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9. Cicatricial junctional epidermolysis bullosa. Haber RM; Hanna W; Ramsay CA; Boxall LB J Am Acad Dermatol; 1985 May; 12(5 Pt 1):836-44. PubMed ID: 4008687 [TBL] [Abstract][Full Text] [Related]
10. Hemidesmosomes show abnormal association with the keratin filament network in junctional forms of epidermolysis bullosa. McMillan JR; McGrath JA; Tidman MJ; Eady RA J Invest Dermatol; 1998 Feb; 110(2):132-7. PubMed ID: 9457907 [TBL] [Abstract][Full Text] [Related]
11. 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 [TBL] [Abstract][Full Text] [Related]
12. Ultrastructural studies in epidermolysis bullosa heriditaria. I. Dominant dystrophic type of Pasini. Hashimoto I; Anton-Lamprecht I; Gedde-Dahl T; Schnyder UW Arch Dermatol Forsch; 1975; 252(3):167-78. PubMed ID: 1155959 [TBL] [Abstract][Full Text] [Related]
13. Generalized atrophic benign form of junctional epidermolysis bullosa. Foldes C; Wallach D; Aubinière E; Vignon-Pennamen MD; Cottenot F Dermatologica; 1988; 176(2):83-90. PubMed ID: 2453379 [TBL] [Abstract][Full Text] [Related]
14. Epidermolysis bullosa letalis (Herlitz disease): a case report. Singalavanija S; Phuvichit B; Palungwachira P J Med Assoc Thai; 1994 Feb; 77(2):103-7. PubMed ID: 7798834 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Epidermolysis bullosa hereditaria letalis: pathology, natural history and therapy. Schachner L; Lazarus GS; Dembitzer H Br J Dermatol; 1977 Jan; 96(1):51-8. PubMed ID: 843437 [TBL] [Abstract][Full Text] [Related]
17. [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]
18. Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations. McGrath JA; Ashton GH; Mellerio JE; Salas-Alanis JC; Swensson O; McMillan JR; Eady RA J Invest Dermatol; 1999 Sep; 113(3):314-21. PubMed ID: 10469327 [TBL] [Abstract][Full Text] [Related]
19. Ultrastructural studies in epidermolysis bullosa hereditaria. II. Dominant dystrophic type of Cockayne and Touraine. Hashimoto I; Gedde-Dahl T; Schnyder UW; Anton-Lamprecht I Arch Dermatol Res (1975); 1976 Jun; 255(3):285-95. PubMed ID: 942257 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]