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    Research 421–450 of 1000+

    1. Management of High-energy Avulsive Ballistic Facial Injury: A Review of the Literature and Algorithmic Approach Plastic and Reconstructive Surgery – Global Open · 2018 · 16 citations
    2. Atlas of Geriatric Dermatology Springer eBooks · 2014 · 2 citations
    3. HAIR | Overview Elsevier eBooks · 2000 · 2 citations
    4. Lipid nanocarriers as innovative strategies for hair regrowth Discover Nano · 2026
    5. Complications in Esthetic Surgery InTech eBooks · 2016
    6. BH09 Mycophenolate mofetil in the management of lichen planus pigmentosus in a woman with frontal fibrosing alopecia British Journal of Dermatology · 2024 · 1 citations
    7. Widespread and eruptive comedonal lesions with alopecia JAAD case reports · 2022
    8. Coexistence of dermatomyositis and alopecia areata: Insight into pathogenesis Indian Dermatology Online Journal · 2018
    9. Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases Indian Dermatology Online Journal · 2025
    10. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex American journal of human genetics · 2018 · 55 citations
    11. Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions Journal of Investigative Dermatology · 2006 · 81 citations
    12. Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless Journal of Investigative Dermatology · 2000 · 29 citations
    13. Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless Journal of Investigative Dermatology · 2000 · 4 citations
    14. Hair restoration surgery: pre-surgical considerations and pitfalls Plastic and Aesthetic Research · 2024
    15. A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report Journal of Comprehensive Pediatrics · 2022
    16. Monilethrix, a rare inherited hair shaft disorder in siblings Indian dermatology online journal · 2014 · 4 citations
    17. Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening Journal of the American Academy of Dermatology · 2012 · 3 citations
    18. Gene detection in a family with monilethrix and treatment with 5% topical minoxidil Skin research and technology · 2022 · 2 citations
    19. Trichothiodystrophy without associated neuroectodermal features in two siblings International Journal of Trichology · 2018 · 2 citations
    20. Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review Pediatric Dermatology · 2025
    21. Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree Frontiers in Genetics · 2025
    22. Real-world Burden of Disease and Clinical Characteristics of Alopecia Areata Among Adults in Brazil: Results from a Cross-sectional Survey Dermatology and Therapy · 2026
    23. Coexistent frontal fibrosing alopecia with ophiasis pattern alopecia areata in a young female: A case report and review of the literature Clinical Case Reports · 2024
    24. Are Sunscreen Particles Involved in Frontal Fibrosing Alopecia?—A TEM-EDXS Analysis on Formalin-Fixed Paraffin-Embedded Alopecia Biopsies (Pilot Study) 2022
    25. Genetic Hair Disorders: A Review Dermatology and Therapy · 2019 · 26 citations
    26. Ectodermal Dysplasia: Variable Expressions Indian Journal of Dermatology · 2025
    27. Trichoscopy in Unveiling the Triad of Netherton Syndrome Clinical Dermatology Review · 2025
    28. Alopecia universalis following human papillomavirus vaccine administration: a case report Clinical and Experimental Vaccine Research · 2025
    29. Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family Journal of clinical laboratory analysis · 2021 · 4 citations
    30. A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome Orphanet Journal of Rare Diseases · 2017 · 11 citations