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Journal Abstract Search

210 related items for PubMed ID: 2260881

  • 1. Hereditary palmoplantar keratosis of the Gamborg Nielsen type. Clinical and ultrastructural characteristics of a new type of autosomal recessive palmoplantar keratosis.
    Kastl I, Anton-Lamprecht I, Gamborg Nielsen P.
    Arch Dermatol Res; 1990; 282(6):363-70. PubMed ID: 2260881
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  • 2. A comparative histopathological examination of biopsies from patients with either the dominant or the Gamborg Nielsen type of hereditary palmoplantar keratoderma.
    Gamborg Nielsen P, Mölne L.
    Dermatology; 1994; 188(4):333-4. PubMed ID: 8193413
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  • 5. Hereditary palmoplantar keratoderma and dermatophytosis in the northernmost county of Sweden (Norrbotten).
    Nielsen PG.
    Acta Derm Venereol Suppl (Stockh); 1994; 188():1-60. PubMed ID: 9868488
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  • 6. The dominant form of hereditary palmoplantar keratoderma in the northernmost county of Sweden (Norrbotten).
    Gamborg Nielsen P, Hofer PA, Lagerholm B.
    Dermatology; 1994; 188(3):188-93. PubMed ID: 7514461
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  • 11. Two different clinical and genetic forms of hereditary palmoplantar keratoderma in the northernmost county of Sweden.
    Gamborg Nielsen P.
    Clin Genet; 1985 Nov; 28(5):361-6. PubMed ID: 2935332
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  • 12. Diffuse epidermolytic palmoplantar keratoderma (Unna-Thost-).
    Hinterberger L, Pföhler C, Vogt T, Müller CS.
    BMJ Case Rep; 2012 Nov 09; 2012():. PubMed ID: 23144341
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  • 14. Palmar-plantar keratoderma. A clinical, ultrastructural, and biochemical study.
    Sybert VP, Dale BA, Holbrook KA.
    J Am Acad Dermatol; 1988 Jan 09; 18(1 Pt 1):75-86. PubMed ID: 2450111
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  • 16. Malignant melanoma developing in an area of hereditary palmoplantar keratoderma (Mal de Meleda).
    Mozzillo N, Nunziata CA, Caracò C, Fazioli F, Botti G, Melanoma Cooperative Group.
    J Surg Oncol; 2003 Dec 09; 84(4):229-33. PubMed ID: 14756434
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  • 17. 2 Cases of hereditary palmoplantar keratoderma. An abnormality of keratohyalin granules and keratin fibril formation.
    Tezuka T.
    Dermatologica; 1984 Dec 09; 169(3):138-45. PubMed ID: 6207058
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  • 18. Keratosis linearis with ichthyosis congenita and sclerosing keratoderma (KLICK-syndrome): a rare, autosomal recessive disorder of keratohyaline formation?
    Vahlquist A, Pontén F, Pettersson A.
    Acta Derm Venereol; 1997 May 09; 77(3):225-7. PubMed ID: 9188877
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  • 20. Mal de Meleda-like palmoplantar keratoderma.
    Iio T, Shiraishi S, Sayama K, Miki Y.
    J Dermatol; 1991 Jan 09; 18(1):43-6. PubMed ID: 2050907
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