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Journal Abstract Search

250 related items for PubMed ID: 10053007

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  • 7. Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene.
    Cserhalmi-Friedman PB, Squeo R, Gordon D, Garzon M, Schneiderman P, Grossman ME, Christiano AM.
    Clin Exp Dermatol; 2000 May; 25(3):241-3. PubMed ID: 10844506
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  • 8. Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 gene.
    Terron-Kwiatkowski A, Terrinoni A, Didona B, Melino G, Atherton DJ, Irvine AD, McLean WH.
    Br J Dermatol; 2004 Jun; 150(6):1096-103. PubMed ID: 15214894
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  • 11. Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma: possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband.
    Nomura K, Umeki K, Hatayama I, Kuronuma T.
    Arch Dermatol; 2001 Sep; 137(9):1192-5. PubMed ID: 11559215
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  • 12. A keratin 10 gene mutation (Arg156Cys) in a Japanese patient with bullous congenital ichthyosiform erythroderma.
    Saeki H, Hattori N, Mitsui H, Adachi M, Imakado S, Ishibashi Y, Tamaki K.
    J Dermatol; 2002 Mar; 29(3):168-71. PubMed ID: 11990254
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  • 14. A novel substitution in keratin 10 in epidermolytic hyperkeratosis.
    Arin MJ, Longley MA, Anton-Lamprecht I, Kurze G, Huber M, Hohl D, Rothnagel JA, Roop DR.
    J Invest Dermatol; 1999 Apr; 112(4):506-8. PubMed ID: 10201536
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  • 15. Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma).
    Ishida-Yamamoto A, McGrath JA, Judge MR, Leigh IM, Lane EB, Eady RA.
    J Invest Dermatol; 1992 Jul; 99(1):19-26. PubMed ID: 1376754
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  • 16. A keratin K10 gene mutation in a Japanese patient with epidermolytic hyperkeratosis.
    Nomura K, Meng X, Umeki K, Tamai K, Sawamura D, Hashimoto I, Kikuchi T.
    Jpn J Hum Genet; 1997 Mar; 42(1):217-23. PubMed ID: 9184002
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  • 17. Annular epidermolytic ichthyosis with palmoplantar keratosis: a unique phenotype associated with interfamilial phenotypic heterogeneity.
    Liang B, Yuan T, Zhou Y, Ding Y, Tang L, Wang F, Wang P, Li H, Zhang Y, Zhu M, Ji Y, Hong X, Zhang X, Zhu Q.
    Eur J Dermatol; 2020 Jun 01; 30(3):294-299. PubMed ID: 32666929
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  • 19. Bullous congenital ichthyosiform erythroderma of Brocq.
    Kucharekova M, Mosterd K, Winnepenninckx V, van Geel M, Sommer A, van Steensel MA.
    Int J Dermatol; 2007 Nov 01; 46 Suppl 3():36-8. PubMed ID: 17973888
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