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Dermatological manifestations of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis (POIKTMP): a case series of 28 patients.
Chasseuil E, McGrath JA, Seo A, Balguerie X, Bodak N, Chasseuil H, Denis-Musquer M, Goldenberg A, Goussot R, Irvine AD, Khumalo NP, King MC, Küry S, Lipsker D, Mallet S, Mayosi BM, Nanda A, Puzenat E, Salort-Campana E, Sidbury R, Shimamura A, Bézieau S, Mercier S, Barbarot S. Chasseuil E, et al. Among authors: mcgrath ja. Br J Dermatol. 2019 Oct;181(4):862-864. doi: 10.1111/bjd.17996. Epub 2019 Apr 10. Br J Dermatol. 2019. PMID: 30972747 No abstract available.
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
Unusual molecular findings in Kindler syndrome.
Arita K, Wessagowit V, Inamadar AC, Palit A, Fassihi H, Lai-Cheong JE, Pourreyron C, South AP, McGrath JA. Arita K, et al. Among authors: mcgrath ja. Br J Dermatol. 2007 Dec;157(6):1252-6. doi: 10.1111/j.1365-2133.2007.08159.x. Epub 2007 Sep 13. Br J Dermatol. 2007. PMID: 17854379 Review.
Autosomal dominant junctional epidermolysis bullosa.
Almaani N, Liu L, Dopping-Hepenstal PJ, Lovell PA, Lai-Cheong JE, Graham RM, Mellerio JE, McGrath JA. Almaani N, et al. Among authors: mcgrath ja. Br J Dermatol. 2009 May;160(5):1094-7. doi: 10.1111/j.1365-2133.2008.08977.x. Epub 2009 Dec 16. Br J Dermatol. 2009. PMID: 19120338
Kindler syndrome: a focal adhesion genodermatosis.
Lai-Cheong JE, Tanaka A, Hawche G, Emanuel P, Maari C, Taskesen M, Akdeniz S, Liu L, McGrath JA. Lai-Cheong JE, et al. Among authors: mcgrath ja. Br J Dermatol. 2009 Feb;160(2):233-42. doi: 10.1111/j.1365-2133.2008.08976.x. Epub 2008 Dec 11. Br J Dermatol. 2009. PMID: 19120339 Review.
696 results