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Journal Abstract Search

246 related items for PubMed ID: 21679868

  • 1. Ultrastructure and molecular pathogenesis of epidermolysis bullosa.
    Shinkuma S, McMillan JR, Shimizu H.
    Clin Dermatol; 2011; 29(4):412-9. PubMed ID: 21679868
    [Abstract] [Full Text] [Related]

  • 2. Ultrastructural findings in epidermolysis bullosa.
    Smith LT.
    Arch Dermatol; 1993 Dec; 129(12):1578-84. PubMed ID: 7504435
    [Abstract] [Full Text] [Related]

  • 3. Colocalization of multiple laminin isoforms predominantly beneath hemidesmosomes in the upper lamina densa of the epidermal basement membrane.
    McMillan JR, Akiyama M, Nakamura H, Shimizu H.
    J Histochem Cytochem; 2006 Jan; 54(1):109-18. PubMed ID: 16174790
    [Abstract] [Full Text] [Related]

  • 4. Inherited epidermolysis bullosa: new diagnostic criteria and classification.
    Intong LR, Murrell DF.
    Clin Dermatol; 2012 Jan; 30(1):70-7. PubMed ID: 22137229
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  • 5. A comparative study between transmission electron microscopy and immunofluorescence mapping in the diagnosis of epidermolysis bullosa.
    Yiasemides E, Walton J, Marr P, Villanueva EV, Murrell DF.
    Am J Dermatopathol; 2006 Oct; 28(5):387-94. PubMed ID: 17012912
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  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9. Immunofluorescence antigen mapping for hereditary epidermolysis bullosa.
    Rao R, Mellerio J, Bhogal BS, Groves R.
    Indian J Dermatol Venereol Leprol; 2012 Apr; 78(6):692-7. PubMed ID: 23075637
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  • 11. [Immunofluorescence mapping for diagnosis of congenital epidermolysis bullosa].
    Cepeda-Valdés R, Pohla-Gubo G, Borbolla-Escoboza JR, Barboza-Quintana O, Ancer-Rodríguez J, Hintner H, Salas-Alanis JC.
    Actas Dermosifiliogr; 2010 Oct; 101(8):673-82. PubMed ID: 20965010
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  • 13. Overview of epidermolysis bullosa.
    Sawamura D, Nakano H, Matsuzaki Y.
    J Dermatol; 2010 Mar; 37(3):214-9. PubMed ID: 20507384
    [Abstract] [Full Text] [Related]

  • 14. 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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  • 15. Rudimentary hemidesmosome formation in congenital generalized junctional epidermolysis bullosa in the Sprague-Dawley rat.
    Brenneman KA, Olivry T, Dorman DC.
    Vet Pathol; 2000 Jul; 37(4):336-9. PubMed ID: 10896395
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  • 17. Diagnosing epidermolysis bullosa type and subtype in infancy using immunofluorescence microscopy: the Stanford experience.
    Berk DR, Jazayeri L, Marinkovich MP, Sundram UN, Bruckner AL.
    Pediatr Dermatol; 2013 Jul; 30(2):226-33. PubMed ID: 23461686
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  • 20. The molecular genetics of basement membrane diseases.
    Marinkovich MP.
    Arch Dermatol; 1993 Dec; 129(12):1557-65. PubMed ID: 8250577
    [Abstract] [Full Text] [Related]

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