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    Research 151–180 of 1000+

    1. 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
    2. A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents Frontiers in Medicine · 2017 · 40 citations
    3. Clinical relevance of hair microscopy in alopecia Clinical and Experimental Dermatology · 2002 · 15 citations
    4. Congenital atrichia associated with situs inversus and mesocardia International journal of trichology · 2012 · 5 citations
    5. Marie-unna hereditary hypotrichosis International Journal of Trichology · 2014 · 4 citations
    6. A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family 2018 · 9 citations
    7. Congenital atrichia associated with nevus flammeus: A rare association Indian dermatology online journal · 2014 · 2 citations
    8. An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis Journal of Investigative Dermatology · 2006 · 97 citations
    9. 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
    10. Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex American journal of human genetics · 2018 · 55 citations
    11. Hairless is a nuclear receptor corepressor essential for skin function Nuclear Receptor Signaling · 2009 · 30 citations
    12. 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
    13. Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient Journal of dermatology · 2013 · 2 citations
    14. ĮGIMTA NERANDĖJANTI SKALPO ALOPECIJA: KLINIKINIS ATVEJIS IR DIFERENCINĖ DIAGNOSTIKA Health Sciences · 2025
    15. Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report Frontiers in Medicine · 2025
    16. Hypotrichosis in a child with olmsted syndrome Indian Dermatology Online Journal · 2018
    17. Editors' Picks Journal of Investigative Dermatology · 2010
    18. Biology and Genetics of Hair Annual Review of Genomics and Human Genetics · 2010 · 89 citations
    19. Causes and Management of Hypertrichosis American Journal of Clinical Dermatology · 2002 · 61 citations
    20. HAIR AND SYSTEMATIC DISEASE Dermatologic Clinics · 2001 · 58 citations
    21. Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations Frontiers in Pharmacology · 2026
    22. Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit) Journal of complementary medicine & alternative healthcare · 2023
    23. Hair Disorders Springer eBooks · 2018
    24. To grow or not to grow: Hair morphogenesis and human genetic hair disorders Seminars in Cell & Developmental Biology · 2013 · 43 citations
    25. Minoxidil-induced hypertrichosis: Pathophysiology, clinical implications, and therapeutic strategies JAAD reviews. · 2024 · 7 citations
    26. <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review International Research Journal of Ayurveda & Yoga · 2026
    27. Síndrome do nevo de Becker Anais Brasileiros De Dermatologia · 2010 · 21 citations
    28. Minoxidil induced hypertrichosis in a 2 year-old child F1000Research · 2013 · 17 citations
    29. Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle British Journal of Dermatology · 2014 · 25 citations
    30. Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III Cardiology in Review · 2002 · 15 citations