) Annales D Endocrinologie · 2010 · 40 citations
    25. PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS) Anticancer Research · 2018 · 21 citations
    26. Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency Endocrine journal · 2019 · 13 citations
    27. A Critical Review on Obstetric Follow-up of Women Affected by Systemic Lupus Erythematosus Revista Brasileira de Ginecologia e Obstetrícia · 2018 · 12 citations
    28. A comprehensive guide to upper lip aesthetic rejuvenation Journal of cosmetic dermatology · 2019 · 9 citations
    29. Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment 2018 · 1 citations
    30. Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia Orphanet Journal of Rare Diseases · 2026