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3. Prenatal diagnosis of dominant and recessive dystrophic epidermolysis bullosa: application and limitations in the use of KF-1 and LH 7:2 monoclonal antibodies and immunofluorescence mapping technique. Fine JD; Eady RA; Levy ML; Hejtmancik JF; Courtney KB; Carpenter RJ; Holbrook KA; Hawkins HK J Invest Dermatol; 1988 Nov; 91(5):465-71. PubMed ID: 3049834 [TBL] [Abstract][Full Text] [Related]
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 [TBL] [Abstract][Full Text] [Related]
5. [Antenatal diagnosis of hereditary epidermolysis bullosa]. Blanchet-Bardon C; Dumez Y; Nazzaro V; Mimoz C; Puissant A Ann Dermatol Venereol; 1987; 114(4):525-39. PubMed ID: 3619299 [TBL] [Abstract][Full Text] [Related]
7. 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 [TBL] [Abstract][Full Text] [Related]
8. Laboratory tests for epidermolysis bullosa. Fine JD Dermatol Clin; 1994 Jan; 12(1):123-32. PubMed ID: 8143376 [TBL] [Abstract][Full Text] [Related]
9. 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 [TBL] [Abstract][Full Text] [Related]
10. Successful prenatal exclusion of an unspecified subtype of severe epidermolysis bullosa. Shimizu H; Horiguchi Y; Suzumori K; Watanabe I; Owaribe K; Nishikawa T Int J Dermatol; 1998 May; 37(5):364-9. PubMed ID: 9620484 [TBL] [Abstract][Full Text] [Related]
11. Identification of an epidermal basement membrane defect in recessive forms of dystrophic epidermolysis bullosa by LH 7:2 monoclonal antibody: use in diagnosis. Heagerty AH; Kennedy AR; Leigh IM; Purkis P; Eady RA Br J Dermatol; 1986 Aug; 115(2):125-31. PubMed ID: 3527251 [TBL] [Abstract][Full Text] [Related]
12. GB3 monoclonal antibody for the diagnosis of junctional epidermolysis bullosa: results of a multicenter study. Schofield OM; Fine JD; Verrando P; Heagerty AH; Ortonne JP; Eady RA J Am Acad Dermatol; 1990 Dec; 23(6 Pt 1):1078-83. PubMed ID: 2273105 [TBL] [Abstract][Full Text] [Related]
13. Diagnosis and prenatal diagnosis of epidermolysis bullosa herpetiformis (Dowling-Meara) in a mother, two affected children, and an affected fetus. Holbrook KA; Wapner R; Jackson L; Zaeri N Prenat Diagn; 1992 Sep; 12(9):725-39. PubMed ID: 1438067 [TBL] [Abstract][Full Text] [Related]
14. Analysis of skin-derived amniotic fluid cells in the second trimester; detection of severe genodermatoses expressed in the fetal period. Akiyama M; Holbrook KA J Invest Dermatol; 1994 Nov; 103(5):674-7. PubMed ID: 7963655 [TBL] [Abstract][Full Text] [Related]
15. Epidermolysis bullosa simplex superficialis. A new variant of epidermolysis bullosa characterized by subcorneal skin cleavage mimicking peeling skin syndrome. Fine JD; Johnson L; Wright T Arch Dermatol; 1989 May; 125(5):633-8. PubMed ID: 2653224 [TBL] [Abstract][Full Text] [Related]
19. 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 [TBL] [Abstract][Full Text] [Related]
20. Heterogeneous reactivity with LH7.2 and the first prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa among Japanese patients. Shimizu H; Suzumori K; Nishikawa T Dermatology; 1996; 192(3):203-7. PubMed ID: 8726631 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]