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Journal Abstract Search

217 related items for PubMed ID: 7249491

  • 21. [Diagnosis by electron microscopy of recessive dystrophic epidermolysis bullosa].
    Glorio RR, Solari A, Woscoff A.
    Medicina (B Aires); 2000; 60(3):354-6. PubMed ID: 11050816
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  • 22. Evaluation of anchoring fibrils and other components of the dermal-epidermal junction in dystrophic epidermolysis bullosa by a quantitative ultrastructural technique.
    Tidman MJ, Eady RA.
    J Invest Dermatol; 1985 May; 84(5):374-7. PubMed ID: 4039741
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  • 23. Epidermolysis bullosa hereditaria with junctional blistering in an adult.
    Hashimoto I, Schnyder UW, Anton-Lamprecht I.
    Dermatologica; 1976 May; 152(2):72-86. PubMed ID: 939338
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  • 24. Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations.
    McGrath JA, Ashton GH, Mellerio JE, Salas-Alanis JC, Swensson O, McMillan JR, Eady RA.
    J Invest Dermatol; 1999 Sep; 113(3):314-21. PubMed ID: 10469327
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  • 26. Compound heterozygosity for a nonsense mutation and a splice site mutation in the type VII collagen gene (COL7A1) in recessive dystrophic epidermolysis bullosa.
    Tamai K, Ishida-Yamamoto A, Matsuo S, Iizuka H, Hashimoto I, Christiano AM, Uitto J, McGrath JA.
    Lab Invest; 1997 Feb; 76(2):209-17. PubMed ID: 9042157
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  • 29. Ultrastructural studies in epidermolysis bullosa hereditaria. III. Recessive dystrophic types with dermolytic blistering (Hallopeau-Siemens types and inverse type).
    Hashimoto I, Schnyder UW, Anton-Lamprecht I, Gedde-Dahl T, Ward S.
    Arch Dermatol Res (1975); 1976 Aug 27; 256(2):137-50. PubMed ID: 962387
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  • 30. Three Hong Kong Chinese cases of pretibial epidermolysis bullosa: a genodermatosis that can masquerade as an acquired inflammatory disease.
    Tang WY, Lee KC, Chow TC, Lo KK.
    Clin Exp Dermatol; 1999 May 27; 24(3):149-53. PubMed ID: 10354166
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  • 32. Dystrophic epidermolysis bullosa inversa: report of two cases with further correlation between electron microscopic and immunofluorescence studies.
    Lin AN, Smith LT, Fine JD.
    J Am Acad Dermatol; 1995 Aug 27; 33(2 Pt 2):361-5. PubMed ID: 7615886
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  • 33. Dystrophic epidermolysis bullosa inversa: a case report.
    Altomare GF, Polenghi M, Pigatto PD, Nazzaro V, Piattoni F.
    Dermatologica; 1990 Aug 27; 181(2):145-8. PubMed ID: 2173667
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  • 34. [Acquired epidermolysis bullosa. A clinico-pathologic study].
    Rappersberger K, Konrad K, Schenk P, Tappeiner G.
    Hautarzt; 1988 Jun 27; 39(6):355-62. PubMed ID: 3042704
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  • 38. [ON THE CLINICAL PICTURE AND GENETICS OF DOMINANT DYSTROPHIC HEREDITARY EPIDERMOLYSIS BULLOSA].
    SCHNYDER UW, EICHHOFF D.
    Arch Klin Exp Dermatol; 1963 Dec 19; 218():62-90. PubMed ID: 14106978
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  • 39. Generalized atrophic benign epidermolysis bullosa.
    Hintner H, Wolff K.
    Arch Dermatol; 1982 Jun 19; 118(6):375-84. PubMed ID: 7092249
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  • 40. Rapid diagnosis of major variants of congenital epidermolysis bullosa using a monoclonal antibody against collagen type IV.
    Bolte C, Gonzalez S.
    Am J Dermatopathol; 1995 Dec 19; 17(6):580-3. PubMed ID: 8599472
    [Abstract] [Full Text] [Related]

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