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    Research 30 of 158

    1. Alopecia Universalis, Onychodystrophy, and Total Vitiligo Archives of Dermatology · 1963 · 31 citations
    2. Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy JAAD Case Reports · 2019 · 4 citations
    3. Onychodystrophy With Associated Polymicrobial Distal Phalanx Osteomyelitis Archives of Dermatology · 2011 · 1 citations
    4. 0447 Minoxidil for onychodystrophy: Can this hair loss remedy be a nail growth remedy? Journal of Investigative Dermatology · 2025
    5. A patient with Cronkhite-Canada syndrome whose entire digestive tracts was examined endoscopically Progress of Digestive Endoscopy · 2014
    6. Juvenile versus maturity-onset alopecia areata- a comparative retrospective clinical study Clinical and Experimental Dermatology · 1989 · 164 citations
    7. Immune-related alopecia (areata and universalis) in cancer patients receiving immune checkpoint inhibitors 2016 · 87 citations
    8. Cutaneous Reactions to Chemotherapeutic Agents ˜The œAmerican journal of the medical sciences · 2001 · 53 citations
    9. Spontaneous improvement of Cronkhite-Canada syndrome in a postpartum female Digestive diseases and sciences · 1984 · 19 citations
    10. Cronkhite-Canada Syndrome (CCS)—A Rare Case Report JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH · 2015 · 17 citations
    11. Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene Yonsei Medical Journal · 2018 · 13 citations
    12. Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review Indian Journal of Dermatology · 2016 · 13 citations
    13. Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder Indian dermatology online journal · 2013 · 12 citations
    14. A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy Case reports in nephrology and dialysis · 2018 · 6 citations
    15. Case of Cronkhite Canada syndrome shows improvement with enteral supplements. PubMed · 2012 · 6 citations
    16. Dermatological concerns for women and girls with turner syndrome Frontiers in Medicine · 2023 · 5 citations
    17. Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i> The Journal of Dermatology · 2017 · 5 citations
    18. Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association Nepalese journal of ophthalmology · 2015 · 5 citations
    19. Cronkhite-Canada Syndrome: an unusual finding of gastro-intestinal adenomatous polyps in a syndrome characterized by hamartomatous polyps Gastroenterology report · 2014 · 5 citations
    20. Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome Case Reports in Clinical Medicine · 2014 · 2 citations
    21. Olmsted syndrome Journal of Dermatological Case Reports · 2013 · 2 citations
    22. Nearly complete hair re-pigmentation in an older patient treated with hydroxyurea for essential thrombocytosis Journal of Oncology Pharmacy Practice · 2024 · 1 citations
    23. Cronkhite-Canada syndrome: A rare disease presenting with dermatological and gastrointestinal manifestations Australasian Journal of Dermatology · 2015 · 1 citations
    24. Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia Our Dermatology Online · 2025
    25. Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis Gastroenterology · 2025
    26. Diffuse Gastrointestinal Polyposis With Skin, Hair, and Nail Changes Gastroenterology · 2022
    27. The features of onychomatrimas on in vivo reflectance confocal microscopy Journal of The American Academy of Dermatology · 2014
    28. A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia 2020 · 2 citations
    29. [Two cases of the rare Cronkhite-Canada syndrome]. PubMed · 2017 · 1 citations
    30. The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant Gene · 2014 · 11 citations