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Journal Abstract Search

151 related items for PubMed ID: 3204167

  • 1. Ultrastructure of junctional epidermolysis bullosa in Belgian foals.
    Johnson GC, Kohn CW, Johnson CW, Garry F, Scott D, Martin S.
    J Comp Pathol; 1988 Oct; 99(3):329-36. PubMed ID: 3204167
    [Abstract] [Full Text] [Related]

  • 2. Hereditary junctional mechanobullous disease in a foal.
    Frame SR, Harrington DD, Fessler J, Frame PF.
    J Am Vet Med Assoc; 1988 Dec 01; 193(11):1420-4. PubMed ID: 3209456
    [Abstract] [Full Text] [Related]

  • 3. Equine epitheliogenesis imperfecta in two american saddlebred foals is a lamina lucida defect.
    Lieto LD, Swerczek TW, Cothran EG.
    Vet Pathol; 2002 Sep 01; 39(5):576-80. PubMed ID: 12243468
    [Abstract] [Full Text] [Related]

  • 4. Ultrastructural findings in epidermolysis bullosa.
    Smith LT.
    Arch Dermatol; 1993 Dec 01; 129(12):1578-84. PubMed ID: 7504435
    [Abstract] [Full Text] [Related]

  • 5. Rudimentary hemidesmosome formation in congenital generalized junctional epidermolysis bullosa in the Sprague-Dawley rat.
    Brenneman KA, Olivry T, Dorman DC.
    Vet Pathol; 2000 Jul 01; 37(4):336-9. PubMed ID: 10896395
    [Abstract] [Full Text] [Related]

  • 6. Ultrastructure and molecular pathogenesis of epidermolysis bullosa.
    Shinkuma S, McMillan JR, Shimizu H.
    Clin Dermatol; 2011 Jul 01; 29(4):412-9. PubMed ID: 21679868
    [Abstract] [Full Text] [Related]

  • 7. Evidence for a functional defect of the lamina lucida in recessive dystrophic epidermolysis bullosa demonstrated by suction blisters.
    Tidman MJ, Eady RA.
    Br J Dermatol; 1984 Oct 01; 111(4):379-87. PubMed ID: 6487542
    [Abstract] [Full Text] [Related]

  • 8. Generalized atrophic benign form of junctional epidermolysis bullosa.
    Foldes C, Wallach D, Aubinière E, Vignon-Pennamen MD, Cottenot F.
    Dermatologica; 1988 Oct 01; 176(2):83-90. PubMed ID: 2453379
    [Abstract] [Full Text] [Related]

  • 9. 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
    [Abstract] [Full Text] [Related]

  • 10. Mechanobullous disease in two Belgian foals.
    Kohn CW, Johnson GC, Garry F, Johnson CW, Martin S, Scott DW.
    Equine Vet J; 1989 Jul 26; 21(4):297-301. PubMed ID: 2767032
    [No Abstract] [Full Text] [Related]

  • 11. First report of junctional epidermolysis bullosa (JEB) in the Italian draft horse.
    Cappelli K, Brachelente C, Passamonti F, Flati A, Silvestrelli M, Capomaccio S.
    BMC Vet Res; 2015 Mar 10; 11():55. PubMed ID: 25889423
    [Abstract] [Full Text] [Related]

  • 12. A disease resembling junctional epidermolysis bullosa in a toy poodle.
    Dunstan RW, Sills RC, Wilkinson JE, Paller AS, Hashimoto KH.
    Am J Dermatopathol; 1988 Oct 10; 10(5):442-7. PubMed ID: 3228192
    [Abstract] [Full Text] [Related]

  • 13. 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 10; 84(5):374-7. PubMed ID: 4039741
    [Abstract] [Full Text] [Related]

  • 14. 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 10; 54(1):109-18. PubMed ID: 16174790
    [Abstract] [Full Text] [Related]

  • 15. 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 10; 76(2):113-8. PubMed ID: 6161971
    [Abstract] [Full Text] [Related]

  • 16. [From gene to disease; epidermolysis bullosa due to mutations in proteins in or around the hemidesmosome].
    Jonkman MF, Rulo HF, Duipmans JC.
    Ned Tijdschr Geneeskd; 2003 Jun 07; 147(23):1108-13. PubMed ID: 12822520
    [Abstract] [Full Text] [Related]

  • 17.
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    [No Abstract] [Full Text] [Related]

  • 18. Epidermolysis bullosa simplex with mottled pigmentation.
    Bruckner-Tuderman L, Vogel A, Rüegger S, Odermatt B, Tönz O, Schnyder UW.
    J Am Acad Dermatol; 1989 Aug 07; 21(2 Pt 2):425-32. PubMed ID: 2474016
    [Abstract] [Full Text] [Related]

  • 19. Monoclonal antibody GB3, a new probe for the study of human basement membranes and hemidesmosomes.
    Verrando P, Hsi BL, Yeh CJ, Pisani A, Serieys N, Ortonne JP.
    Exp Cell Res; 1987 May 07; 170(1):116-28. PubMed ID: 2436931
    [Abstract] [Full Text] [Related]

  • 20. Epidermolysis bullosa hereditaria letalis: report of a case and probable ultrastructural defects.
    Hashimoto I, Anton-Lamprecht I, Meyburg P.
    Helv Paediatr Acta; 1976 Apr 07; 30(6):543-52. PubMed ID: 1270327
    [Abstract] [Full Text] [Related]

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