Heavy and light chain isotypes of immunoglobulin in epidermolysis bullosa acquisitaMOONEY, E; GAMMON, W. R.Journal of investigative dermatology. 1990, Vol 95, Num 3, pp 317-319, issn 0022-202XArticle

Omiderm: a synthetic cover for exposed areas in epidermolysis bullosaAMIRAM SAGI; STAHL, N; HAUBEN, D et al.Annals of plastic surgery. 1988, Vol 20, Num 2, pp 133-135, issn 0148-7043Article

The mechanobullous diseasesTABAS, M; GIBBONS, S; BAUER, E. A et al.Dermatologic clinics. 1987, Vol 5, Num 1, pp 123-136, issn 0733-8635Article

Intra-epidermal retention of type VII collagen in a patient with recessive dystrophic epidermolysis bullosaSMITH, L. T; SYBERT, V. P.Journal of investigative dermatology. 1990, Vol 94, Num 2, pp 261-264, issn 0022-202XArticle

Recessive dystrophic epidermolysis bullosa skin displays a chronic growth-activated immunophenotype: implications for carcinogenesisSMOLLER, B. A; MCNUTT, N. S; CARTER, D. M et al.Archives of dermatology (1960). 1990, Vol 126, Num 1, pp 78-83, issn 0003-987X, 6 p.Article

Epidermólisis ampollosa mutilante de Hallopeau-Siemens. Estudio clínico, patológico, ultraestructural e inmunohistológico : sus actuales interrogantes = Epidermolysis bullosa type Hallopeau-Siemens. Report of two casesTORRES PERIS, V; JORDA CUEVAS, E; RAMON QUILIS, L et al.Actas dermo-sifiliográficas (Ed. impresa). 1990, Vol 81, Num 11, pp 791-797, issn 0001-7310, 7 p.Article

Human nidogen gene : identification of multiple RFLP and exclusion as candidate gene in a family with epidermolysis bullosa (EBS2) with evidence for linkage to chromosome 1HUMPHRIES, M; NAGAYOSHI, T; SHEILS, D et al.Journal of investigative dermatology. 1990, Vol 95, Num 5, pp 568-570, issn 0022-202XArticle

A bibliography of epidermolysis bullosaPRIESTLEY, G. C.Acta dermato-venereologica. Supplementum. 1987, Num 133, issn 0365-8341, 38 p.Serial Issue

Inherited epidermolysis bullosa in CroataFINE, J.-D; JOHNSON, L. B.Pediatric dermatology. 1990, Vol 7, Num 2, pp 147-149, issn 0736-8046, 3 p.Article

Epidermolysis bullosa : to split and to clumpEADY, R. A. J.Pediatric dermatology. 1992, Vol 9, Num 4, pp 361-364, issn 0736-8046Conference Paper

Epidermolysis bullosa acquisitaNAIR, L. V; GANGA, P.Indian Journal of Dermatology Venereology and Leprology. 1990, Vol 56, Num 4, pp 310-311, issn 0378-6323Article

Epidermolysis bullosa acquisita. Report of three casesKHATRI, M. L; SHAFI, M.Indian Journal of Dermatology Venereology and Leprology. 1989, Vol 55, Num 4, pp 244-247, issn 0378-6323, 4 p.Article

Epidermolysis bullosa: radiographic findings in 16 casesMAURO, M. A; PARKER, L. A; HARTLEY, W. S et al.American journal of roentgenology (1976). 1987, Vol 149, Num 5, pp 925-927, issn 0361-803XArticle

Epidermolysis bullosaLIN, A. N; CARTER, D. M.Annual review of medicine. 1993, Vol 44, pp 189-199, issn 0066-4219Article

Comprehensive dental care and general anesthetic management of hereditary epidermolysis bullosa : a review of fourteen casesTIM WRIGHT, J.Oral surgery, oral medicine, oral pathology. 1990, Vol 70, Num 5, pp 573-578, issn 0030-4220Article

X-Linked Ichthyosis along with Recessive Dystrophic Epidermolysis Bullosa in the Same PatientHERNANDEZ-MARTIN, A; CUADRADO-CORRALES, N; CIRIA-ABAD, S et al.Dermatology (Basel). 2010, Vol 221, Num 2, pp 113-116, issn 1018-8665, 4 p.Article

Structural and functional properties of the dermoepidermal junction in obligate heterozygotes for recessive forms of epidermolysis bullosaTIDMAN, M. J; EADY, R. A. J.Archives of dermatology (1960). 1986, Vol 122, Num 3, pp 278-281, issn 0003-987XArticle

Épidermolyse bulleuse dystrophique albupapuloïde de type Pasini : une pathologie exceptionnelle = Pasini typealbupapuloid dystrophicepjdermolysis bullosa : Asiexceptfonal diseaseRALANDISON, S; SAMISON, L. H; RAMAROZATOVO, L.-S et al.Les Nouvelles dermatologiques. 2007, Vol 26, Num 6, pp 400-403, issn 0752-5370, 4 p.Article

Epidermolysis bullosa hereditariaBRUCKNER-TUDERMAN, L.Hautarzt. 1995, Vol 46, Num 1, pp 61-72, issn 0017-8470Article

Mild recessive dystrophic epidermolysis bullosa associated with two compound heterozygous COL7A1 mutationsVON BARTENWERFFER, Wibke; HAS, Cristina; KRIEG, Thomas et al.EJD. European journal of dermatology. 2011, Vol 21, Num 2, pp 170-172, issn 1167-1122, 3 p.Article

Ultrasound-guided axillary plexus block in a child with dystrophic epidermolysis bullosaENGLBRECHT, J. S; LANGER, M; HAHNENKAMP, K et al.Anaesthesia and intensive care. 2010, Vol 38, Num 6, pp 1101-1105, issn 0310-057X, 5 p.Article

Epidermolysis bullosa : hereditary skin fragility diseases as paradigms in cell biologyEADY, R. A. J; DUNNILL, M. G. S.Archives of dermatological research (Print). 1994, Vol 287, Num 1, pp 2-9, issn 0340-3696Article

Glycosaminoglycans production by cultured skin fibroblasts from the Pasini and Cockayne-Touraine forms of dominant dystrophic epidermolysis bullosaPRIESTLEY, G. C.Journal of investigative dermatology. 1991, Vol 96, Num 2, pp 168-171, issn 0022-202XArticle

Séminaire de dermatologie pédiatrique (Paris, 14 mai 1993)de Prost, Yves; Amoric, J. C; Andry, P et al.Séminaire de dermatologie pédiatrique. 1993, 123 p.Conference Proceedings

Expression of the αβ4 integrin in lesional skin differentiates bullous pemphigoid (BP) from epidermolysis bullosa acquisita (EBA)MICHALAKI, H; STAQUET, M.-J; CERRI, A et al.Journal of investigative dermatology. 1992, Vol 98, Num 2, pp 204-208, issn 0022-202XArticle