Leigh IM - Search Results

1

Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.

Wilgoss A, Leigh IM, Barnes MR, Dopping-Hepenstal P, Eady RA, Walter JM, Kennedy CT, Kelsell DP. Wilgoss A, et al. Among authors: leigh im. J Invest Dermatol. 1999 Dec;113(6):1119-22. doi: 10.1046/j.1523-1747.1999.00792.x. J Invest Dermatol. 1999. PMID: 10594760 Free article.

2

Drug eruption or psoriasis?

Kennedy C, Leigh IM, Gold S. Kennedy C, et al. Among authors: leigh im. Br Med J. 1979 May 19;1(6174):1356-7. doi: 10.1136/bmj.1.6174.1356-e. Br Med J. 1979. PMID: 156055 Free PMC article. No abstract available.

3

Recurrent vasculitis with beta-haemolytic streptococcal infections.

Kennedy C, Leigh IM, Gold SC. Kennedy C, et al. Among authors: leigh im. Br Med J. 1978 Jun 24;1(6128):1699-700. doi: 10.1136/bmj.1.6128.1699-c. Br Med J. 1978. PMID: 418847 Free PMC article. No abstract available.

4

Systemic sclerosis with subcutaneous nodules.

Kennedy C, Leigh IM. Kennedy C, et al. Among authors: leigh im. Br J Dermatol. 1979 Jul;101(1):93-6. doi: 10.1111/j.1365-2133.1979.tb15300.x. Br J Dermatol. 1979. PMID: 475994

5

Mepacrine pigmentation in systemic lupus erythematosus. New data from an ultrastructural, biochemical and analytical electron microscopic investigation.

Leigh IM, Kennedy CT, Ramsey JD, Henderson WJ. Leigh IM, et al. Br J Dermatol. 1979 Aug;101(2):147-53. doi: 10.1111/j.1365-2133.1979.tb05599.x. Br J Dermatol. 1979. PMID: 486320

6

A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering.

Lane EB, Rugg EL, Navsaria H, Leigh IM, Heagerty AH, Ishida-Yamamoto A, Eady RA. Lane EB, et al. Among authors: leigh im. Nature. 1992 Mar 19;356(6366):244-6. doi: 10.1038/356244a0. Nature. 1992. PMID: 1372711

7

Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma).

Ishida-Yamamoto A, McGrath JA, Judge MR, Leigh IM, Lane EB, Eady RA. Ishida-Yamamoto A, et al. Among authors: leigh im. J Invest Dermatol. 1992 Jul;99(1):19-26. doi: 10.1111/1523-1747.ep12611391. J Invest Dermatol. 1992. PMID: 1376754 Free article.

8

Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locus.

al-Imara L, Richards AJ, Eady RA, Leigh IM, Farrall M, Pope FM. al-Imara L, et al. Among authors: leigh im. J Med Genet. 1992 Jun;29(6):381-2. doi: 10.1136/jmg.29.6.381. J Med Genet. 1992. PMID: 1377750 Free PMC article.

9

Intracellular expression of type VII collagen during wound healing in severe recessive dystrophic epidermolysis bullosa and normal human skin.

McGrath JA, Leigh IM, Eady RA. McGrath JA, et al. Among authors: leigh im. Br J Dermatol. 1992 Oct;127(4):312-7. doi: 10.1111/j.1365-2133.1992.tb00447.x. Br J Dermatol. 1992. PMID: 1419750

10

Epidermolysis bullosa simplex (Dowling-Meara type) is a genetic disease characterized by an abnormal keratin-filament network involving keratins K5 and K14.

Ishida-Yamamoto A, McGrath JA, Chapman SJ, Leigh IM, Lane EB, Eady RA. Ishida-Yamamoto A, et al. Among authors: leigh im. J Invest Dermatol. 1991 Dec;97(6):959-68. doi: 10.1111/1523-1747.ep12491885. J Invest Dermatol. 1991. PMID: 1721080 Free article.

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