McGrath JA - Search Results

1

Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations.

Szczecinska W, Nesteruk D, Wertheim-Tysarowska K, Greenblatt DT, Baty D, Browne F, Liu L, Ozoemena L, Terron-Kwiatkowski A, McGrath JA, Mellerio JE, Morton J, Woźniak K, Kowalewski C, Has C, Moss C. Szczecinska W, et al. Among authors: mcgrath ja. Br J Dermatol. 2014 Nov;171(5):1206-10. doi: 10.1111/bjd.12964. Epub 2014 Oct 20. Br J Dermatol. 2014. PMID: 24628291

2

Epidermolysis bullosa simplex (Dowling-Meara). A clinicopathological review.

McGrath JA, Ishida-Yamamoto A, Tidman MJ, Heagerty AH, Schofield OM, Eady RA. McGrath JA, et al. Br J Dermatol. 1992 May;126(5):421-30. doi: 10.1111/j.1365-2133.1992.tb11813.x. Br J Dermatol. 1992. PMID: 1610681

3

Epidermolysis bullosa pruriginosa: dystrophic epidermolysis bullosa with distinctive clinicopathological features.

McGrath JA, Schofield OM, Eady RA. McGrath JA, et al. Br J Dermatol. 1994 May;130(5):617-25. doi: 10.1111/j.1365-2133.1994.tb13109.x. Br J Dermatol. 1994. PMID: 8204470

4

A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk.

McGrath JA, Kivirikko S, Ciatti S, Moss C, Dunnill GS, Eady RA, Rodeck CH, Christiano AM, Uitto J. McGrath JA, et al. Genomics. 1995 Sep 1;29(1):282-4. doi: 10.1006/geno.1995.1246. Genomics. 1995. PMID: 8530087

5

A recurrent homozygous nonsense mutation within the LAMA3 gene as a cause of Herlitz junctional epidermolysis bullosa in patients of Pakistani ancestry: evidence for a founder effect.

McGrath JA, Kivirikko S, Ciatti S, Moss C, Christiano AM, Uitto J. McGrath JA, et al. J Invest Dermatol. 1996 Apr;106(4):781-4. doi: 10.1111/1523-1747.ep12346349. J Invest Dermatol. 1996. PMID: 8618022 Free article.

6

First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus sampling.

McGrath JA, Dunnill MG, Christiano AM, Lake BD, Atherton DJ, Rodeck CH, Pope FM, Eady RA, Uitto J. McGrath JA, et al. Br J Dermatol. 1996 Apr;134(4):734-9. doi: 10.1111/j.1365-2133.1996.tb06981.x. Br J Dermatol. 1996. PMID: 8733382

7

A recurrent laminin 5 mutation in British patients with lethal (Herlitz) junctional epidermolysis bullosa: evidence for a mutational hotspot rather than propagation of an ancestral allele.

Ashton GH, Mellerio JE, Dunnill MG, Pulkkinen L, Christiano AM, Uitto J, Eady RA, McGrath JA. Ashton GH, et al. Among authors: mcgrath ja. Br J Dermatol. 1997 May;136(5):674-7. Br J Dermatol. 1997. PMID: 9205497

8

Immunohistochemical analysis of the skin in junctional epidermolysis bullosa using laminin 5 chain specific antibodies is of limited value in predicting the underlying gene mutation.

McMillan JR, McGrath JA, Pulkkinen L, Kon A, Burgeson RE, Ortonne JP, Meneguzzi G, Uitto J, Eady RA. McMillan JR, et al. Among authors: mcgrath ja. Br J Dermatol. 1997 Jun;136(6):817-22. Br J Dermatol. 1997. PMID: 9217810

9

Recurrent mutations in the type VII collagen gene (COL7A1) in patients with recessive dystrophic epidermolysis bullosa.

Mellerio JE, Dunnill MG, Allison W, Ashton GH, Christiano AM, Uitto J, Eady RA, McGrath JA. Mellerio JE, et al. Among authors: mcgrath ja. J Invest Dermatol. 1997 Aug;109(2):246-9. doi: 10.1111/1523-1747.ep12319792. J Invest Dermatol. 1997. PMID: 9242516 Free article.

10

Novel mutations in the LAMB3 gene shared by two Japanese unrelated families with Herlitz junctional epidermolysis bullosa, and their application for prenatal testing.

Takizawa Y, Shimizu H, Pulkkinen L, Hiraoka Y, McGrath JA, Suzumori K, Aiso S, Uitto J, Nishikawa T. Takizawa Y, et al. Among authors: mcgrath ja. J Invest Dermatol. 1998 Feb;110(2):174-8. doi: 10.1046/j.1523-1747.1998.00105.x. J Invest Dermatol. 1998. PMID: 9457915 Free article.

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