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Results: 14

Related Articles by Review for PubMed (Select 7861014)

1.

A glycine-to-arginine substitution in the triple-helical domain of type VII collagen in a family with dominant dystrophic epidermolysis bullosa.

Christiano AM, Morricone A, Paradisi M, Angelo C, Mazzanti C, Cavalieri R, Uitto J.

J Invest Dermatol. 1995 Mar;104(3):438-40.

PMID:
7861014
2.

Review of collagen VII sequence variants found in Australasian patients with dystrophic epidermolysis bullosa reveals nine novel COL7A1 variants.

Dang N, Klingberg S, Marr P, Murrell DF.

J Dermatol Sci. 2007 Jun;46(3):169-78. Epub 2007 Apr 10. Review.

PMID:
17425959
3.

Mutation analysis and characterization of COL7A1 mutations in dystrophic epidermolysis bullosa.

Dang N, Murrell DF.

Exp Dermatol. 2008 Jul;17(7):553-68. doi: 10.1111/j.1600-0625.2008.00723.x. Review.

PMID:
18558993
4.

Molecular biology and pathology of type VII collagen.

Uitto J, Chung-Honet LC, Christiano AM.

Exp Dermatol. 1992 Jul;1(1):2-11. Review.

PMID:
1344657
5.

Clinical and molecular dilemmas in the diagnosis of familial epidermolysis bullosa pruriginosa.

Ee HL, Liu L, Goh CL, McGrath JA.

J Am Acad Dermatol. 2007 May;56(5 Suppl):S77-81. Review.

PMID:
17434045
6.
7.

Dystrophic forms of epidermolysis bullosa.

Uitto J, Christiano AM.

Semin Dermatol. 1993 Sep;12(3):191-201. Review.

PMID:
8217558
8.

Biology of anchoring fibrils: lessons from dystrophic epidermolysis bullosa.

Bruckner-Tuderman L, Höpfner B, Hammami-Hauasli N.

Matrix Biol. 1999 Feb;18(1):43-54. Review.

PMID:
10367730
9.

X-linked ichthyosis along with recessive dystrophic epidermolysis bullosa in the same patient.

Hernández-Martín A, Cuadrado-Corrales N, Ciria-Abad S, Arias-Palomo D, Mascaró-Galy JM, Escámez MJ, García M, Del Río M, Torrelo A, González-Sarmiento R.

Dermatology. 2010;221(2):113-6. doi: 10.1159/000313507. Epub 2010 Jun 4. Review.

PMID:
20523032
10.

Molecular basis for the dystrophic forms of epidermolysis bullosa: mutations in the type VII collagen gene.

Uitto J, Christiano AM.

Arch Dermatol Res. 1994;287(1):16-22. Review.

PMID:
7726631
11.

Pathogenesis of mechanobullous disorders.

Bruckner-Tuderman L.

Exp Dermatol. 1992 Oct;1(3):115-20. Review.

PMID:
1365310
12.

Epidermolysis bullosa: hereditary skin fragility diseases as paradigms in cell biology.

Eady RA, Dunnill MG.

Arch Dermatol Res. 1994;287(1):2-9. Review.

PMID:
7537032
13.

A novel de novo splice-site mutation in the COL7A1 gene in dominant dystrophic epidermolysis bullosa (DDEB): specific exon skipping could be a prognostic factor for DDEB pruriginosa.

Saito M, Masunaga T, Ishiko A.

Clin Exp Dermatol. 2009 Dec;34(8):e934-6. doi: 10.1111/j.1365-2230.2009.03254.x. Epub 2009 May 26. Review.

PMID:
19486058
14.

Advances in understanding and treating dystrophic epidermolysis bullosa.

Vanden Oever MJ, Tolar J.

F1000Prime Rep. 2014 May 6;6:35. doi: 10.12703/P6-35. eCollection 2014. Review.

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