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    Research 601–630 of 1000+

    1. Evaluation of lipid levels in androgenetic alopecia in comparison with control group Journal of The European Academy of Dermatology and Venereology · 2008 · 27 citations
    2. Flutamide in the treatment of hirsutism International journal of gynaecology and obstetrics · 1991 · 27 citations
    3. A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene British Journal of Dermatology · 2011 · 26 citations
    4. Combined Oral Contraception and Bicalutamide in Polycystic Ovary Syndrome and Severe Hirsutism: A Double-Blind Randomized Controlled Trial The Journal of Clinical Endocrinology & Metabolism · 2017 · 25 citations
    5. Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets Arquivos Brasileiros de Endocrinologia & Metabologia · 2008 · 24 citations
    6. Influence of <i>FHIT</i> on benzo[ <i>a</i> ]pyrene-induced tumors and alopecia in mice: Chemoprevention by budesonide and <i>N</i> -acetylcysteine Proceedings of the National Academy of Sciences of the United States of America · 2006 · 24 citations
    7. Changes of serum trace elements level in patients with alopecia areata: A meta‐analysis Journal of dermatology · 2017 · 23 citations
    8. Serum vitamin D3 level in patients with female pattern hair loss International Journal of Trichology · 2016 · 23 citations
    9. Alpha tocopherol-Nanocellulose loaded alginate membranes and Pluronic hydrogels for diabetic wound healing Materials & Design · 2022 · 22 citations
    10. Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita Journal of Investigative Dermatology · 2012 · 22 citations
    11. Factors associated with anti-SARS-CoV-2 IgG antibody production in patients convalescing from COVID-19 Journal of infection and chemotherapy · 2021 · 21 citations
    12. Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis PLoS ONE · 2014 · 21 citations
    13. Hair Minerals and Metabolic Health in Belgian Elementary School Girls Biological Trace Element Research · 2012 · 21 citations
    14. Androgens stimulate specific aspects of maternal nest-building and reduce food intake in rabbits Hormones and Behavior · 2003 · 21 citations
    15. Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome Genes · 2019 · 20 citations
    16. High‐frequency (22‐MHz) ultrasound for assessing the depth of basal cell carcinoma invasion Skin Research and Technology · 2021 · 18 citations
    17. The Inhibition Activity of Tannin on the Formation of Mono-Species and Polymicrobial Biofilm Escherichia coli, Staphylococcus aureus, Pseudomonas aeruginosa, and Candida albicans Majalah Obat Tradisional · 2019 · 17 citations
    18. Topical minoxidil for extended areate alopecia Acta Dermato Venereologica · 1985 · 17 citations
    19. Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript Experimental Dermatology · 2010 · 14 citations
    20. A second <i>KRT</i>71 allele in curly coated dogs Animal Genetics · 2018 · 13 citations
    21. Economic Burden and Healthcare Resource Use of Alopecia Areata in an Insured Population in the USA Dermatology and therapy · 2022 · 12 citations
    22. The anxiolytic-like effects of estazolam on a PTSD animal model Psychiatry research · 2018 · 12 citations
    23. Novel missense mutation in the EDA gene in a family affected by oligodontia 2016 · 12 citations
    24. Scalp involvement in pemphigus: a prognostic marker Advances in Dermatology and Allergology · 2017 · 10 citations
    25. Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene Journal of Molecular Neuroscience · 2022 · 9 citations
    26. Epigenetic Effects of Gender-Affirming Hormone Treatment: A Pilot Study of the ESR2 Promoter’s Methylation in AFAB People Biomedicines · 2022 · 9 citations
    27. <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology Journal of dermatology · 2020 · 9 citations
    28. Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review The Journal of Dermatology · 2018 · 9 citations
    29. CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation American journal of ophthalmology. Case reports · 2017 · 9 citations
    30. Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan Genes · 2016 · 9 citations