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Journal Abstract Search


293 related items for PubMed ID: 2971584

  • 1.
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  • 2. Hereditary epidermolytic palmoplantar keratoderma (Vörner type) in a family with Ehlers-Danlos syndrome.
    Mofid MZ, Costarangos C, Gruber SB, Koch SE.
    J Am Acad Dermatol; 1998 May; 38(5 Pt 2):825-30. PubMed ID: 9591795
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  • 3. Indication for the identity of palmoplantar keratoderma type Unna-Thost with type Vörner. Thost's family revisited 110 years later.
    Küster W, Becker A.
    Acta Derm Venereol; 1992 May; 72(2):120-2. PubMed ID: 1350396
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  • 5. Hereditary epidermolytic palmoplantar keratoderma (Vörner type). Report of a familial case and review of the literature.
    Kanitakis J, Tsoitis G, Kanitakis C.
    J Am Acad Dermatol; 1987 Sep; 17(3):414-22. PubMed ID: 2958520
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  • 8. Autosomal recessive epidermolytic palmoplantar keratoderma.
    Alsaleh QA, Teebi AS.
    J Med Genet; 1990 Aug; 27(8):519-22. PubMed ID: 2145438
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  • 9. A novel nonepidermolytic palmoplantar keratoderma: a clinical and histopathologic study of six cases.
    Magro CM, Baden LA, Crowson AN, Bowden PE, Baden HP.
    J Am Acad Dermatol; 1997 Jul; 37(1):27-33. PubMed ID: 9216520
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  • 10. Infantile epidermolytic ichthyosis with prominent maternal palmoplantar keratoderma.
    Austin Smith W, Cope A, Fernandez M, Parekh P.
    Dermatol Online J; 2016 Apr 18; 22(4):. PubMed ID: 27617465
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  • 11. [Familial palmo-plantar keratoderma with epidermolytic hyperkeratosis (author's transl)].
    Moulin G, Bouchet R.
    Ann Dermatol Venereol; 1977 Jan 18; 104(1):38-44. PubMed ID: 14586
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  • 12. Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma.
    Navsaria HA, Swensson O, Ratnavel RC, Shamsher M, McLean WH, Lane EB, Griffiths D, Eady RA, Leigh IM.
    J Invest Dermatol; 1995 Mar 18; 104(3):425-9. PubMed ID: 7532198
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  • 14. Hereditary epidermolytic palmoplantar keratoderma associated with breast and ovarian cancer in a large kindred.
    Blanchet-Bardon C, Nazzaro V, Chevrant-Breton J, Espie M, Kerbrat P, Le Marec B.
    Br J Dermatol; 1987 Sep 18; 117(3):363-70. PubMed ID: 2960371
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  • 15. R162W mutation of keratin 9 in a family with autosomal dominant palmoplantar keratoderma with unique histologic features.
    Mayuzumi N, Shigihara T, Ikeda S, Ogawa H.
    J Investig Dermatol Symp Proc; 1999 Sep 18; 4(2):150-2. PubMed ID: 10536990
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  • 16. [Keratoderma with epidermolytic hyperkeratosis].
    Woscoff A, Casas JG, Dancziger E.
    Med Cutan Ibero Lat Am; 1986 Sep 18; 14(4):270-4. PubMed ID: 2946910
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  • 17. A Family with Palmar and Plantar Hyperkeratosis: A Quiz.
    Juratli HA, Jägle S, Happle R, Avci P, Didona D, Fischer J.
    Acta Derm Venereol; 2020 Feb 27; 100(4):adv00064. PubMed ID: 32052849
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  • 18. Two different clinical and genetic forms of hereditary palmoplantar keratoderma in the northernmost county of Sweden.
    Gamborg Nielsen P.
    Clin Genet; 1985 Nov 27; 28(5):361-6. PubMed ID: 2935332
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  • 19. [Keratoses with granular degeneration and their relations to each other. II. Heterophenotypic expression of hyperkeratosis (erythrodermia congenitalis ichthyosiformis bullosa), naevus hystricoides and Vörner keratosis palmoplantaris cum degeneratione granulosa].
    Hadlich J, Linse R.
    Dermatol Monatsschr; 1989 Nov 27; 175(7):418-24. PubMed ID: 2529147
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  • 20. Epidermolytic palmoplantar keratoderma of Vörner: re-evaluation of Vörner's original family and identification of a novel keratin 9 mutation.
    Küster W, Reis A, Hennies HC.
    Arch Dermatol Res; 2002 Aug 27; 294(6):268-72. PubMed ID: 12192490
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