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    Research 841–870 of 1000+

    1. Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report Frontiers in Genetics · 2025
    2. 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH Journal of the Endocrine Society · 2024
    3. Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient Frontiers in medicine · 2024
    4. Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1 Pediatric Dermatology · 2024
    5. Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review Biomedicines · 2024
    6. This month in JAAD Case Reports: October 2023—Central centrifugal cicatricial alopecia in Black men Journal of the American Academy of Dermatology · 2023
    7. T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy 2022
    8. Clouston’s syndrome: a rare case report International Journal of Research in Dermatology · 2020
    9. SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS Journal of the Endocrine Society · 2020
    10. Utilizing functional genomics approaches to characterize risk genes in alopecia areata Columbia Academic Commons (Columbia University) · 2020
    11. An Infant with Worsening Rash ˜The œjournal of applied laboratory medicine · 2018
    12. Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities Neuropediatrics · 2012
    13. News in brief Expert Review of Dermatology · 2011
    14. First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy Clinical Biochemistry · 2007
    15. Hairless: A nuclear receptor corepressor essential for skin function Advances in developmental biology · 2006
    16. This Month in the Journal The American Journal of Human Genetics · 2005
    17. Genetic analysis of the role of androgen metabolism in the pathogenesis of prostate cancer SUNScholar (Stellenbosch University) · 2004
    18. Hutchinson-gilford progeria syndrome and its relevance to cardiovascular diseases and normal aging. PubMed · 2013 · 3 citations
    19. A Case of Steatocystoma Multiplex in a Psoriatic Patient during Treatment with Anti-IL-12/23 Skin Appendage Disorders · 2020 · 2 citations
    20. Hutchinson-Gilford progeria syndrome - A brief introduction International Journal of Pharmacological Research · 2018 · 2 citations
    21. Acrodermatitis enteropathica – a diagnostic challenge: case report of late-onset, genetically proven disease with normal zinc serum levels Pediatria i Medycyna Rodzinna · 2025 · 1 citations
    22. A case of 21-hydroxylase deficiency in Turner′s syndrome and literature review Zhonghua neifenmi daixie zazhi · 2017 · 1 citations
    23. A Newborn With Hair Loss Clinical pediatrics · 2013 · 1 citations
    24. HDL as Therapeutic Tools Springer eBooks · 2019
    25. Severe Hypernatremia as Presentation of Netherton Syndrome Global Medical Genetics · 2023
    26. Acrodermatitis enteropathica – diagnostic challenges Research Square (Research Square) · 2023
    27. Hair follicle associated pluripotent (HAP) stem cells jump from transplanted whiskers to pelage follicles and stimulate hair growth Scientific Reports · 2022
    28. An unusual presentation of vitamin D dependent rickets type 2 with low 25 (OH) D3 levels and alopecia: a case report of two siblings International Journal of Contemporary Pediatrics · 2022
    29. Deletion of an enhancer in FGF5 is associated with ectopic expression in goat hair follicles and the cashmere growth phenotype Research Square (Research Square) · 2020
    30. ATRICHIA WITH PAPULAR LESIONS – A CASE REPORT Journal of evolution of medical and dental sciences · 2012