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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

264 related items for PubMed ID: 21856558

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  • 2. [Epidermolysis bullosa simplex Dowling-Meara].
    Frangu M, Gedde-Dahl T, Verder H.
    Ugeskr Laeger; 2006 Nov 27; 168(48):4222-4. PubMed ID: 17147951
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  • 4. Keratin mutations in patients with epidermolysis bullosa simplex: correlations between phenotype severity and disturbance of intermediate filament molecular structure.
    Jerábková B, Marek J, Bucková H, Kopecková L, Veselý K, Valícková J, Fajkus J, Fajkusová L.
    Br J Dermatol; 2010 May 27; 162(5):1004-13. PubMed ID: 20030639
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  • 5. Dyskeratosis as a histologic feature in epidermolysis bullosa simplex-Dowling Meara.
    Bergman R, Harel A, Sprecher E.
    J Am Acad Dermatol; 2007 Sep 27; 57(3):463-6. PubMed ID: 17707151
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  • 10. Epidermolysis bullosa nevus arising in a patient with Dowling-Meara type epidermolysis bullosa simplex with a novel K5 mutation.
    Sugiyama-Fukamatsu H, Suzuki N, Nakanishi G, Iwatsuki K.
    J Dermatol; 2009 Aug 27; 36(8):447-52. PubMed ID: 19691749
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  • 11. Ultrastructural findings in epidermolysis bullosa.
    Smith LT.
    Arch Dermatol; 1993 Dec 27; 129(12):1578-84. PubMed ID: 7504435
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  • 12. Laryngeal involvement in the Dowling-Meara variant of epidermolysis bullosa simplex with keratin mutations of severely disruptive potential.
    Shemanko CS, Horn HM, Keohane SG, Hepburn N, Kerr AI, Atherton DJ, Tidman MJ, Lane EB.
    Br J Dermatol; 2000 Feb 27; 142(2):315-20. PubMed ID: 10730767
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  • 14. Epidermolysis bullosa simplex in Japanese and Korean patients: genetic studies in 19 cases.
    Yasukawa K, Sawamura D, Goto M, Nakamura H, Jung SY, Kim SC, Shimizu H.
    Br J Dermatol; 2006 Aug 27; 155(2):313-7. PubMed ID: 16882168
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  • 15. Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex.
    García M, Santiago JL, Terrón A, Hernández-Martín A, Vicente A, Fortuny C, De Lucas R, López JC, Cuadrado-Corrales N, Holguín A, Illera N, Duarte B, Sánchez-Jimeno C, Llames S, García E, Ayuso C, Martínez-Santamaría L, Castiglia D, De Luca N, Torrelo A, Mechan D, Baty D, Zambruno G, Escámez MJ, Del Río M.
    Br J Dermatol; 2011 Sep 27; 165(3):683-92. PubMed ID: 21623745
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  • 17. The clinical spectrum of epidermolysis bullosa simplex.
    Horn HM, Tidman MJ.
    Br J Dermatol; 2000 Mar 27; 142(3):468-72. PubMed ID: 10735952
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  • 18. Epidermolysis bullosa simplex in Scotland caused by a spectrum of keratin mutations.
    Rugg EL, Horn HM, Smith FJ, Wilson NJ, Hill AJ, Magee GJ, Shemanko CS, Baty DU, Tidman MJ, Lane EB.
    J Invest Dermatol; 2007 Mar 27; 127(3):574-80. PubMed ID: 17039244
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  • 20. Three severe cases of EBS Dowling-Meara caused by missense and frameshift mutations in the keratin 14 gene.
    Titeux M, Mazereeuw-Hautier J, Hadj-Rabia S, Prost C, Tonasso L, Fraitag S, de Prost Y, Hovnanian A, Bodemer C.
    J Invest Dermatol; 2006 Apr 27; 126(4):773-6. PubMed ID: 16439965
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