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    Research 331–360 of 536

    1. Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis. PubMed · 1997 · 27 citations
    2. The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i> JAMA dermatology · 2014 · 22 citations
    3. New developments in the molecular treatment of ichthyosis: review of the literature Orphanet journal of rare diseases · 2022 · 21 citations
    4. Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes American Journal of Medical Genetics Part A · 2021 · 16 citations
    5. Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature 2020 · 15 citations
    6. Hodgkin′s lymphoma presenting as alopecia International Journal of Trichology · 2012 · 14 citations
    7. AN UPDATE OF HAIR SHAFT DISORDERS Dermatologic clinics · 1996 · 12 citations
    8. Kaposi varicelliform eruption Indian Dermatology Online Journal · 2015 · 9 citations
    9. Alopecia areata after mogamulizumab treatment JAAD Case Reports · 2021 · 7 citations
    10. <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy Veterinary medicine and science · 2019 · 7 citations
    11. Ichthyosis hystrix Indian dermatology online journal · 2013 · 7 citations
    12. Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention Photodermatology Photoimmunology & Photomedicine · 2020 · 6 citations
    13. Off-label uses of retinoids in dermatology Our Dermatology Online · 2012 · 6 citations
    14. Dermoscopy and Trichoscopy in Dermatomyositis—A Cross-Sectional Study Journal of Clinical Medicine · 2022 · 5 citations
    15. Follicular unit extraction [FUE] – One procedure, many uses Indian Dermatology Online Journal · 2021 · 3 citations
    16. Improvement of Skin Lesions in an Adult with CHILD Syndrome Treated with 2% Ketoconazole Cream Acta Dermato Venereologica · 2024 · 2 citations
    17. SARS-CoV-2 Infection—A Trigger Factor for Telogen Effluvium: Review of the Literature with a Case-Based Guidance for Clinical Evaluation Life · 2023 · 2 citations
    18. Prolonged Drug-Induced Hypersensitivity Syndrome/DRESS With Alopecia Areata and Autoimmune Thyroiditis Federal Practitioner · 2022 · 2 citations
    19. Successful management of Netherton syndrome using IVIG and dupilumab: A case report Journal of Allergy and Clinical Immunology Global · 2025 · 1 citations
    20. Alopecia areata-like presentations with mogamulizumab therapy JAAD case reports · 2023 · 1 citations
    21. Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders Journal of nutrition & health · 2015 · 1 citations
    22. Mycosis Fungoides in Elderly Adults—A Diagnostic Challenge Journal of the American Geriatrics Society · 2014 · 1 citations
    23. LEKTI: Netherton Syndrome and Atopic Dermatitis InTech eBooks · 2013 · 1 citations
    24. Momentary fluke of cyclosporine in incidental repigmentation and hypertrichosis of hair Cosmoderma · 2026
    25. Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management Dermatologic Therapy · 2026
    26. Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis International Journal of Women’s Dermatology · 2024
    27. Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs Frontiers in pharmacology · 2023
    28. “Degeneration” in Dermatopathology Indian journal of dermatology, venereology, and leprology · 2023
    29. Co-Expression Pattern of Artemis Serine 516 Phosphorylation with Indicators Involving in Differentiation, Proliferation and Apoptosis of Human Anagen Hair Follicles: An Immunofluorescence Double-Staining Study Frontiers in bioscience · 2023
    30. Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient International journal of dermatology and venereology · 2022