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    Research 181–210 of 1000+

    1. In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis Pharmaceuticals · 2023
    2. Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit) Journal of complementary medicine & alternative healthcare · 2023
    3. Causes and Management of Hypertrichosis American Journal of Clinical Dermatology · 2002 · 61 citations
    4. Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations Frontiers in Pharmacology · 2026
    5. Hair Disorders Springer eBooks · 2018
    6. Minoxidil-induced hypertrichosis: Pathophysiology, clinical implications, and therapeutic strategies JAAD reviews. · 2024 · 7 citations
    7. <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review International Research Journal of Ayurveda & Yoga · 2026
    8. Síndrome do nevo de Becker Anais Brasileiros De Dermatologia · 2010 · 21 citations
    9. Minoxidil induced hypertrichosis in a 2 year-old child F1000Research · 2013 · 17 citations
    10. Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III Cardiology in Review · 2002 · 15 citations
    11. Cutaneous Granular Cell Tumor with Overlying Hypertrichosis in an Adult: A Rare Case Report Dermatopathology · 2026
    12. Trichoscopy of aplasia cutis congenita of the scalp in skin of color Journal of Cosmetic Dermatology · 2023
    13. Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2 2022 · 8 citations
    14. Two females with hair loss Journal der Deutschen Dermatologischen Gesellschaft · 2019
    15. Reversal of male-pattern baldness, hypertrichosis, and accelerated hair and nail growth in patients receiving benoxaprofen. BMJ · 1982 · 34 citations
    16. Acne in Dark Skin Springer eBooks · 2018 · 5 citations
    17. Pili Torti: A Feature of Numerous Congenital and Acquired Conditions Journal of clinical medicine · 2021 · 9 citations
    18. Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families Human Genetics · 2010 · 40 citations
    19. Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia The American Journal of Human Genetics · 2012 · 74 citations
    20. Low-dose oral minoxidil in a case of short anagen syndrome Journal of Dermatological Treatment · 2025
    21. Diagnosis and Management of Hair Loss in Pediatric Berkala Ilmu Kesehatan Kulit dan Kelamin · 2024
    22. A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies 2022 · 2 citations
    23. Answer International Journal of Pediatrics and Adolescent Medicine · 2015 · 1 citations
    24. Hair: more than just an appendage International journal of research in dermatology · 2021
    25. Genetic hair and nail disorders Clinics in dermatology · 2005 · 37 citations
    26. Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene Journal of Molecular Neuroscience · 2022 · 9 citations
    27. Cholesterol homeostasis in hair follicle keratinocytes is disrupted by impaired ABCA5 activity Biochimica and biophysica acta. Molecular and cell biology of lipids · 2023
    28. Acquired trichomegaly with topiramate Journal of the American Academy of Dermatology · 2005 · 24 citations
    29. [Hirsutism]. PubMed · 1993
    30. More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players Journal of Investigative Dermatology · 2006 · 35 citations