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Journal Abstract Search

384 related items for PubMed ID: 7524919

  • 21. Epidermolytic hyperkeratosis: a keratin 1 or 10 mutational event.
    Lacz NL, Schwartz RA, Kihiczak G.
    Int J Dermatol; 2005 Jan; 44(1):1-6. PubMed ID: 15663649
    [Abstract] [Full Text] [Related]

  • 22. Epidermolytic hyperkeratosis type PS-1 caused by aberrant splicing of KRT1.
    Tal O, Bergman R, Alcalay J, Indelman M, Sprecher E.
    Clin Exp Dermatol; 2005 Jan; 30(1):64-7. PubMed ID: 15663507
    [Abstract] [Full Text] [Related]

  • 23. Superficial epidermolytic ichthyosis: a report of two families.
    Cervantes T, Pham C, Browning JC.
    Pediatr Dermatol; 2013 Jan; 30(4):469-72. PubMed ID: 22612346
    [Abstract] [Full Text] [Related]

  • 24. Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs.
    Credille KM, Barnhart KF, Minor JS, Dunstan RW.
    Br J Dermatol; 2005 Jul; 153(1):51-8. PubMed ID: 16029326
    [Abstract] [Full Text] [Related]

  • 25. Epidermolytic hyperkeratosis with polycyclic psoriasiform plaques resulting from a mutation in the keratin 1 gene.
    Michael EJ, Schneiderman P, Grossman ME, Christiano AM.
    Exp Dermatol; 1999 Dec; 8(6):501-3. PubMed ID: 10597140
    [Abstract] [Full Text] [Related]

  • 26. A novel asparagine-->aspartic acid mutation in the rod 1A domain in keratin 2e in a Japanese family with ichthyosis bullosa of Siemens.
    Takizawa Y, Akiyama M, Nagashima M, Shimizu H.
    J Invest Dermatol; 2000 Jan; 114(1):193-5. PubMed ID: 10620137
    [Abstract] [Full Text] [Related]

  • 27. A novel threonine --> proline mutation at the end of 2B rod domain in the keratin 2e chain in ichthyosis bullosa of Siemens.
    Yang JM, Lee S, Bang HD, Kim WS, Lee ES, Steinert PM.
    J Invest Dermatol; 1997 Jul; 109(1):116-8. PubMed ID: 9204966
    [Abstract] [Full Text] [Related]

  • 28. Genetic approaches to understanding the keratinopathies.
    Bale SJ, DiGiovanna JJ.
    Adv Dermatol; 1997 Jul; 12():99-113; discussion 114. PubMed ID: 8973737
    [Abstract] [Full Text] [Related]

  • 29. A novel helix termination mutation in keratin 10 in annular epidermolytic ichthyosis, a variant of bullous congenital ichthyosiform erythroderma.
    Suga Y, Duncan KO, Heald PW, Roop DR.
    J Invest Dermatol; 1998 Dec; 111(6):1220-3. PubMed ID: 9856845
    [Abstract] [Full Text] [Related]

  • 30. The molecular genetics of keratin disorders.
    Smith F.
    Am J Clin Dermatol; 2003 Dec; 4(5):347-64. PubMed ID: 12688839
    [Abstract] [Full Text] [Related]

  • 31. Epidermolytic hyperkeratosis and epidermolysis bullosa simplex caused by frameshift mutations altering the v2 tail domains of keratin 1 and keratin 5.
    Sprecher E, Yosipovitch G, Bergman R, Ciubutaro D, Indelman M, Pfendner E, Goh LC, Miller CJ, Uitto J, Richard G.
    J Invest Dermatol; 2003 Apr; 120(4):623-6. PubMed ID: 12648226
    [Abstract] [Full Text] [Related]

  • 32. A unique pattern of dyskeratosis characterizes epidermolytic hyperkeratosis and epidermolytic palmoplantar keratoderma.
    Bergman R, Khamaysi Z, Sprecher E.
    Am J Dermatopathol; 2008 Apr; 30(2):101-5. PubMed ID: 18360110
    [Abstract] [Full Text] [Related]

  • 33. Identification of a novel mutation in keratin 1 in a family with epidermolytic hyperkeratosis.
    Arin MJ, Longley MA, Epstein EH, Rothnagel JA, Roop DR.
    Exp Dermatol; 2000 Feb; 9(1):16-9. PubMed ID: 10688370
    [Abstract] [Full Text] [Related]

  • 34. Identification of a de novo keratin 1 mutation in epidermolytic hyperkeratosis with palmoplantar involvement.
    Math A, Frank J, Handisurya A, Poblete-Gutiérrez P, Slupetzky K, Födinger D, Winter D, Stingl G, Kirnbauer R.
    Eur J Dermatol; 2006 Feb; 16(5):507-10. PubMed ID: 17101470
    [Abstract] [Full Text] [Related]

  • 35. 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
    [Abstract] [Full Text] [Related]

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  • 37. Mutations in the genes for epidermal keratins in epidermolysis bullosa and epidermolytic hyperkeratosis.
    Leigh IM, Lane EB.
    Arch Dermatol; 1993 Dec; 129(12):1571-7. PubMed ID: 7504434
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