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3. Genetic abnormalities and clinical classification of epidermolysis bullosa. Mitsuhashi Y; Hashimoto I Arch Dermatol Res; 2003 Apr; 295 Suppl 1():S29-33. PubMed ID: 12677430 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa. Shimizu H; Sato M; Ban M; Kitajima Y; Ishizaki S; Harada T; Bruckner-Tuderman L; Fine JD; Burgeson R; Kon A; McGrath JA; Christiano AM; Uitto J; Nishikawa T Arch Dermatol; 1997 Sep; 133(9):1111-7. PubMed ID: 9301588 [TBL] [Abstract][Full Text] [Related]
6. [Epidermolysis bullosa]. García Pérez A An R Acad Nac Med (Madr); 1999; 116(2):387-413; discussion 413-5. PubMed ID: 10682398 [TBL] [Abstract][Full Text] [Related]
12. [Hereditary epidermolysis bullosa: towards classification and genetic counseling based upon identification of molecular defects]. Hovnanian A; de Prost Y Arch Pediatr; 1994 Nov; 1(11):1028-33. PubMed ID: 7530560 [TBL] [Abstract][Full Text] [Related]
13. 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. Fine JD Arch Dermatol; 1990 Sep; 126(9):1187-90. PubMed ID: 2396835 [TBL] [Abstract][Full Text] [Related]
15. Epidermolysis bullosa in animals: a review. Medeiros GX; Riet-Correa F Vet Dermatol; 2015 Feb; 26(1):3-13, e1-2. PubMed ID: 25354580 [TBL] [Abstract][Full Text] [Related]
16. Epidermolysis bullosa simplex (Koebner) is a keratin disorder. Ultrastructural and immunohistochemical study. Ito M; Okuda C; Shimizu N; Tazawa T; Sato Y Arch Dermatol; 1991 Mar; 127(3):367-72. PubMed ID: 1705413 [TBL] [Abstract][Full Text] [Related]
17. 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; 122(3):278-81. PubMed ID: 3954393 [TBL] [Abstract][Full Text] [Related]
18. [The dermo-epidermal junction and its acquired and hereditary pathology. A few recent advances]. Ortonne JP Pathol Biol (Paris); 1992 Feb; 40(2):121-32. PubMed ID: 1608653 [TBL] [Abstract][Full Text] [Related]
19. Hemidesmosomal variants of epidermolysis bullosa. Mutations in the alpha6beta4 integrin and the 180-kD bullous pemphigoid antigen/type XVII collagen genes. Pulkkinen L; Uitto J Exp Dermatol; 1998; 7(2-3):46-64. PubMed ID: 9583744 [TBL] [Abstract][Full Text] [Related]
20. Ultrastructural clues to genetic disorders of skin: the dermal-epidermal junction. Eady RA; McGrath JA; McMillan JR J Invest Dermatol; 1994 Nov; 103(5 Suppl):13S-18S. PubMed ID: 7963675 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]