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29. Autosomal recessive epidermolysis bullosa simplex. Generalized phenotypic features suggestive of junctional or dystrophic epidermolysis bullosa, and association with neuromuscular diseases. Fine JD; Stenn J; Johnson L; Wright T; Bock HG; Horiguchi Y Arch Dermatol; 1989 Jul; 125(7):931-8. PubMed ID: 2662909 [TBL] [Abstract][Full Text] [Related]
33. 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]
36. [Pathomorphogenesis of blistering in epidermolysis bullosa acquisita and epidermolysis bullosa dystrophica (author's transl)]. Metz J; Frank H; Metz G Arch Dermatol Res (1975); 1975 Nov; 254(1):103-12. PubMed ID: 1239240 [TBL] [Abstract][Full Text] [Related]
37. Protease inhibitor therapy for recessive dystrophic epidermolysis bullosa. In vitro effect and clinical trial with camostat mesylate. Ikeda S; Manabe M; Muramatsu T; Takamori K; Ogawa H J Am Acad Dermatol; 1988 Jun; 18(6):1246-52. PubMed ID: 3385039 [TBL] [Abstract][Full Text] [Related]
38. The Cockayne-Touraine type of dominant dystrophic epidermolysis bullosa--ultrastructural similarities to the Pasini variant. Oakley CA; Gawkrodger DJ; Ross JA; Hunter JA Acta Derm Venereol; 1984; 64(3):253-6. PubMed ID: 6204490 [TBL] [Abstract][Full Text] [Related]
39. 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]