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    Research 961–990 of 1000+

    1. Safety concerns of paternal drug exposure on fertility, pregnancy and offspring: An analysis based on the FDA adverse event reporting system Andrology · 2024
    2. What Work-Up Should Be Done for Patients With Alopecia? CRC Press eBooks · 2024
    3. 301 The Spectrum of PLEC Sequence Variants and Related Plectinopathies Including Novel Association with Epidermolysis Bullosa Pruriginosa Journal of Investigative Dermatology · 2022
    4. Early Onset Werner Syndrome Turkish Journal of Endocrinology and Metabolism · 2015
    5. Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I International Journal of Trichology · 2013
    6. Abstracts Congenital Anomalies · 2016 · 1 citations
    7. Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review Pediatric Dermatology · 2025
    8. Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance? Wiener medizinische Wochenschrift · 2020 · 7 citations
    9. Eflúvio telógeno após dermatite de contato no couro cabeludo Anais Brasileiros de Dermatologia · 2006 · 4 citations
    10. Trichonodosis: a case report and literature review Skin Appendage Disorders · 2025
    11. A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix 2011 · 3 citations
    12. Gene detection in a family with monilethrix and treatment with 5% topical minoxidil Skin research and technology · 2022 · 2 citations
    13. Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis Frontiers in Medicine · 2025
    14. Brief study of hypertrichosis International Journal For Multidisciplinary Research · 2025
    15. Hair Shaft Abnormalities – Clues to Diagnosis and Treatment Dermatology · 2005 · 44 citations
    16. Lichen Planopilaris-Like Changes Arising within an Epidermal Nevus: Does This Case Suggest Clues to the Etiology of Lichen Planopilaris? Journal of cutaneous medicine and surgery · 2000 · 12 citations
    17. Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation European Journal of Dermatology · 2010 · 11 citations
    18. Canestick Lesion of Vellus Hair in Netherton's Syndrome Archives of Dermatology · 1985 · 9 citations
    19. Cutaneous Manifestations of Endocrine Disease Harper's Textbook of Pediatric Dermatology · 2019 · 4 citations
    20. A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix 生物医学研究杂志:英文版 · 2011 · 3 citations
    21. Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome The Journal of Dermatology · 2014 · 1 citations
    22. Bilateral Xen is Used as Minimally Invasive Glaucoma Surgery for Glaucoma in GAPO Syndrome: Case Report Journal of College of Physicians And Surgeons Pakistan · 2025
    23. Tricorrexis nodosa localizada Revista del Centro Dermatológico Pascua · 2024
    24. An unusual case of quadruple polyorchidism in a human cadaver mimicking bilateral lipoma European journal of anatomy · 2022
    25. Delayed Puberty Springer eBooks · 2016
    26. P142 – 3046: Encephalocraniocutaneous lipomatosis, a rare neurocutaneous disorder: Report of additional three cases European Journal of Paediatric Neurology · 2015
    27. Pesticides Exposure and Risk of Hypospadias InTech eBooks · 2011
    28. Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia 2009 · 42 citations
    29. Unruly hair British Journal of Dermatology · 1985 · 19 citations
    30. Short anagen syndrome: Case series and literature review Pediatric Dermatology · 2018 · 13 citations