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Journal Abstract Search

151 related items for PubMed ID: 2195497

  • 1. 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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  • 2. 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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  • 3. 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
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  • 4. Prenatal diagnosis of junctional epidermolysis bullosa associated with pyloric atresia.
    Nazzaro V, Nicolini U, De Luca L, Berti E, Caputo R.
    J Med Genet; 1990 Apr; 27(4):244-8. PubMed ID: 2182874
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  • 5. Ultrastructure and molecular pathogenesis of epidermolysis bullosa.
    Shinkuma S, McMillan JR, Shimizu H.
    Clin Dermatol; 2011 Apr; 29(4):412-9. PubMed ID: 21679868
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  • 8. Abnormal binding of an anti-amnion antibody to epidermal basement membrane provides a novel diagnostic probe for junctional epidermolysis bullosa.
    Kennedy AR, Heagerty AH, Ortonne JP, Hsi BL, Yeh CJ, Eady RA.
    Br J Dermatol; 1985 Dec; 113(6):651-9. PubMed ID: 3913455
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  • 9. Prenatal exclusion of Herlitz syndrome by electron microscopy of fetal skin biopsies obtained at fetoscopy.
    Löfberg L, Anton-Lamprecht I, Michaëlsson G, Gustavii B.
    Acta Derm Venereol; 1983 Dec; 63(3):185-9. PubMed ID: 6192629
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  • 10. LDA-1 monoclonal antibody. An excellent reagent for immunofluorescence mapping studies in patients with epidermolysis bullosa.
    Fine JD, Gay S.
    Arch Dermatol; 1986 Jan; 122(1):48-51. PubMed ID: 3510588
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  • 11. Rapid prenatal diagnosis of epidermolysis bullosa letalis using GB3 monoclonal antibody.
    Heagerty AH, Eady RA, Kennedy AR, Nicolaides KH, Rodeck CH, Hsi BL, Ortonne JP.
    Br J Dermatol; 1987 Sep; 117(3):271-5. PubMed ID: 3314965
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  • 12. 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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  • 15. Ultrastructural findings in epidermolysis bullosa.
    Smith LT.
    Arch Dermatol; 1993 Dec; 129(12):1578-84. PubMed ID: 7504435
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  • 16. [Antenatal diagnosis of hereditary epidermolysis bullosa].
    Blanchet-Bardon C, Dumez Y, Nazzaro V, Mimoz C, Puissant A.
    Ann Dermatol Venereol; 1987 Dec; 114(4):525-39. PubMed ID: 3619299
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  • 17. Immunofluorescence mapping of antigenic determinants within the dermal-epidermal junction in the mechanobullous diseases.
    Hintner H, Stingl G, Schuler G, Fritsch P, Stanley J, Katz S, Wolff K.
    J Invest Dermatol; 1981 Feb; 76(2):113-8. PubMed ID: 6161971
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  • 18. Prenatal diagnosis of genodermatoses by ultrastructural diagnostic markers in extra-embryonic tissues: defective hemidesmosomes in amnion epithelium of fetuses affected with epidermolysis bullosa Herlitz type (an alternative prenatal diagnosis in certain cases).
    Hausser I, Anton-Lamprecht I.
    Hum Genet; 1990 Aug; 85(3):367-75. PubMed ID: 2394450
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  • 19. Antigenic expression of integrin alpha 6 beta 4 in junctional epidermolysis bullosa.
    Phillips RJ, Aplin JD, Lake BD.
    Histopathology; 1994 Jun; 24(6):571-6. PubMed ID: 8063286
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  • 20. Ultrastructural studies in epidermolysis bullosa hereditaria. IV. Recessive dystrophic types with junctional blistering. (Infantile or Herlitz-Pearson type and adult type).
    Hashimoto I, Gedde-Dahl T, Schnyder UW, Anton-Lamprecht I.
    Arch Dermatol Res (1975); 1976 Nov 26; 257(1):17-32. PubMed ID: 1008602
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