McGrath JA - Search Results

1

Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndrome.

Whittock NV, Haftek M, Angoulvant N, Wolf F, Perrot H, Eady RA, McGrath JA. Whittock NV, et al. Among authors: mcgrath ja. J Invest Dermatol. 2000 Sep;115(3):368-74. doi: 10.1046/j.1523-1747.2000.00082.x. J Invest Dermatol. 2000. PMID: 10951270 Free article.

2

Oral and gastrointestinal manifestations of epidermolysis bullosa.

Travis SP, McGrath JA, Turnbull AJ, Schofield OM, Chan O, O'Connor AF, Mayou B, Eady RA, Thompson RP. Travis SP, et al. Among authors: mcgrath ja. Lancet. 1992 Dec 19-26;340(8834-8835):1505-6. doi: 10.1016/0140-6736(92)92759-9. Lancet. 1992. PMID: 1361600

3

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: mcgrath ja. J Invest Dermatol. 1992 Jul;99(1):19-26. doi: 10.1111/1523-1747.ep12611391. J Invest Dermatol. 1992. PMID: 1376754 Free article.

4

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. Br J Dermatol. 1992 Oct;127(4):312-7. doi: 10.1111/j.1365-2133.1992.tb00447.x. Br J Dermatol. 1992. PMID: 1419750

5

Mitten deformity in severe generalized recessive dystrophic epidermolysis bullosa: histological, immunofluorescence, and ultrastructural study.

McGrath JA, O'Grady A, Mayou BJ, Eady RA. McGrath JA, et al. J Cutan Pathol. 1992 Oct;19(5):385-9. doi: 10.1111/j.1600-0560.1992.tb00610.x. J Cutan Pathol. 1992. PMID: 1474191

6

Expression of mutant p53 gene in squamous carcinoma arising in patients with recessive dystrophic epidermolysis bullosa.

Slater SD, McGrath JA, Hobbs C, Eady RA, McKee PH. Slater SD, et al. Among authors: mcgrath ja. Histopathology. 1992 Mar;20(3):237-41. doi: 10.1111/j.1365-2559.1992.tb00962.x. Histopathology. 1992. PMID: 1563710

7

Epidermolysis bullosa complicated by squamous cell carcinoma: report of 10 cases.

McGrath JA, Schofield OM, Mayou BJ, McKee PH, Eady RA. McGrath JA, et al. J Cutan Pathol. 1992 Apr;19(2):116-23. doi: 10.1111/j.1600-0560.1992.tb01352.x. J Cutan Pathol. 1992. PMID: 1597567

8

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

9

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: mcgrath ja. J Invest Dermatol. 1991 Dec;97(6):959-68. doi: 10.1111/1523-1747.ep12491885. J Invest Dermatol. 1991. PMID: 1721080 Free article.

10

Metastatic squamous cell carcinoma resembling angiosarcoma complicating dystrophic epidermolysis bullosa.

McGrath JA, Schofield OM, Mayou BJ, McKee PH, Eady RA. McGrath JA, et al. Dermatologica. 1991;182(4):235-8. doi: 10.1159/000247803. Dermatologica. 1991. PMID: 1884860

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