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    Research 121–150 of 1000+

    1. Clinical and Genetic Aspects of Alopecia Areata: A Cutting Edge Review Genes · 2023 · 1 citations
    2. British Association of Dermatologists living guideline for managing people with alopecia areata 2025 British Journal of Dermatology · 2025
    3. Comprehensive Review on Hair Loss and Restorative Techniques: Advances in Diagnostic, Artistry, and Surgical Innovation Cureus · 2025
    4. Non‐biologic immunosuppressive drugs for inflammatory and autoimmune skin diseases Journal der Deutschen Dermatologischen Gesellschaft · 2024
    5. Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System 2019 · 142 citations
    6. Ovarian steroid cell tumor in a teenager masquerading as polycystic ovary syndrome: a case report and literature review Journal of Ovarian Research · 2025
    7. First Symposium of Ichthyosis Experts 2013 · 1 citations
    8. Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration International Journal of Molecular Sciences · 2026
    9. Skin Appendage Proteins of Tetrapods: Building Blocks of Claws, Feathers, Hair and Other Cornified Epithelial Structures Animals · 2025
    10. Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata) Journal of Cutaneous Pathology · 2025
    11. Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control Experimental dermatology · 2005 · 20 citations
    12. A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2 Revista Paulista de Pediatria · 2023
    13. A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child Clinical dermatology review · 2022
    14. Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma British Journal of Dermatology · 2011 · 11 citations
    15. Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn Cureus · 2023 · 1 citations
    16. British Hair and Nail Society British Journal of Dermatology · 2016 · 1 citations
    17. Unruly hair British Journal of Dermatology · 1985 · 19 citations
    18. Ichthyosis American journal of clinical dermatology · 2003 · 147 citations
    19. New developments in the molecular treatment of ichthyosis: review of the literature Orphanet journal of rare diseases · 2022 · 21 citations
    20. A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome Annals of Dermatology · 2022 · 1 citations
    21. Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report Clinical Cosmetic and Investigational Dermatology · 2023
    22. Androgen excess and post-reproductive health Maturitas · 2018 · 10 citations
    23. Adrenal causes of endocrine hypertension in childhood or adolescence Journal of Endocrinological Investigation · 2025
    24. Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse HAL (Le Centre pour la Communication Scientifique Directe) · 2014
    25. What does acne genetics teach us about disease pathogenesis? British Journal of Dermatology · 2019 · 29 citations
    26. Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection Biomedicines · 2025
    27. Ptosis in childhood Medicine · 2018 · 15 citations
    28. Alopecia. International Journal of Dermatology · 1980 · 22 citations
    29. Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention Photodermatology Photoimmunology & Photomedicine · 2020 · 6 citations
    30. Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene 2001 · 139 citations