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    Research 931–960 of 1000+

    1. Psychosomatic aspects of alopecia areata Clinics in Dermatology · 2018 · 20 citations
    2. Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum Neurodegenerative Diseases · 2018 · 7 citations
    3. Absorption of Excess Selenium and Sulfur by Plants and Animals Journal American Society of Mining and Reclamation · 1995 · 7 citations
    4. Treatment of Alopecia Areata with Oral JAK Inhibitor : Focusing on Clinical Outcomes with Baricitinib The Nishinihon Journal of Dermatology · 2022 · 1 citations
    5. Review of the Use of Platelet-Rich Plasma in the Treatment of Alopecia Plastic and Aesthetic Nursing · 2020 · 1 citations
    6. Integrating Psychodermatology and Platelet-Rich Plasma Therapy in Various Dermatological Conditions: A Narrative Review Cureus · 2025
    7. Community Empowerment and Mentality as a Treatment in Treatment-Resistant Trichotillomania: A Case Report Cureus · 2024
    8. Investigation of Vaspin and Visfatin -4689G/T Gene Polymorphisms in Alopecia Areata Patients OSMANGAZİ JOURNAL OF MEDICINE · 2024
    9. Self-esteem and body image satisfaction in women with PCOS in the Middle East: Cross-sectional social media study PloS one · 2024
    10. A Retrospective Analysis from Turkey: The Effect of the COVID-19 Outbreak Quarantine on Dermatology Outpatient Clinics Journal of the turkish academy of dermatology · 2022
    11. Pubic to Scalp F.U.E. Hair Transplant for Transgender 2021
    12. Vaccines, Infections, and Alopecia Areata 2015
    13. Providing mesotherapy to prevent and treat hair loss in aesthetic practice Journal of Aesthetic Nursing · 2014
    14. Multiomic Characterization of Treatment Response to JAK Inhibition in Patients with APECED Journal of Human Immunity · 2026
    15. A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients Journal of Investigative Dermatology · 1998 · 34 citations
    16. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis Nature Genetics · 2009 · 181 citations
    17. Gene detection in a family with monilethrix and treatment with 5% topical minoxidil Skin research and technology · 2022 · 2 citations
    18. Diseases of Hair and Nails 2025
    19. Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex Veterinary Pathology · 2023 · 2 citations
    20. A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report Revista Paulista de Pediatria · 2024 · 2 citations
    21. Promotion of homology-directed DNA repair by polyamines Nature communications · 2019 · 47 citations
    22. The Role of EAAT4 in Epidermal Differentiation and Calcium Homeostasis during Aging 2023
    23. The dermatoscope in the hair clinic: Trichoscopy of scarring and nonscarring alopecia Journal of the American Academy of Dermatology · 2023 · 24 citations
    24. Clinical and dermatoscopic features of temporal triangular alopecia in infants Skin research and technology · 2023 · 2 citations
    25. Recovery Effects of Oral Supplementation with Polar Lipid-Rich Wheat Extracts on Acute Telogen Effluvium: A Randomized Double-Blind Placebo-Controlled Study Clinical Cosmetic and Investigational Dermatology · 2025
    26. Enhancement of skin rejuvenation and hair growth through novel near-infrared light emitting diode (nNIR) lighting: in vitro and in vivo study Lasers in medical science · 2024
    27. Alopecia areata and Down syndrome: A true association and the importance of dermoscopic diagnosis Journal of The American Academy of Dermatology · 2016
    28. Society for Endocrinology guidelines for testosterone replacement therapy in male hypogonadism Clinical Endocrinology · 2021 · 39 citations
    29. Pathology of Mouse Models of Accelerated Aging Veterinary pathology · 2016 · 81 citations
    30. A missense mutation in the type II hair keratin hHb3 is associated with monilethrix Journal of Medical Genetics · 2005 · 79 citations