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Journal Abstract Search

320 related items for PubMed ID: 15840119

  • 1. A severe case of pachyonychia congenita type I due to a novel proline mutation in keratin 6a.
    García-Rio I, Peñas PF, García-Díez A, McLean WH, Smith FJ.
    Br J Dermatol; 2005 Apr; 152(4):800-2. PubMed ID: 15840119
    [No Abstract] [Full Text] [Related]

  • 2. Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2.
    Celebi JT, Tanzi EL, Yao YJ, Michael EJ, Peacocke M.
    J Invest Dermatol; 1999 Nov; 113(5):848-50. PubMed ID: 10571744
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  • 3. Keratin 17 mutation in pachyonychia congenita type 2 patient with early onset steatocystoma multiplex and Hutchinson-like tooth deformity.
    Oh SW, Kim MY, Lee JS, Kim SC.
    J Dermatol; 2006 Mar; 33(3):161-4. PubMed ID: 16620218
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  • 5. [Type I pachyonychia congenita (Jadarssohn-Lewandowsky)].
    Wimmershoff MB, Stolz W, Schiffner R, Landthaler M.
    Klin Padiatr; 1999 Mar; 211(3):179-83. PubMed ID: 10412130
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  • 6. [Pachyonychia congenita type 2 due to mutation in the keratin 6b gene].
    Toth GG, Van Goor H, McLean WH, Jonkman MF.
    Ned Tijdschr Geneeskd; 2000 Aug 05; 144(32):1563-4. PubMed ID: 10979817
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  • 7. Identification of a recurrent mutation in keratin 6a in a patient with overlapping clinical features of pachyonychia congenita types 1 and 2.
    Ward KM, Cook-Bolden FE, Christiano AM, Celebi JT.
    Clin Exp Dermatol; 2003 Jul 05; 28(4):434-6. PubMed ID: 12823309
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  • 10. [Pachyonychia congenita. Keratin gene mutations with pleiotropic effect].
    Swensson O.
    Hautarzt; 1999 Jul 05; 50(7):483-90. PubMed ID: 10464680
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  • 11. Focal palmoplantar and gingival keratosis: a distinct palmoplantar ectodermal dysplasia with epidermolytic alterations but lack of mutations in known keratins.
    Kolde G, Hennies HC, Bethke G, Reichart PA.
    J Am Acad Dermatol; 2005 Mar 05; 52(3 Pt 1):403-9. PubMed ID: 15761417
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  • 13. A novel keratin 9 gene mutation (Met156Arg) in a Japanese patient with epidermolytic palmoplantar keratoderma.
    Shimazu K, Tsunemi Y, Hattori N, Saeki H, Komine M, Adachi M, Tamaki K.
    Int J Dermatol; 2006 Sep 05; 45(9):1128-30. PubMed ID: 16961539
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  • 20. Novel keratin 17 mutations in pachyonychia congenita type 2.
    Smith FJ, Coleman CM, Bayoumy NM, Tenconi R, Nelson J, David A, McLean WH.
    J Invest Dermatol; 2001 May 05; 116(5):806-8. PubMed ID: 11348474
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