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    Research 631–660 of 1000+

    1. Anticonvulsant-Induced Cutaneous Reactions CNS Drugs · 1999 · 18 citations
    2. Considerations in genetic counseling of transgender patients: Cultural competencies and altered disease risk profiles Journal of Genetic Counseling · 2020 · 17 citations
    3. Ethnic Hair Disorders Current problems in dermatology · 2015 · 17 citations
    4. Hair Tourniquet Syndrome of the Toe: Report of 2 New Cases Journal of Pediatric Orthopaedics · 2009 · 17 citations
    5. A Case of Kerion Celsi Caused by Microsporum gypseum (Arthroderma gypseum ) in a Child Nippon Ishinkin Gakkai Zasshi · 2009 · 17 citations
    6. Association of type 2 diabetes with central-scalp hair loss in a large cohort study of African American women International Journal of Women's Dermatology · 2019 · 16 citations
    7. New changes in pregnancy and lactation labelling: Review of dermatologic drugs International Journal of Women's Dermatology · 2019 · 16 citations
    8. Alopecia Areata of the Beard: A Review of the Literature American Journal of Clinical Dermatology · 2017 · 16 citations
    9. Case 21-2012 The New England Journal of Medicine · 2012 · 16 citations
    10. Congenital adrenal hyperplasia Dermatologic Therapy · 2008 · 16 citations
    11. “Cold” X5 Hairlaser™ used to treat male androgenic alopecia and hair growth: an uncontrolled pilot study BMC Research Notes · 2014 · 15 citations
    12. Hair follicle development and related gene and protein expression of skins in Rex rabbits during the first 8 weeks of life Asian-Australasian Journal of Animal Sciences · 2018 · 14 citations
    13. Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain 2018 · 14 citations
    14. Primary cutaneous follicle centre cell lymphoma of the scalp presenting with scarring alopecia British Journal of Dermatology · 2011 · 13 citations
    15. Novel missense mutation in the EDA gene in a family affected by oligodontia 2016 · 12 citations
    16. A Comprehensive Approach to Hair Pathology of Horizontal Sections The American Journal of Dermatopathology · 2013 · 12 citations
    17. Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature BMC pediatrics · 2020 · 11 citations
    18. Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation American Journal of Medical Genetics - Part A · 2010 · 11 citations
    19. Wild geladas (Theropithecus gelada) in crops—more than in pasture areas—reduce aggression and affiliation Primates · 2021 · 10 citations
    20. Biotinidase deficiency characterized by skin and hair findings Clinics in Dermatology · 2020 · 10 citations
    21. Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese PLoS ONE · 2015 · 10 citations
    22. Carboxytherapy in Aesthetic Medicine Springer eBooks · 2011 · 10 citations
    23. Out/Performing Our Selves: Invitation for Dialogue Sexualities · 2002 · 10 citations
    24. 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
    25. Rice bran mineral extract increases the expression of anagen-related molecules in human dermal papilla through wnt/catenin pathway Food & Nutrition Research · 2017 · 9 citations
    26. Multiple minute digitate hyperkeratosis Journal of the European Academy of Dermatology and Venereology · 2002 · 9 citations
    27. Familial frontal fibrosing alopecia: A cross‐sectional study of 20 cases from nine families Australasian Journal of Dermatology · 2018 · 8 citations
    28. Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability European Journal of Pediatrics · 2008 · 8 citations
    29. Dexpanthenol may be a novel treatment for male androgenetic alopecia: Analysis of nine cases Dermatologic Therapy · 2020 · 7 citations
    30. Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum Neurodegenerative Diseases · 2018 · 7 citations