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    Research 31–60 of 387

    1. Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature Jaypee's international journal of clinical pediatric dentistry · 2018 · 11 citations
    2. Lichen Spinulosus: Case Report and Review of Literatures JOURNAL OF HEALTH SCIENCE · 2015 · 11 citations
    3. Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis Journal of Investigative Dermatology · 2016 · 8 citations
    4. A newborn presenting with congenital blistering International Journal of Dermatology · 2004 · 7 citations
    5. Building Models for Keratin Disorders 2012 · 4 citations
    6. KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies European journal of human genetics · 2022 · 3 citations
    7. Follicular cysts and hyperkeratoses in early mycosis fungoides International Journal of Dermatology · 1998 · 3 citations
    8. Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma British Journal of Dermatology · 2013 · 2 citations
    9. NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis Revista română de medicină de laborator · 2016 · 1 citations
    10. Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders 2012 · 1 citations
    11. When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma Indian Dermatology Online Journal · 2025
    12. Ectodermal Dysplasia: Variable Expressions Indian Journal of Dermatology · 2025
    13. Surgical Management of Severe Cicatricial Ectropion Secondary to Pityriasis Rubra Pilaris. Dermatologic Surgery · 2025
    14. Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma Frontiers in Oncology · 2024
    15. Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report Clinical Cosmetic and Investigational Dermatology · 2023
    16. Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations Indian Journal of Paediatric Dermatology · 2022
    17. Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity Pediatrics in review · 2021
    18. Clouston’s Syndrome-A Case Report Annals of King Edward Medical University · 2021
    19. KRT16 wt Allele Definitions · 2020
    20. Cirmcumscribed juvenile pityriasis rubra pilaris in a 5-year-old-girl treated with topical keratolytic and steroid Journal of The American Academy of Dermatology · 2018
    21. STUDY OF CUTANEOUS MANIFESTATIONS IN THYROID DISORDERS Journal of evolution of medical and dental sciences · 2016
    22. Disorders of Keratinization 2014
    23. Woolly Hair in Two Siblings International Journal of Trichology · 2012
    24. Olmsted syndrome Journal of Dermatological Case Reports · 2013 · 2 citations
    25. Dysfunction of keratinocyte adhesion Experimental Dermatology · 2004 · 2 citations
    26. P029 A case of atypical bullous pemphigoid British Journal of Dermatology · 2026
    27. Pityriasis rubra pilaris: a rare inflammatory dermatosis BMJ case reports · 2018
    28. PA05 A rare case of cardiocutaneous syndrome in a young child 2023
    29. Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation Case reports in dermatological medicine · 2023
    30. [Acitretine]. PubMed · 2001 · 1 citations