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    Research 181–210 of 1000+

    1. PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation British Journal of Dermatology · 2026
    2. Long-read RNA sequencing reveals extensive transcript isoform changes in a patient with IFAP syndrome with a recurrent intronic MBTPS2 variant Human Genome Variation · 2026
    3. ИХТИОЗ АРЛЕКИНО: КЛИНИЧЕСКИЙ СЛУЧАЙ 2026
    4. Presentations of Cutaneous Disease in Various Skin Pigmentations: Keratosis Pilaris HCA Healthcare Journal of Medicine · 2026
    5. Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images Clinical Case Reports · 2025
    6. Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome Indian Journal of Paediatric Dermatology · 2025
    7. Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata) Journal of Cutaneous Pathology · 2025
    8. Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments. PubMed · 2025
    9. Netherton Syndrome – Responding to Oral Retinoids International Journal of Trichology · 2025
    10. Caracterización de signos cutáneos y sus anexos, en niños menores de 5 años con desnutrición severa Revista Digital de Postgrado · 2025
    11. 371 Hair follicles are critical modulators of skin barrier function Journal of Investigative Dermatology · 2024
    12. Severe Hypernatremia as Presentation of Netherton Syndrome Global Medical Genetics · 2023
    13. Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies Journal of dermatological science · 2023
    14. Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family Acta Scientific Paediatrics · 2023
    15. Dermatological diseases from a genetic perspective Medizinische Genetik · 2023
    16. Keratosis Pilaris Is a Keratinization of Hair Follicles International journal of integrated medical research · 2023
    17. Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report Indian dermatology online journal · 2023
    18. Does dry skin indicate defective epidermal permeability barrier? Chinese Journal of Dermatology · 2022
    19. Genes of Congenital Dermatologic Disorders in Dogs—A Review Folia veterinaria · 2021
    20. Relationship between the level of vitamin D in bloof flow and skin dermatosis Rossiiskii Zhurnal Kozhnykh i Venericheskikh Boleznei · 2021
    21. Miscellaneous Skin Diseases Clinical Small Animal Internal Medicine · 2020
    22. Netherton Syndrome Harper's Textbook of Pediatric Dermatology · 2019
    23. Uso actual de la vitamina D en dermatología Revista Medicina Cutánea Ibero-Latino-Americana · 2019
    24. Congenital and Hereditary Skin Diseases 2018
    25. Congenital and Hereditary Skin Diseases 2018
    26. Quoi de neuf en dermatologie pédiatrique ? Annales de dermatologie et de vénéréologie · 2017
    27. Bamboo Hair Syndrome or Netherton Syndrome - A Case Report IOSR journal of dental and medical sciences · 2017
    28. New possibilities extemporaneous preparation in dermatology - innovative foam base Espumil Dermatologie pro praxi · 2016
    29. Disorders of Keratinization 2014
    30. Genetics Springer eBooks · 2014