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Journal Abstract Search

493 related items for PubMed ID: 10682398

  • 1. [Epidermolysis bullosa].
    García Pérez A.
    An R Acad Nac Med (Madr); 1999; 116(2):387-413; discussion 413-5. PubMed ID: 10682398
    [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. Progress in epidermolysis bullosa: genetic classification and clinical implications.
    Uitto J, Richard G.
    Am J Med Genet C Semin Med Genet; 2004 Nov 15; 131C(1):61-74. PubMed ID: 15468152
    [Abstract] [Full Text] [Related]

  • 4. The molecular genetics of basement membrane diseases.
    Marinkovich MP.
    Arch Dermatol; 1993 Dec 15; 129(12):1557-65. PubMed ID: 8250577
    [Abstract] [Full Text] [Related]

  • 5. Genetic abnormalities and clinical classification of epidermolysis bullosa.
    Mitsuhashi Y, Hashimoto I.
    Arch Dermatol Res; 2003 Apr 15; 295 Suppl 1():S29-33. PubMed ID: 12677430
    [Abstract] [Full Text] [Related]

  • 6. Inherited epidermolysis bullosa: new diagnostic criteria and classification.
    Intong LR, Murrell DF.
    Clin Dermatol; 2012 Apr 15; 30(1):70-7. PubMed ID: 22137229
    [Abstract] [Full Text] [Related]

  • 7. Study of elastase-type activity in blister fluids of recessive dystrophic epidermolysis bullosa.
    Francès C, Meimon G, Herson S, Robert L.
    Clin Physiol Biochem; 1986 Apr 15; 4(6):350-4. PubMed ID: 3643827
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  • 9. Do mutations in the basement membrane zone affect the human periodontium? Review with special reference to epidermolysis bullosa.
    Wiebe CB, Larjava HS.
    J West Soc Periodontol Periodontal Abstr; 1998 Apr 15; 46(1):5-18. PubMed ID: 9709672
    [Abstract] [Full Text] [Related]

  • 10. [Syndromes 13. Epidermolysis bullosa].
    Meijndert L, Jonkman MF.
    Ned Tijdschr Tandheelkd; 1999 Aug 15; 106(8):302-5. PubMed ID: 11930425
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  • 12. The molecular basis for inherited bullous diseases.
    Korge BP, Krieg T.
    J Mol Med (Berl); 1996 Feb 15; 74(2):59-70. PubMed ID: 8820401
    [Abstract] [Full Text] [Related]

  • 13. [Hereditary epidermolysis bullosa: towards classification and genetic counseling based upon identification of molecular defects].
    Hovnanian A, de Prost Y.
    Arch Pediatr; 1994 Nov 15; 1(11):1028-33. PubMed ID: 7530560
    [Abstract] [Full Text] [Related]

  • 14. Persistent subepidermal blistering in split-thickness skin graft sites. Ultrastructural and antigenic features simulating dystrophic or immunofluorescence-negative acquired epidermolysis bullosa.
    Epstein A, Hendrick SJ, Sanchez RL, Solomon AR, Fine JD.
    Arch Dermatol; 1988 Feb 15; 124(2):244-9. PubMed ID: 3277544
    [Abstract] [Full Text] [Related]

  • 15. Immunofluorescence antigen mapping for hereditary epidermolysis bullosa.
    Rao R, Mellerio J, Bhogal BS, Groves R.
    Indian J Dermatol Venereol Leprol; 2012 Feb 15; 78(6):692-7. PubMed ID: 23075637
    [Abstract] [Full Text] [Related]

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  • 18. 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 15; 122(3):278-81. PubMed ID: 3954393
    [Abstract] [Full Text] [Related]

  • 19. Mutation analysis and molecular genetics of epidermolysis bullosa.
    Pulkkinen L, Uitto J.
    Matrix Biol; 1999 Feb 15; 18(1):29-42. PubMed ID: 10367729
    [Abstract] [Full Text] [Related]

  • 20. Clinicopathologic types of epidermolysis bullosa and their nondermatological complications.
    Pearson RW.
    Arch Dermatol; 1988 May 15; 124(5):718-25. PubMed ID: 3284470
    [Abstract] [Full Text] [Related]

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