McGrath JA - Search Results

1

Frontal fibrosing alopecia: a descriptive cross-sectional study of 711 cases in female patients from the UK.

McSweeney SM, Christou EAA, Dand N, Boalch A, Holmes S, Harries M, Palamaras I, Cunningham F, Parkins G, Kaur M, Farrant P, McDonagh A, Messenger A, Jones J, Jolliffe V, Ali I, Ardern-Jones M, Mitchell C, Burrows N, Atkar R, Banfield C, Alexandroff A, Champagne C, Cooper HL, Patel GK, Macbeth A, Page M, Bryden A, Mowbray M, Wahie S, Armstrong K, Cooke N, Goodfield M, Man I, de Berker D, Dunnil G, Takwale A, Rao A, Siah TW, Sinclair R, Wade MS, Bhargava K, Fenton DA, McGrath JA, Tziotzios C. McSweeney SM, et al. Among authors: mcgrath ja. Br J Dermatol. 2020 Dec;183(6):1136-1138. doi: 10.1111/bjd.19399. Epub 2020 Sep 10. Br J Dermatol. 2020. PMID: 32652611 No abstract available.

2

Epidermolysis bullosa simplex Dowling-Meara: troublesome blistering and pruritus in an adult patient.

McGrath JA, Burrows NP, Russell Jones R, Eady RA. McGrath JA, et al. Dermatology. 1993;186(1):68-71. doi: 10.1159/000247306. Dermatology. 1993. PMID: 8435522

3

Expression and glycosylation of MUC1 in epidermolysis bullosa-associated and sporadic cutaneous squamous cell carcinomas.

Cooper HL, Cook IS, Theaker JM, Mallipeddi R, McGrath J, Friedmann P, Healy E. Cooper HL, et al. Br J Dermatol. 2004 Sep;151(3):540-5. doi: 10.1111/j.1365-2133.2004.06075.x. Br J Dermatol. 2004. PMID: 15377338

4

Transient bullous dermolysis of the newborn in three generations.

Fassihi H, Diba VC, Wessagowit V, Dopping-Hepenstal PJ, Jones CA, Burrows NP, McGrath JA. Fassihi H, et al. Among authors: mcgrath ja. Br J Dermatol. 2005 Nov;153(5):1058-63. doi: 10.1111/j.1365-2133.2005.06873.x. Br J Dermatol. 2005. PMID: 16225626

5

A novel mutation in the VDR gene in hereditary vitamin D-resistant rickets.

Arita K, Nanda A, Wessagowit V, Akiyama M, Alsaleh QA, McGrath JA. Arita K, et al. Among authors: mcgrath ja. Br J Dermatol. 2008 Jan;158(1):168-71. doi: 10.1111/j.1365-2133.2007.08232.x. Epub 2007 Oct 26. Br J Dermatol. 2008. PMID: 17970811 No abstract available.

6

Epidermolysis bullosa pruriginosa in association with lichen planopilaris.

Almaani N, Liu L, Perez A, Robson A, Mellerio JE, McGrath JA. Almaani N, et al. Among authors: mcgrath ja. Clin Exp Dermatol. 2009 Dec;34(8):e825-8. doi: 10.1111/j.1365-2230.2009.03568.x. Clin Exp Dermatol. 2009. PMID: 20055845

7

Desmosomal genodermatoses.

Petrof G, Mellerio JE, McGrath JA. Petrof G, et al. Among authors: mcgrath ja. Br J Dermatol. 2012 Jan;166(1):36-45. doi: 10.1111/j.1365-2133.2011.10640.x. Br J Dermatol. 2012. PMID: 21929534 Review.

8

Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology.

Clements SE, Techanukul T, Lai-Cheong JE, Mee JB, South AP, Pourreyron C, Burrows NP, Mellerio JE, McGrath JA. Clements SE, et al. Among authors: mcgrath ja. Br J Dermatol. 2012 Jul;167(1):134-44. doi: 10.1111/j.1365-2133.2012.10888.x. Epub 2012 May 14. Br J Dermatol. 2012. PMID: 22329826

9

Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome.

Lai-Cheong JE, Sethuraman G, Ramam M, Stone K, Simpson MA, McGrath JA. Lai-Cheong JE, et al. Among authors: mcgrath ja. Br J Dermatol. 2012 Aug;167(2):440-2. doi: 10.1111/j.1365-2133.2012.11115.x. Br J Dermatol. 2012. PMID: 22835024

10

Fibroblast cell therapy enhances initial healing in recessive dystrophic epidermolysis bullosa wounds: results of a randomized, vehicle-controlled trial.

Petrof G, Martinez-Queipo M, Mellerio JE, Kemp P, McGrath JA. Petrof G, et al. Among authors: mcgrath ja. Br J Dermatol. 2013 Nov;169(5):1025-33. doi: 10.1111/bjd.12599. Br J Dermatol. 2013. PMID: 24032424 Clinical Trial.

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