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Journal Abstract Search

264 related items for PubMed ID: 22336941

  • 1. Keratin 16-null mice develop palmoplantar keratoderma, a hallmark feature of pachyonychia congenita and related disorders.
    Lessard JC, Coulombe PA.
    J Invest Dermatol; 2012 May; 132(5):1384-91. PubMed ID: 22336941
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  • 6. Building models for keratin disorders.
    Koster MI.
    J Invest Dermatol; 2012 May; 132(5):1324-6. PubMed ID: 22499036
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  • 12. A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita.
    Liao H, Sayers JM, Wilson NJ, Irvine AD, Mellerio JE, Baselga E, Bayliss SJ, Uliana V, Fimiani M, Lane EB, McLean WH, Leachman SA, Smith FJ.
    J Dermatol Sci; 2007 Dec; 48(3):199-205. PubMed ID: 17719747
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  • 15. Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16.
    Spaunhurst KM, Hogendorf AM, Smith FJ, Lingala B, Schwartz ME, Cywinska-Bernas A, Zeman KJ, Tang JY.
    Br J Dermatol; 2012 Apr; 166(4):875-8. PubMed ID: 22098151
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  • 17. First case of pachyonychia congenita in the Czech Republic.
    Jiráková A, Rajská L, Rob F, Džambová M, Sečníková Z, Göpfertová D, Schwartz M, Smith F, Lotti T, Hercogová J.
    Dermatol Ther; 2015 Apr; 28(1):10-2. PubMed ID: 25174302
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  • 18. Pachyonychia congenita: a case report.
    Kohli N.
    Cutis; 2009 Nov; 84(5):269-71. PubMed ID: 20099620
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  • 19. Generalized bullae in a young girl with KRT6A-related pachyonychia congenita.
    Liu J, Zhong W, Yu B, Lin Z, Zheng Y, Hu X.
    Pediatr Dermatol; 2020 Sep; 37(5):974-976. PubMed ID: 32662074
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  • 20. 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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