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Results: 1 to 20 of 44

Related Articles by Review for PubMed (Select 16175511)

1.

Loss of desmoplakin tail causes lethal acantholytic epidermolysis bullosa.

Jonkman MF, Pasmooij AM, Pasmans SG, van den Berg MP, Ter Horst HJ, Timmer A, Pas HH.

Am J Hum Genet. 2005 Oct;77(4):653-60. Epub 2005 Aug 17.

2.

Lethal acantholytic epidermolysis bullosa.

McGrath JA, Bolling MC, Jonkman MF.

Dermatol Clin. 2010 Jan;28(1):131-5. doi: 10.1016/j.det.2009.10.015. Review.

PMID:
19945626
4.

Molecular abnormalities of the desmosomal protein desmoplakin in human disease.

Lai Cheong JE, Wessagowit V, McGrath JA.

Clin Exp Dermatol. 2005 May;30(3):261-6. Review.

PMID:
15807686
5.

Desmosomal genodermatoses.

Petrof G, Mellerio JE, McGrath JA.

Br J Dermatol. 2012 Jan;166(1):36-45. doi: 10.1111/j.1365-2133.2011.10640.x. Review.

PMID:
21929534
6.

Differential expression of pyloric atresia in junctional epidermolysis bullosa with ITGB4 mutations suggests that pyloric atresia is due to factors other than the mutations and not predictive of a poor outcome: three novel mutations and a review of the literature.

Dang N, Klingberg S, Rubin AI, Edwards M, Borelli S, Relic J, Marr P, Tran K, Turner A, Smith N, Murrell DF.

Acta Derm Venereol. 2008;88(5):438-48. doi: 10.2340/00015555-0484. Review.

7.

Ectodermal dysplasia-skin fragility syndrome.

McGrath JA, Mellerio JE.

Dermatol Clin. 2010 Jan;28(1):125-9. doi: 10.1016/j.det.2009.10.014. Review.

PMID:
19945625
8.

Dermatoses affecting desmosomes in animals: a mechanistic review of acantholytic blistering skin diseases.

Olivry T, Linder KE.

Vet Dermatol. 2009 Oct;20(5-6):313-26. doi: 10.1111/j.1365-3164.2009.00821.x. Review.

PMID:
20178467
9.

Clinical heterogeneity in recessive epidermolysis bullosa due to mutations in the keratin 14 gene, KRT14.

Yiasemides E, Trisnowati N, Su J, Dang N, Klingberg S, Marr P, Melbourne W, Tran K, Chow CW, Orchard D, Varigos G, Murrell DF.

Clin Exp Dermatol. 2008 Nov;33(6):689-97. doi: 10.1111/j.1365-2230.2008.02858.x. Epub 2008 Aug 16. Review.

PMID:
18713255
10.

[From gene to disease; epidermolysis bullosa due to mutations in proteins in or around the hemidesmosome].

Jonkman MF, Rulo HF, Duipmans JC.

Ned Tijdschr Geneeskd. 2003 Jun 7;147(23):1108-13. Review. Dutch.

PMID:
12822520
11.

Type XVII collagen gene mutations in junctional epidermolysis bullosa and prospects for gene therapy.

Bauer JW, Lanschuetzer C.

Clin Exp Dermatol. 2003 Jan;28(1):53-60. Review.

PMID:
12558632
12.

Desmosomes: structure and function in normal and diseased epidermis.

McMillan JR, Shimizu H.

J Dermatol. 2001 Jun;28(6):291-8. Review.

PMID:
11476106
14.

Human hair abnormalities resulting from inherited desmosome gene mutations.

McGrath JA, Wessagowit V.

Keio J Med. 2005 Jun;54(2):72-9. Review.

15.

In vivo function of desmosomes.

Cheng X, Koch PJ.

J Dermatol. 2004 Mar;31(3):171-87. Review.

PMID:
15187337
16.

Genetic disorders of palm skin and nail.

McLean WH; Epithelial Genetics Group.

J Anat. 2003 Jan;202(1):133-41. Review.

17.
18.

Insights into desmosome biology from inherited human skin disease and cardiocutaneous syndromes.

Nitoiu D, Etheridge SL, Kelsell DP.

Cell Commun Adhes. 2014 Jun;21(3):129-40. doi: 10.3109/15419061.2014.908854. Epub 2014 Apr 16. Review.

PMID:
24738885
19.

[Desmosomes and acantholytic diseases].

Machet MC, Arbeille B, Vaillant L.

Ann Dermatol Venereol. 1994;121(8):581-93. Review. French. No abstract available.

PMID:
7755319
20.

Progress in epidermolysis bullosa: from eponyms to molecular genetic classification.

Uitto J, Richard G.

Clin Dermatol. 2005 Jan-Feb;23(1):33-40. Review.

PMID:
15708287
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