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    Research 121–150 of 1000+

    1. Analysis of hair loss in young adults- A clinical study International journal of dermatology, venereology and leprosy sciences · 2019
    2. Trichoscopy in hair disorders in darker skin: An approach to diagnosis Clinical dermatology review · 2020 · 3 citations
    3. Hair diseases: a big problem on a small surface Postepy Dermatologii I Alergologii · 2016 · 4 citations
    4. Genetic Hair Disorders: A Review Dermatology and Therapy · 2019 · 26 citations
    5. A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers The American Journal of Human Genetics · 1998 · 83 citations
    6. Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia The American Journal of Human Genetics · 2012 · 74 citations
    7. A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle Genes · 2021 · 2 citations
    8. Mesenchymal Stem Cells With Modification of Junctional Adhesion Molecule A Induce Hair Formation Stem cells translational medicine · 2014 · 8 citations
    9. Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis Proceedings of the National Academy of Sciences of the United States of America · 2013 · 44 citations
    10. Alopecia in Epidermolysis Bullosa Dermatologic Clinics · 2009 · 21 citations
    11. Genetically modified laboratory mice with sebaceous glands abnormalities Cellular and Molecular Life Sciences · 2016 · 22 citations
    12. Hair loss and its management in children Expert Review of Dermatology · 2011 · 5 citations
    13. Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis Frontiers in Medicine · 2025
    14. Hair loss Postgraduate Medicine · 1986 · 9 citations
    15. Diseases of Periocular Hair Survey of Ophthalmology · 2011 · 7 citations
    16. Aging of hair Journal of Cosmetic Dermatology · 2005 · 99 citations
    17. Hair and scalp disorders Medicine · 2004 · 2 citations
    18. Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family Dermatology Reports · 2011 · 1 citations
    19. Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype PLOS genetics · 2019 · 24 citations
    20. Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report Clinical Case Reports · 2026
    21. Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases Indian Dermatology Online Journal · 2025
    22. Claves diagnósticas en displasias pilosas II 2021 · 2 citations
    23. Trichoscopic Findings in Androgenetic Alopecia Medicinski arhiv · 2021 · 3 citations
    24. Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases International Journal of Molecular Sciences · 2020 · 57 citations
    25. Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome American journal of human genetics · 2020 · 34 citations
    26. Dermatological problems of the puberty Postepy Dermatologii I Alergologii · 2013 · 18 citations
    27. Commonly associated disorders with complete scalp alopecia in early childhood: A review International journal of trichology · 2023
    28. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex American journal of human genetics · 2018 · 55 citations
    29. Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity Clinical Cosmetic and Investigational Dermatology · 2025
    30. Hair fragility (trichorrhexis nodosa) in alopecic Pomeranian dogs Veterinary Dermatology · 2024 · 1 citations