Fine, Jo-David; Johnson, Lorraine B; Weiner, Madeline et al. (2007) Tracheolaryngeal complications of inherited epidermolysis bullosa: cumulative experience of the national epidermolysis bullosa registry. Laryngoscope 117:1652-60
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Chan, L S; Fine, J D; Hammerberg, C et al. (1995) Defective in vivo expression and apparently normal in vitro expression of a newly identified 105-kDa lower lamina lucida protein in dystrophic epidermolysis bullosa. Br J Dermatol 132:725-9
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Wright, J T; Johnson, L B; Fine, J D (1993) Development defects of enamel in humans with hereditary epidermolysis bullosa. Arch Oral Biol 38:945-55
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Chopra, V; Tyring, S K; Johnson, L et al. (1992) Peripheral blood mononuclear cell subsets in patients with severe inherited forms of epidermolysis bullosa. Arch Dermatol 128:201-9
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Fine, J D (1991) Structure and antigenicity of the skin basement membrane zone. J Cutan Pathol 18:401-9
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Fine, J D; Johnson, L B; Wright, J T (1991) Inherited blistering diseases of the skin. Pediatrician 18:175-87
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Wright, J T; Fine, J D; Johnson, L B (1991) Oral soft tissues in hereditary epidermolysis bullosa. Oral Surg Oral Med Oral Pathol 71:440-6
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Fine, J D; Bauer, E A; Briggaman, R A et al. (1991) Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry. J Am Acad Dermatol 24:119-35
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Fine, J D (1990) 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. Arch Dermatol 126:1187-90
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Fine, J D; Horiguchi, Y; Stein, D H et al. (1990) Intraepidermal type VII collagen. Evidence for abnormal intracytoplasmic processing of a major basement membrane protein in rare patients with dominant and possibly localized recessive forms of dystrophic epidermolysis bullosa. J Am Acad Dermatol 22:188-95
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