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    Research 541–570 of 1000+

    1. Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment 2018 · 1 citations
    2. Neonatal Occipito-Lınear and Temporo-Fronto-Parıetal Alopecıa: Can Non-Marginal and Marginal forms of the Transient Neonatal Hair Loss be Found Together? Hair therapy & transplantation · 2014 · 1 citations
    3. Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome The Journal of Dermatology · 2014 · 1 citations
    4. Female Hairline Preference among Various Segments of the Korean Population Annals of Dermatology · 2014 · 1 citations
    5. The Skin and Subcutaneous Tissues Springer eBooks · 2013 · 1 citations
    6. Woolly Antics between the Sheaths Journal of Investigative Dermatology · 2009 · 1 citations
    7. Volumes 2 and 3: The Head and Neck (Parts 1 and 2) Plastic and Reconstructive Surgery · 2007 · 1 citations
    8. Book Reviews Journal of Paediatrics and Child Health · 1999 · 1 citations
    9. TREATMENT OF KERATOSIS PILARIS: A NARRATIVE LITERATURE REVIEW OF TOPICAL, PROCEDURAL, AND VARIANT-SPECIFIC THERAPIES International Journal of Innovative Technologies in Social Science · 2026
    10. Alopecia and Its homoeopathic treatment International Journal of Homoeopathic Sciences · 2026
    11. Minoxidil e óleo essencial de alecrim: proposta de solução tópica para alopecia androgenética Revista Ensaios Pioneiros · 2026
    12. <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review International Research Journal of Ayurveda & Yoga · 2026
    13. Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot Human Genome Variation · 2026
    14. CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy Cureus · 2026
    15. Exploring the therapeutic potential of naturally occurring taxifolin, a dietary flavonoid: an updated comprehensive review Frontiers in Pharmacology · 2026
    16. 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
    17. Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations Frontiers in Pharmacology · 2026
    18. Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts Forum Dermatologicum · 2026
    19. Techniques d'épargne cutanée dans la chirurgie de la gynécomastie Archive ouverte UNIGE (University of Geneva) · 2026
    20. Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation Journal of Clinical and Investigative Dermatology · 2026
    21. The Association Between 5α-Reductase Inhibitors and the Presence of Subsequent Dry Eye Disease in Androgenetic Alopecia: A TriNetX Database Study Cureus · 2025
    22. Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis Frontiers in Medicine · 2025
    23. 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
    24. Predicting Polycystic Ovary Syndrome among Reproductive-Aged Women in Bangladesh Using Machine Learning Algorithms: Development of a Hospital-Based Predictive Model 2025
    25. A rare case of chronic genian fistula with oral mucosal hair follicle inclusion: case report and review of the literature Frontiers in Oral Health · 2025
    26. Farmácia São Lázaro - Porto e nos Serviços Farmacêuticos do Hospital Privado de Vila Real (Grupo Trofa Saúde) - Vila Real Open Repository of the University of Porto (University of Porto) · 2025
    27. Fourth Nerve Palsy After Hair Replacement Surgery and Prolonged Vertical Position in a Patient With Mega-Cisterna-Magna: Report of a Case Cureus · 2025
    28. Farmácia Aliança - Maia Open Repository of the University of Porto (University of Porto) · 2025
    29. Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications Cureus · 2025
    30. Expanding the Senior-Løken syndrome spectrum: Combined Rothmund-Thomson features unveil the distinct Teelwani Syndrome phenotype 2025