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Epidermolysis bullosa: review and report of caseCAROLL, D. L; STEPHAN, M. J; HAYS, G. L et al.The Journal of the American Dental Association (1939). 1983, Vol 107, Num 5, pp 749-751, issn 0002-8177Article

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

LES EPIDERMOLYSES BULLEUSES CONGENITALES.BARRIERE H; BOUBEIX Y; CABILLIC P et al.1978; OUEST MED.; FR.; DA. 1978; VOL. 31; NO 5; PP. 279-285Article

Expression of integrins in junctional and dystrophic epidermolysis bullosaNAZZARO, V; BERTI, E; CERRI, A et al.Journal of investigative dermatology. 1990, Vol 95, Num 1, pp 60-64, issn 0022-202XArticle

Occurrence of epidermolysis bullosa in FinlandKERO, M.Acta dermato-venereologica. 1984, Vol 64, Num 1, pp 57-62, issn 0001-5555Article

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

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

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 naevi reveal a distinctive dermoscopic patternLANSCHUETZER, C. M; EMBERGER, M; LAIMER, M et al.British journal of dermatology (1951). 2005, Vol 153, Num 1, pp 97-102, issn 0007-0963, 6 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

HEREDITAERE EPIDERMOLYSEN: KLASSIFIKATION, ERBPROGNOSE UND THERAPIE. = EPIDERMOLYSES HEREDITAIRES: CLASSIFICATION, PRONOSTIC GENETIQUE ET TRAITEMENTSCHNYDER UW.1976; FORTSCHR. PRAKT. DERMATOL. VENEROL.; DTSCH.; DA. 1976; VOL. 8; PP. 1-8; BIBL. 14 REF.Article

Sustainable correction of junctional epidermolysis bullosa via transposon-mediated nonviral gene transferORTIZ-URDA, S; LIN, Q; YANT, S. R et al.Gene therapy (Basingstoke). 2003, Vol 10, Num 13, pp 1099-1104, issn 0969-7128, 6 p.Article

Proteases are responsible for blister formation in recessive dystrophic epidermolysis bullosa and epidermolysis bullosa simplexTAKAMORI, K; IKEDA, S; NAITO, K et al.British journal of dermatology (1951). 1985, Vol 112, Num 5, pp 533-538, issn 0007-0963Article

ZUR WIRKSAMKEIT DES PHENYTOINS BEI DER BEHANDLUNG DER EPIDERMOLYSIS BULLOSA HEREDITARIA DYSTROPHICA PARTIM INVERSA (GEDDE-DAHL) = L'EFFICACITE DE LA PHENYTOINE DANS LE TRAITEMENT DE L'EPIDERMOLYSE BULLEUSE HEREDITAIRE DYSTROPHIQUE INVERSEE (GEDDE-DAHL)BANDMANN HJ; PERWEIN E.1982; H+G. ZEITSCHRIFT FUER HAUTKRANKHEITEN; ISSN 0301-0481; DEU; DA. 1982; VOL. 57; NO 21; PP. 1587-1598; 10 P.; ABS. ENG; BIBL. 2 P.Article

CARCINOEMBRYONIC ANTIGEN: INCREASED PLASMA LEVELS IN RECESSIVE EPIDERMOLYSIS BULLOSAROCHMAN H; COOPER M; ESTERLY NB et al.1979; J. INVEST. DERMATOL.; USA; DA. 1979; VOL. 72; NO 5; PP. 262-263; BIBL. 16 REF.Article

The Cockayne-Touraine type of dominant dystrophic epidermolysis bullosa―ultrastructural similarities to the Pasini variantOAKLEY, C. A; GAWKRODGER, D. J; ROSS, J. A et al.Acta dermato-venereologica. 1984, Vol 64, Num 3, pp 253-256, issn 0001-5555Article

ULTRASTRUCTURAL STUDIES IN EPIDERMOLYSIS BULLOSA HEREDITARIA. IV. RECESSIVE DYSTROPHIC TYPES WITH JUNCTIONAL BLISTERING. (INFANTILE OR HERLITZ-PEARSON TYPE AND ADULT TYPE).HASHIMOTO I; GEDDE DAHL T JR; SCHNYDER UW et al.1976; ARCH. DERMATOL. RES.; GERM.; DA. 1976; VOL. 257; NO 1; PP. 17-32; ABS. ALLEM.; BIBL. 25 REF.Article

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

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

Epidermolyse bulleuse jonctionnelle non létale: généralisée, atrophique et «bénigne» = Generalized atrophic benign epidermolysis bullosaPRIGENT, F; BLANCHET-BARDON, C; MARIANO, A et al.Annales de dermatologie et de vénéréologie. 1989, Vol 116, Num 11, pp 786-788, issn 0151-9638, 3 p.Conference Paper