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    Research 211–240 of 1000+

    1. Trichothiodystrophy with Dysmyelination and Central Osteosclerosis American Journal of Neuroradiology · 2010 · 16 citations
    2. New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report BMC Medical Genetics · 2017 · 23 citations
    3. Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images Clinical Case Reports · 2025
    4. 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증 대한피부과학회지 · 2011
    5. Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness 2021
    6. Genetically modified laboratory mice with sebaceous glands abnormalities Cellular and Molecular Life Sciences · 2016 · 22 citations
    7. Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix Journal of Investigative Dermatology · 1999 · 20 citations
    8. Alopezien und Hypotrichosen im Kindesalter Der Hautarzt · 2014 · 5 citations
    9. ¿Qué esconde la alopecia? Alopecia universalis como síntoma de inicio de un paciente seropositivo al VIH Galicia Clínica · 2022
    10. Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin Development · 2012 · 82 citations
    11. Autoimmune Disease Induction in a Healthy Human Organ: A Humanized Mouse Model of Alopecia Areata Journal of Investigative Dermatology · 2012 · 75 citations
    12. Immunology of alopecia areata 2020 · 23 citations
    13. Pathophysiology of Alopecia Areata in the Pediatric Patient Pediatric Dermatology · 2025 · 5 citations
    14. A Clinical Review of Trichorrhexis Nodosa The Open Dermatology Journal · 2025
    15. Trichoscopy in alopecias: Diagnosis simplified International Journal of Trichology · 2013 · 96 citations
    16. Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome Anais Brasileiros de Dermatologia · 2015 · 30 citations
    17. A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies 2022 · 2 citations
    18. Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells Nature communications · 2014 · 99 citations
    19. The role of the skin microbiome in the development of alopecia areata Journal of Education, Health and Sport · 2022
    20. Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles Journal of Investigative Dermatology · 2016 · 50 citations
    21. Multi-omics and AI-driven advances in miRNA-mediated hair follicle regulation in cashmere goats Frontiers in Veterinary Science · 2025 · 2 citations
    22. Revisiting the role of melatonin in human melanocyte physiology: A skin context perspective Journal of pineal research · 2022 · 26 citations
    23. Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review Clinical endocrinology · 2008 · 26 citations
    24. Taiwanese Dermatological Association consensus on the diagnosis and management of alopecia areata Dermatologica Sinica · 2025 · 4 citations
    25. Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential Experimental Dermatology · 2019 · 21 citations
    26. Skin Development and Disease: A Molecular Perspective Current Issues in Molecular Biology · 2024 · 15 citations
    27. Melanocytes: The new Black The International Journal of Biochemistry & Cell Biology · 2006 · 93 citations
    28. Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant Genes · 2025
    29. Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis Frontiers in Medicine · 2025
    30. Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair Dermatologic Therapy · 2016 · 3 citations