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Journal Abstract Search

161 related items for PubMed ID: 2396835

  • 1. 19-DEJ-1, a monoclonal antibody to the hemidesmosome-anchoring filament complex, is the only reliable immunohistochemical probe for all major forms of junctional epidermolysis bullosa.
    Fine JD.
    Arch Dermatol; 1990 Sep; 126(9):1187-90. PubMed ID: 2396835
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  • 2. 19-DEJ-1, a hemidesmosome-anchoring filament complex-associated monoclonal antibody. Definition of a new skin basement membrane antigenic defect in junctional and dystrophic epidermolysis bullosa.
    Fine JD, Horiguchi Y, Couchman JR.
    Arch Dermatol; 1989 Apr; 125(4):520-3. PubMed ID: 2649012
    [Abstract] [Full Text] [Related]

  • 3. Applicability of 19-DEJ-1 monoclonal antibody for the prenatal diagnosis or exclusion of junctional epidermolysis bullosa.
    Fine JD, Holbrook KA, Elias S, Anton-Lamprecht I, Rauskolb R.
    Prenat Diagn; 1990 Apr; 10(4):219-29. PubMed ID: 2195497
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  • 4. Ultrastructural findings in epidermolysis bullosa.
    Smith LT.
    Arch Dermatol; 1993 Dec; 129(12):1578-84. PubMed ID: 7504435
    [Abstract] [Full Text] [Related]

  • 5. [The dermo-epidermal junction and its acquired and hereditary pathology. A few recent advances].
    Ortonne JP.
    Pathol Biol (Paris); 1992 Feb; 40(2):121-32. PubMed ID: 1608653
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  • 6. Ultrastructure and molecular pathogenesis of epidermolysis bullosa.
    Shinkuma S, McMillan JR, Shimizu H.
    Clin Dermatol; 2011 Feb; 29(4):412-9. PubMed ID: 21679868
    [Abstract] [Full Text] [Related]

  • 7. Immunofluorescence antigen mapping for hereditary epidermolysis bullosa.
    Rao R, Mellerio J, Bhogal BS, Groves R.
    Indian J Dermatol Venereol Leprol; 2012 Feb; 78(6):692-7. PubMed ID: 23075637
    [Abstract] [Full Text] [Related]

  • 8. A specific defect in glycosylation of epidermal cell membranes. Definition in skin from patients with epidermolysis bullosa simplex.
    Fine JD, Griffith RD.
    Arch Dermatol; 1985 Oct; 121(10):1292-6. PubMed ID: 2412497
    [Abstract] [Full Text] [Related]

  • 9. Hemidesmosomes show abnormal association with the keratin filament network in junctional forms of epidermolysis bullosa.
    McMillan JR, McGrath JA, Tidman MJ, Eady RA.
    J Invest Dermatol; 1998 Feb; 110(2):132-7. PubMed ID: 9457907
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  • 10. Structural and functional properties of the dermoepidermal junction in obligate heterozygotes for recessive forms of epidermolysis bullosa.
    Tidman MJ, Eady RA.
    Arch Dermatol; 1986 Mar; 122(3):278-81. PubMed ID: 3954393
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  • 13. Monoclonal antibody GB3 defines a widespread defect of several basement membranes and a keratinocyte dysfunction in patients with lethal junctional epidermolysis bullosa.
    Verrando P, Blanchet-Bardon C, Pisani A, Thomas L, Cambazard F, Eady RA, Schofield O, Ortonne JP.
    Lab Invest; 1991 Jan; 64(1):85-92. PubMed ID: 1990210
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  • 16. Epidermolysis bullosa in Finland. Clinical features, morphology and relation to collagen metabolism.
    Kero M.
    Acta Derm Venereol Suppl (Stockh); 1984 Jan; 110():1-51. PubMed ID: 6331034
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  • 18. [Antenatal diagnosis of hereditary epidermolysis bullosa].
    Blanchet-Bardon C, Dumez Y, Nazzaro V, Mimoz C, Puissant A.
    Ann Dermatol Venereol; 1987 Jan; 114(4):525-39. PubMed ID: 3619299
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  • 20. Genetic abnormalities and clinical classification of epidermolysis bullosa.
    Mitsuhashi Y, Hashimoto I.
    Arch Dermatol Res; 2003 Apr; 295 Suppl 1():S29-33. PubMed ID: 12677430
    [Abstract] [Full Text] [Related]

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