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Journal Abstract Search

158 related items for PubMed ID: 20470930

  • 1. [Keratin k6c mutations in focal palmoplantar keratoderma].
    Dereure O.
    Ann Dermatol Venereol; 2010 May; 137(5):423-4. PubMed ID: 20470930
    [No Abstract] [Full Text] [Related]

  • 2. Mutations in a keratin 6 isomer (K6c) cause a type of focal palmoplantar keratoderma.
    Bowden PE.
    J Invest Dermatol; 2010 Feb; 130(2):336-8. PubMed ID: 20081885
    [Abstract] [Full Text] [Related]

  • 3. A novel frameshift mutation in keratin 16 underlies pachyonychia congenita with focal palmoplantar keratoderma.
    Cao LH, Luo Y, Wen W, Liu WL, Jiang L, Chen C, Ji CY, Zhang X.
    Br J Dermatol; 2011 Nov; 165(5):1145-7. PubMed ID: 21668426
    [No Abstract] [Full Text] [Related]

  • 4. Thick nails, plantar keratoderma, follicular hyperkeratosis, and leukokeratosis associated with a novel mutation in KRT6A gene.
    Tous-Romero F, Vico-Alonso C, Calleja-Algarra A, Sánchez-Calvín MT, Palencia-Pérez S.
    Int J Dermatol; 2019 Apr; 58(4):E89-E90. PubMed ID: 30515758
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  • 7. A new KRT16 mutation associated with a phenotype of pachyonychia congenita.
    Paris F, Hurtado C, Azón A, Aguado L, Vizmanos JL.
    Exp Dermatol; 2013 Dec; 22(12):838-9. PubMed ID: 24118415
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  • 8. Two novel de novo mutations of KRT6A and KRT16 genes in two Chinese pachyonychia congenita pedigrees with fissured tongue or diffuse plantar keratoderma.
    Du ZF, Xu CM, Zhao Y, Liu WT, Chen XL, Chen CY, Fang H, Ke HP, Zhang XN.
    Eur J Dermatol; 2012 Dec; 22(4):476-80. PubMed ID: 22668561
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  • 13. Keratin K6c mutations cause focal palmoplantar keratoderma.
    Wilson NJ, Messenger AG, Leachman SA, O'Toole EA, Lane EB, McLean WH, Smith FJ.
    J Invest Dermatol; 2010 Feb; 130(2):425-9. PubMed ID: 19609311
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  • 15. Identification of clinically useful predictive genetic variants in pachyonychia congenita.
    Samuelov L, Sarig O, Adir N, Pavlovsky M, Smith FJ, Schwartz J, Hansen CD, Sprecher E.
    Clin Exp Dermatol; 2021 Jul; 46(5):867-873. PubMed ID: 33486795
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  • 17. Genotype‒Structurotype‒Phenotype Correlations in Patients with Pachyonychia Congenita.
    Wu TT, Eldirany SA, Bunick CG, Teng JMC.
    J Invest Dermatol; 2021 Dec; 141(12):2876-2884.e4. PubMed ID: 34116063
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  • 18. [The 521 T--> C mutation in the keratin 6A gene in a pedigree with pachyonychia congenita type I].
    Yang L, Li M, Lai M, Ni J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Feb; 27(1):66-8. PubMed ID: 20140871
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  • 19. Pachyonychia congenita: a case report of a successful treatment with rosuvastatin in a patient with a KRT6A mutation.
    Abdollahimajd F, Rajabi F, Shahidi-Dadras M, Saket S, Youssefian L, Vahidnezhad H, Uitto J.
    Br J Dermatol; 2019 Sep; 181(3):584-586. PubMed ID: 30307612
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  • 20. Revisiting pachyonychia congenita: a case-cohort study of 815 patients.
    Samuelov L, Smith FJD, Hansen CD, Sprecher E.
    Br J Dermatol; 2020 Mar; 182(3):738-746. PubMed ID: 31823354
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