204 related articles for article (PubMed ID: 10218683)
1. Immunohistopathologic diagnosis of epidermolysis bullosa.
Bergman R
Am J Dermatopathol; 1999 Apr; 21(2):185-92. PubMed ID: 10218683
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Mosaic expression of uncein and 180-kDa bullous pemphigoid antigen in generalized atrophic benign epidermolysis bullosa.
Matsumura Y; Horiguchi Y; Toda K; Fujii H; Kore-Eda S; Tachibana T; Ohta K; Okamoto H; Imamura S
Br J Dermatol; 1997 May; 136(5):757-61. PubMed ID: 9205513
[TBL] [Abstract][Full Text] [Related]
4. Hemidesmosomal molecular changes in dermatitis herpetiformis; decreased expression of BP230 and plectin/HD1 in uninvolved skin.
Leivo T; Lohi J; Kariniemi AL; Molander G; Kiraly CL; Kotovirta ML; Owaribe K; Burgeson RE; Leivo I
Histochem J; 1999 Feb; 31(2):109-16. PubMed ID: 10416682
[TBL] [Abstract][Full Text] [Related]
5. The 97 kDa linear IgA bullous dermatosis antigen is not expressed in a patient with generalized atrophic benign epidermolysis bullosa with a novel homozygous G258X mutation in COL17A1.
Shimizu H; Takizawa Y; Pulkkinen L; Zone JJ; Matsumoto K; Saida T; Uitto J; Nishikawa T
J Invest Dermatol; 1998 Nov; 111(5):887-92. PubMed ID: 9804354
[TBL] [Abstract][Full Text] [Related]
6. Molecular complexity of the cutaneous basement membrane zone. Revelations from the paradigms of epidermolysis bullosa.
Christiano AM; Uitto J
Exp Dermatol; 1996 Feb; 5(1):1-11. PubMed ID: 8624605
[TBL] [Abstract][Full Text] [Related]
7. Ultrastructural findings in epidermolysis bullosa.
Smith LT
Arch Dermatol; 1993 Dec; 129(12):1578-84. PubMed ID: 7504435
[TBL] [Abstract][Full Text] [Related]
8. The role of immunohistochemistry in the diagnosis of the non-lethal forms of junctional epidermolysis bullosa.
McGrath JA; Eady RA
J Dermatol Sci; 1997 Jan; 14(1):68-75. PubMed ID: 9049810
[TBL] [Abstract][Full Text] [Related]
9. Prognostic implications of determining 180 kDa bullous pemphigoid antigen (BPAG2) gene/protein pathology in neonatal junctional epidermolysis bullosa.
Mellerio JE; Denyer JE; Atherton DJ; Eady RA; McGrath JA
Br J Dermatol; 1998 Apr; 138(4):661-6. PubMed ID: 9640376
[TBL] [Abstract][Full Text] [Related]
10. Lack of type VII collagen in unaffected skin of patients with severe recessive dystrophic epidermolysis bullosa.
Bruckner-Tuderman L; Rüegger S; Odermatt B; Mitsuhashi Y; Schnyder UW
Dermatologica; 1988; 176(2):57-64. PubMed ID: 3286309
[TBL] [Abstract][Full Text] [Related]
11. Junctional epidermolysis bullosa in the Middle East: clinical and genetic studies in a series of consanguineous families.
Nakano A; Lestringant GG; Paperna T; Bergman R; Gershoni R; Frossard P; Kanaan M; Meneguzzi G; Richard G; Pfendner E; Uitto J; Pulkkinen L; Sprecher E
J Am Acad Dermatol; 2002 Apr; 46(4):510-6. PubMed ID: 11907499
[TBL] [Abstract][Full Text] [Related]
12. 180-kD bullous pemphigoid antigen (BP180) is deficient in generalized atrophic benign epidermolysis bullosa.
Jonkman MF; de Jong MC; Heeres K; Pas HH; van der Meer JB; Owaribe K; Martinez de Velasco AM; Niessen CM; Sonnenberg A
J Clin Invest; 1995 Mar; 95(3):1345-52. PubMed ID: 7883981
[TBL] [Abstract][Full Text] [Related]
13. Prenatal exclusion of pyloric atresia-junctional epidermolysis bullosa syndrome.
Shimizu H; Fine JD; Suzumori K; Hatta N; Shozu M; Nishikawa T
J Am Acad Dermatol; 1994 Sep; 31(3 Pt 1):429-33. PubMed ID: 8077467
[TBL] [Abstract][Full Text] [Related]
14. Deletion of the cytoplasmatic domain of BP180/collagen XVII causes a phenotype with predominant features of epidermolysis bullosa simplex.
Huber M; Floeth M; Borradori L; Schäcke H; Rugg EL; Lane EB; Frenk E; Hohl D; Bruckner-Tuderman L
J Invest Dermatol; 2002 Jan; 118(1):185-92. PubMed ID: 11851893
[TBL] [Abstract][Full Text] [Related]
15. Digenic junctional epidermolysis bullosa: mutations in COL17A1 and LAMB3 genes.
Floeth M; Bruckner-Tuderman L
Am J Hum Genet; 1999 Dec; 65(6):1530-7. PubMed ID: 10577906
[TBL] [Abstract][Full Text] [Related]
16. Junctional epidermolysis bullosa with pyloric stenosis presenting with electron microscopic findings suggestive of epidermolysis bullosa simplex.
Wasel N; Idikio H; Lees G; Krol A; Lin AN
Pediatr Dermatol; 2000; 17(5):395-8. PubMed ID: 11085671
[TBL] [Abstract][Full Text] [Related]
17. Epidermolysis bullosa dystrophica inversa in a child.
Bruckner-Tuderman L; Pfaltz M; Schnyder UW
Pediatr Dermatol; 1990 Jun; 7(2):116-21. PubMed ID: 2193305
[TBL] [Abstract][Full Text] [Related]
18. Inherited epidermolysis bullosa: new diagnostic criteria and classification.
Intong LR; Murrell DF
Clin Dermatol; 2012; 30(1):70-7. PubMed ID: 22137229
[TBL] [Abstract][Full Text] [Related]
19. Defining target antigens in linear IgA disease using skin from subjects with inherited epidermolysis bullosa as a substrate for indirect immunofluorescence microscopy.
Harman KE; Bhogal BS; Eady RA; McGrath JA; Black MM
Br J Dermatol; 1999 Sep; 141(3):475-80. PubMed ID: 10583051
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
