McLean WH - Search Results

1

Mutations in keratin K9 in kindreds with epidermolytic palmoplantar keratoderma and epidemiology in Northern Ireland.

Covello SP, Irvine AD, McKenna KE, Munro CS, Nevin NC, Smith FJ, Uitto J, McLean WH. Covello SP, et al. Among authors: mclean wh. J Invest Dermatol. 1998 Dec;111(6):1207-9. doi: 10.1046/j.1523-1747.1998.00445.x. J Invest Dermatol. 1998. PMID: 9856842 Free article.

2

A novel connexin 30 mutation in Clouston syndrome.

Smith FJ, Morley SM, McLean WH. Smith FJ, et al. Among authors: mclean wh. J Invest Dermatol. 2002 Mar;118(3):530-2. doi: 10.1046/j.0022-202x.2001.01689.x. J Invest Dermatol. 2002. PMID: 11874494 Free article.

3

Frameshift mutation in the V2 domain of human keratin 1 results in striate palmoplantar keratoderma.

Whittock NV, Smith FJ, Wan H, Mallipeddi R, Griffiths WA, Dopping-Hepenstal P, Ashton GH, Eady RA, McLean WH, McGrath JA. Whittock NV, et al. Among authors: mclean wh. J Invest Dermatol. 2002 May;118(5):838-44. doi: 10.1046/j.1523-1747.2002.01750.x. J Invest Dermatol. 2002. PMID: 11982762 Free article.

4

Two cases of primarily palmoplantar keratoderma associated with novel mutations in keratin 1.

Terron-Kwiatkowski A, Paller AS, Compton J, Atherton DJ, McLean WH, Irvine AD. Terron-Kwiatkowski A, et al. Among authors: mclean wh. J Invest Dermatol. 2002 Oct;119(4):966-71. doi: 10.1046/j.1523-1747.2002.00186.x. J Invest Dermatol. 2002. PMID: 12406346 Free article.

5

Novel mechanism of revertant mosaicism in Dowling-Meara epidermolysis bullosa simplex.

Smith FJ, Morley SM, McLean WH. Smith FJ, et al. Among authors: mclean wh. J Invest Dermatol. 2004 Jan;122(1):73-7. doi: 10.1046/j.0022-202X.2003.22129.x. J Invest Dermatol. 2004. PMID: 14962092 Free article.

6

The genetic basis of pachyonychia congenita.

Smith FJ, Liao H, Cassidy AJ, Stewart A, Hamill KJ, Wood P, Joval I, van Steensel MA, Björck E, Callif-Daley F, Pals G, Collins P, Leachman SA, Munro CS, McLean WH. Smith FJ, et al. Among authors: mclean wh. J Investig Dermatol Symp Proc. 2005 Oct;10(1):21-30. doi: 10.1111/j.1087-0024.2005.10204.x. J Investig Dermatol Symp Proc. 2005. PMID: 16250206 Free article. Review.

7

Insights into genotype-phenotype correlation in pachyonychia congenita from the human intermediate filament mutation database.

McLean WH, Smith FJ, Cassidy AJ. McLean WH, et al. J Investig Dermatol Symp Proc. 2005 Oct;10(1):31-6. doi: 10.1111/j.1087-0024.2005.10205.x. J Investig Dermatol Symp Proc. 2005. PMID: 16250207 Free article. Review.

8

Keratin K6c mutations cause focal palmoplantar keratoderma.

Wilson NJ, Messenger AG, Leachman SA, O'Toole EA, Lane EB, McLean WH, Smith FJ. Wilson NJ, et al. Among authors: mclean wh. J Invest Dermatol. 2010 Feb;130(2):425-9. doi: 10.1038/jid.2009.215. Epub 2009 Jul 16. J Invest Dermatol. 2010. PMID: 19609311 Free article.

9

Effects of keratin 14 ablation on the clinical and cellular phenotype in a kindred with recessive epidermolysis bullosa simplex.

Jonkman MF, Heeres K, Pas HH, van Luyn MJ, Elema JD, Corden LD, Smith FJ, McLean WH, Ramaekers FC, Burton M, Scheffer H. Jonkman MF, et al. Among authors: mclean wh. J Invest Dermatol. 1996 Nov;107(5):764-9. doi: 10.1111/1523-1747.ep12365805. J Invest Dermatol. 1996. PMID: 8875963 Free article.

10

Plectin and human genetic disorders of the skin and muscle. The paradigm of epidermolysis bullosa with muscular dystrophy.

Uitto J, Pulkkinen L, Smith FJ, McLean WH. Uitto J, et al. Among authors: mclean wh. Exp Dermatol. 1996 Oct;5(5):237-46. doi: 10.1111/j.1600-0625.1996.tb00124.x. Exp Dermatol. 1996. PMID: 8981021 Review.

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