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Journal Abstract Search

179 related items for PubMed ID: 22668561

  • 21. Symptomatic mucosal involvement in pachyonychia congenita: challenges in infants and young children.
    Goldberg I, Mashiah J, Kutz A, Derowe A, Warshauer E, Schwartz ME, Smith F, Sprecher E, Hansen CD.
    Br J Dermatol; 2020 Mar; 182(3):708-713. PubMed ID: 31777952
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  • 22. 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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  • 23. Molecular epidemiology of pachyonychia congenita in the Israeli population.
    Pavlovsky M, Peled A, Samuelov L, Malki L, Malovitski K, Assaf S, Mohamad J, Meijers O, Eskin-Schwartz M, Sarig O, Sprecher E.
    Clin Exp Dermatol; 2021 Jun; 46(4):663-668. PubMed ID: 33190296
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  • 24. Genotype-phenotype correlations among pachyonychia congenita patients with K16 mutations.
    Fu T, Leachman SA, Wilson NJ, Smith FJ, Schwartz ME, Tang JY.
    J Invest Dermatol; 2011 May; 131(5):1025-8. PubMed ID: 21160496
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  • 25. Increased pachyonychia congenita severity in patients with concurrent keratin and filaggrin mutations.
    Gruber R, Wilson NJ, Smith FJ, Grabher D, Steinwender L, Fritsch PO, Schmuth M.
    Br J Dermatol; 2009 Dec; 161(6):1391-5. PubMed ID: 19785597
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  • 32. Genotype-phenotype correlations of neurovascular structures on the feet in patients with pachyonychia congenita: A cross-sectional study.
    Tan XL, Thomas BR, Steele L, Schwartz J, Hansen CD, O'Toole EA.
    J Am Acad Dermatol; 2022 Nov; 87(5):1172-1174. PubMed ID: 35245567
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  • 33. Mutation p.Arg127Pro in the 1A Domain of KRT16 Causes Pachyonychia Congenita in Chinese Patient: A Case Report of PC Associated with Acral Melanoma.
    Ge WW, Chen ZM, Chou MW, Ismail F, Chen G, Wu LM, Yang JQ.
    Clin Cosmet Investig Dermatol; 2024 Nov; 17():1111-1116. PubMed ID: 38770089
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  • 34. Keratin 17 Mutations in Four Families from India with Pachyonychia Congenita.
    Agarwala M, Salphale P, Peter D, Wilson NJ, Pulimood S, Schwartz ME, Smith FJD.
    Indian J Dermatol; 2017 Nov; 62(4):422-426. PubMed ID: 28794556
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  • 36. 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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  • 37. Transgrediens pachyonychia congenita (PC): case series of a nonclassical PC presentation.
    Harris K, Hull PR, Hansen CD, Smith FJ, McLean WH, Arbiser JL, Leachman SA.
    Br J Dermatol; 2012 Jan; 166(1):124-8. PubMed ID: 21790523
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  • 40. A novel H1 mutation in keratin 6a in an infant with pachyonychia congenita.
    Luo S, Luo Q, Zhang H, Wan C.
    Indian J Dermatol Venereol Leprol; 2015 Jan; 81(4):385-7. PubMed ID: 26087092
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