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    Research 61–90 of 1000+

    1. Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity Clinical Cosmetic and Investigational Dermatology · 2025
    2. Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population Skin Health and Disease · 2025
    3. Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families Molecular genetics & genomic medicine · 2022 · 5 citations
    4. Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia 2009 · 42 citations
    5. Hair: more than just an appendage International journal of research in dermatology · 2021
    6. Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix Experimental Dermatology · 2015 · 18 citations
    7. Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review Pediatric Dermatology · 2025
    8. Hair That Is Difficult to Manage in a Hispanic Girl Skin appendage disorders · 2017 · 1 citations
    9. Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation American Journal of Medical Genetics - Part A · 2010 · 11 citations
    10. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family British Journal of Dermatology · 2000 · 36 citations
    11. Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II Pediatric Dermatology · 2016 · 14 citations
    12. Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report European Journal of Dermatology · 2018
    13. Management of congenital ichthyoses: European guidelines of care, part two British Journal of Dermatology · 2018 · 66 citations
    14. The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report Egyptian Journal of Medical Human Genetics · 2024
    15. Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family Acta Scientific Paediatrics · 2023
    16. <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case Вопросы современной педиатрии · 2023
    17. Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I Pediatric Dermatology · 2016 · 33 citations
    18. Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost Journal of The European Academy of Dermatology and Venereology · 2004 · 22 citations
    19. Editors' Picks Journal of Investigative Dermatology · 2010
    20. Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses Archives of Dermatology · 2001 · 23 citations
    21. Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation Journal of Clinical and Investigative Dermatology · 2026
    22. Hair Loss in Children Elsevier eBooks · 2018
    23. A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice 2008 · 60 citations
    24. Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics International Journal of Dermatology Venereology and Leprosy Sciences · 2024
    25. Secondary cicatricial and other permanent alopecias Dermatologic Therapy · 2008 · 20 citations
    26. A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents Frontiers in Medicine · 2017 · 40 citations
    27. Hair Loss in Children Current problems in dermatology · 2015 · 24 citations
    28. Clinical relevance of hair microscopy in alopecia Clinical and Experimental Dermatology · 2002 · 15 citations
    29. To grow or not to grow: Hair morphogenesis and human genetic hair disorders Seminars in Cell & Developmental Biology · 2013 · 43 citations
    30. Hairless is a nuclear receptor corepressor essential for skin function Nuclear Receptor Signaling · 2009 · 30 citations