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    Research 271–300 of 788

    1. Trichothiodystrophy Associated with Urologic Malformation and Primary Hypercalduria Pediatric Dermatology · 1997 · 7 citations
    2. Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention Photodermatology Photoimmunology & Photomedicine · 2020 · 6 citations
    3. Skin Manifestations of Hypothyroidism-A Clinical Study IOSR Journal of Dental and Medical Sciences · 2013 · 6 citations
    4. Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants 2021 · 6 citations
    5. A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response American Journal of Medical Genetics Part A · 2021 · 5 citations
    6. [Cutaneous manifestations of malabsorption diseases (author's transl)]. PubMed · 1978 · 5 citations
    7. Collodion baby case series: the success of oral retinoic acid Türk pediatri arşivi : İstanbul çocuk kliniği dergisi · 2018 · 4 citations
    8. [Netherton's syndrome in two sisters]. PubMed · 2002 · 3 citations
    9. Trichothiodystrophy without associated neuroectodermal features in two siblings International Journal of Trichology · 2018 · 2 citations
    10. A STUDY ON CUTANEOUS MANIFESTATIONS OF HYPOTHYROIDISM IN A TERTIARY HOSPITAL IN SOUTH INDIA Journal of Evolution of Medical and Dental Sciences · 2015 · 2 citations
    11. Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions International journal of molecular sciences · 2023 · 2 citations
    12. LEKTI: Netherton Syndrome and Atopic Dermatitis InTech eBooks · 2013 · 1 citations
    13. Gene Therapy: Recent Advances and Applications in Dermatology Journal of Cutaneous Medicine and Surgery · 1996 · 1 citations
    14. FilaggrinHigh melanomas exhibit active FGFR and allergic signatures with impaired GNA14 and Th1 signatures Frontiers in Genetics · 2025 · 1 citations
    15. Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders 2012 · 1 citations
    16. Central Precocious Puberty and Sjogren-Larsson Syndrome in a Child: A Rare Case Report Clinical Cosmetic and Investigational Dermatology · 2026
    17. PA11 A rare case of a severe papulopustular dermatosis secondary to a germline <i>EGFR</i> mutation British Journal of Dermatology · 2026
    18. 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
    19. ИХТИОЗ АРЛЕКИНО: КЛИНИЧЕСКИЙ СЛУЧАЙ 2026
    20. Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata) Journal of Cutaneous Pathology · 2025
    21. Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments. PubMed · 2025
    22. Caracterización de signos cutáneos y sus anexos, en niños menores de 5 años con desnutrición severa Revista Digital de Postgrado · 2025
    23. Severe Hypernatremia as Presentation of Netherton Syndrome Global Medical Genetics · 2023
    24. Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report Indian dermatology online journal · 2023
    25. Genes of Congenital Dermatologic Disorders in Dogs—A Review Folia veterinaria · 2021
    26. Relationship between the level of vitamin D in bloof flow and skin dermatosis Rossiiskii Zhurnal Kozhnykh i Venericheskikh Boleznei · 2021
    27. Miscellaneous Skin Diseases Clinical Small Animal Internal Medicine · 2020
    28. Quoi de neuf en dermatologie pédiatrique ? Annales de dermatologie et de vénéréologie · 2017
    29. Mykogene und piläre Faktoren des Haarabbaus durch Dermatomyzeten* (2. Mitteilung) Mycoses · 2009
    30. Secondary Cicatricial and other Permanent Alopecias Springer eBooks · 2008