222 related articles for article (PubMed ID: 1365310)
1. Pathogenesis of mechanobullous disorders.
Bruckner-Tuderman L
Exp Dermatol; 1992 Oct; 1(3):115-20. PubMed ID: 1365310
[TBL] [Abstract][Full Text] [Related]
2. Ultrastructural findings in epidermolysis bullosa.
Smith LT
Arch Dermatol; 1993 Dec; 129(12):1578-84. PubMed ID: 7504435
[TBL] [Abstract][Full Text] [Related]
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. Epidermolysis bullosa: pathophysiology and nursing care.
Gannon BA
Neonatal Netw; 2004; 23(6):25-32. PubMed ID: 15612418
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Using immunofluorescence (antigen) mapping in the diagnosis and classification of epidermolysis bullosa: a first report from Iran.
Barzegar M; Asadi-Kani Z; Mozafari N; Vahidnezhad H; Kariminejad A; Toossi P
Int J Dermatol; 2015 Oct; 54(10):e416-23. PubMed ID: 26220012
[TBL] [Abstract][Full Text] [Related]
7. Progress in epidermolysis bullosa: from eponyms to molecular genetic classification.
Uitto J; Richard G
Clin Dermatol; 2005; 23(1):33-40. PubMed ID: 15708287
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Mutation analysis and molecular genetics of epidermolysis bullosa.
Pulkkinen L; Uitto J
Matrix Biol; 1999 Feb; 18(1):29-42. PubMed ID: 10367729
[TBL] [Abstract][Full Text] [Related]
10. Structural variations in anchoring fibrils in dystrophic epidermolysis bullosa: correlation with type VII collagen expression.
McGrath JA; Ishida-Yamamoto A; O'Grady A; Leigh IM; Eady RA
J Invest Dermatol; 1993 Apr; 100(4):366-72. PubMed ID: 8454899
[TBL] [Abstract][Full Text] [Related]
11. The molecular basis for inherited bullous diseases.
Korge BP; Krieg T
J Mol Med (Berl); 1996 Feb; 74(2):59-70. PubMed ID: 8820401
[TBL] [Abstract][Full Text] [Related]
12. [Syndromes 13. Epidermolysis bullosa].
Meijndert L; Jonkman MF
Ned Tijdschr Tandheelkd; 1999 Aug; 106(8):302-5. PubMed ID: 11930425
[TBL] [Abstract][Full Text] [Related]
13. Epidermolysis bullosa: pathogenetic pathways from mutations to symptoms.
Bruckner-Tuderman L
Ann Med; 1994 Jun; 26(3):165-71. PubMed ID: 7521174
[TBL] [Abstract][Full Text] [Related]
14. Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-sense or frameshift mutations.
McGrath JA; Ashton GH; Mellerio JE; Salas-Alanis JC; Swensson O; McMillan JR; Eady RA
J Invest Dermatol; 1999 Sep; 113(3):314-21. PubMed ID: 10469327
[TBL] [Abstract][Full Text] [Related]
15. Bone mineralization in children with epidermolysis bullosa.
Fewtrell MS; Allgrove J; Gordon I; Brain C; Atherton D; Harper J; Mellerio JE; Martinez AE
Br J Dermatol; 2006 May; 154(5):959-62. PubMed ID: 16634901
[TBL] [Abstract][Full Text] [Related]
16. Molecular basis of the dystrophic and junctional forms of epidermolysis bullosa: mutations in the type VII collagen and kalinin (laminin 5) genes.
Uitto J; Pulkkinen L; Christiano AM
J Invest Dermatol; 1994 Nov; 103(5 Suppl):39S-46S. PubMed ID: 7963683
[TBL] [Abstract][Full Text] [Related]
17. Type VII collagen, anchoring fibrils, and epidermolysis bullosa.
Burgeson RE
J Invest Dermatol; 1993 Sep; 101(3):252-5. PubMed ID: 8370960
[TBL] [Abstract][Full Text] [Related]
18. Clinicopathological correlations of compound heterozygous COL7A1 mutations in recessive dystrophic epidermolysis bullosa.
Dunnill MG; McGrath JA; Richards AJ; Christiano AM; Uitto J; Pope FM; Eady RA
J Invest Dermatol; 1996 Aug; 107(2):171-7. PubMed ID: 8757758
[TBL] [Abstract][Full Text] [Related]
19. Instrument for scoring clinical outcome of research for epidermolysis bullosa: a consensus-generated clinical research tool.
Schwieger-Briel A; Chakkittakandiyil A; Lara-Corrales I; Aujla N; Lane AT; Lucky AW; Bruckner AL; Pope E
Pediatr Dermatol; 2015; 32(1):41-52. PubMed ID: 24650374
[TBL] [Abstract][Full Text] [Related]
20. Epidermolysis bullosa: hereditary skin fragility diseases as paradigms in cell biology.
Eady RA; Dunnill MG
Arch Dermatol Res; 1994; 287(1):2-9. PubMed ID: 7537032
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
