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    Research 571–600 of 1000+

    1. Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development International Journal of Molecular Sciences · 2016 · 14 citations
    2. Complex X chromosome rearrangement associated with multiorgan autoimmunity Molecular cytogenetics · 2015 · 8 citations
    3. Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance? Wiener medizinische Wochenschrift · 2020 · 7 citations
    4. The origins of skin diversity: lessons from dermal fibroblasts Development · 2022 · 6 citations
    5. Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl 2011 · 6 citations
    6. Clinical Presentations and Comorbidities of Pediatric Alopecia Areata Pediatric Dermatology · 2025 · 4 citations
    7. Acne Tarda and Male-Pattern Baldness Unmasking Primary Ovarian Insufficiency: A Case and Review Dermatology · 2014 · 4 citations
    8. Advancements and Applications of Injectable Hydrogel Composites in Biomedical Research and Therapy Gels · 2023 · 2 citations
    9. Collagen Involvement in Health, Disease, and Medicine IntechOpen eBooks · 2022 · 1 citations
    10. A Case Report and a Review of TRAPPC4‐Related TRAPPopathy International Journal of Developmental Neuroscience · 2026
    11. Skin Organoids for Disease Modelling, Drug Screening and Regenerative Medicine: Recent Advances and Future Perspectives Wound Repair and Regeneration · 2026
    12. THE IMPACT OF HOMOCYSTEINE IN LUPUS ERYTHEMATOSUS: A LINK OF INFLAMMATION, SKIN AND CARDIOVASCULAR RISK Academic Medical Journal · 2025
    13. Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy Journal of Investigative Dermatology · 2003 · 52 citations
    14. Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization) Journal of The European Academy of Dermatology and Venereology · 2004 · 22 citations
    15. Association of Sensorineural Hearing Loss in Patients With Alopecia Areata JAMA Dermatology · 2020 · 16 citations
    16. A Survey of Women Polycystic Ovarian Disease (PCOD) Zenodo (CERN European Organization for Nuclear Research) · 2026
    17. A Survey of Women Polycystic Ovarian Disease (PCOD) Zenodo (CERN European Organization for Nuclear Research) · 2026
    18. Polycystic Ovary Syndrome: Pathophysiology, Clinical Manifestations and Emerging Therapeutic Approaches Asian Journal of Pharmacy and Pharmacology · 2026
    19. A case of acrodermatitis enteropathica misdiagnosed as staphylococcal scalded skin syndrome Turkish Journal of Dermatology · 2020
    20. Tricholemmoma and tricholemmal carcinoma and Cowden syndrome 2019
    21. Trichotillomania Triggered by Vitamin D Deficiency and Resolving Dramatically With Vitamin D Therapy Clinical neuropharmacology · 2019
    22. An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis Journal of Investigative Dermatology · 2006 · 97 citations
    23. Transforming growth factor-β in stem cells and tissue homeostasis Bone Research · 2018 · 245 citations
    24. Epidemiology and burden of alopecia areata: a systematic review Clinical, Cosmetic and Investigational Dermatology · 2015 · 144 citations
    25. An X-Linked Gene Involved in Androgenetic Alopecia: A Lesson to Be Learned from Adrenoleukodystrophy Dermatology · 2000 · 24 citations
    26. The efficacy and safety of valproic acid medications with controlled active ingredient release in adults in real clinical practice from the position of pharmacokinetic and pharmacogenetic approaches Nevrologiâ, nejropsihiatriâ, psihosomatika · 2017 · 5 citations
    27. Androgenetic alopecia in women Revista del Centro Dermatológico Pascua · 2007
    28. PSEUDOPELADE: AN INHERITED ALOPECIA International Journal of Dermatology · 1996 · 19 citations
    29. News in brief Expert Review of Dermatology · 2010
    30. Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies Journal of dermatological science · 2023