McGrath JA - Search Results

1

New insights into hereditary angio-oedema: Molecular diagnosis and therapy.

Nagy N, Grattan CE, McGrath JA. Nagy N, et al. Among authors: mcgrath ja. Australas J Dermatol. 2010 Aug;51(3):157-62. doi: 10.1111/j.1440-0960.2010.00649.x. Australas J Dermatol. 2010. PMID: 20695852 Review.

2

Translational benefits from research on rare genodermatoses.

McGrath JA. McGrath JA. Australas J Dermatol. 2004 May;45(2):89-93. doi: 10.1111/j.1440-0960.2004.00070.x. Australas J Dermatol. 2004. PMID: 15068453 Review.

3

Inherited disorders of desmosomes.

McGrath JA. McGrath JA. Australas J Dermatol. 2005 Nov;46(4):221-9. doi: 10.1111/j.1440-0960.2005.00188.x. Australas J Dermatol. 2005. PMID: 16197419 Review.

4

Phenotype, genotype, and sustained response to anakinra in 22 patients with autoinflammatory disease associated with CIAS-1/NALP3 mutations.

Leslie KS, Lachmann HJ, Bruning E, McGrath JA, Bybee A, Gallimore JR, Roberts PF, Woo P, Grattan CE, Hawkins PN. Leslie KS, et al. Among authors: mcgrath ja. Arch Dermatol. 2006 Dec;142(12):1591-7. doi: 10.1001/archderm.142.12.1591. Arch Dermatol. 2006. PMID: 17178985

5

Filaggrin and the great epidermal barrier grief.

McGrath JA. McGrath JA. Australas J Dermatol. 2008 May;49(2):67-73; quiz 73-4. doi: 10.1111/j.1440-0960.2008.00443.x. Australas J Dermatol. 2008. PMID: 18412804 Review.

6

Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema.

Nagy N, Greaves MW, Tanaka A, McGrath JA, Grattan CE. Nagy N, et al. Among authors: mcgrath ja. J Dermatol Sci. 2009 Oct;56(1):62-4. doi: 10.1016/j.jdermsci.2009.06.013. Epub 2009 Jul 31. J Dermatol Sci. 2009. PMID: 19647418 No abstract available.

7

Blistering skin diseases: a bridge between dermatopathology and molecular biology.

Nagy N, McGrath JA. Nagy N, et al. Among authors: mcgrath ja. Histopathology. 2010 Jan;56(1):91-9. doi: 10.1111/j.1365-2559.2009.03442.x. Histopathology. 2010. PMID: 20055907 Review.

8

Revertant mosaicism in recessive dystrophic epidermolysis bullosa.

Almaani N, Nagy N, Liu L, Dopping-Hepenstal PJ, Lai-Cheong JE, Clements SE, Techanukul T, Tanaka A, Mellerio JE, McGrath JA. Almaani N, et al. Among authors: mcgrath ja. J Invest Dermatol. 2010 Jul;130(7):1937-40. doi: 10.1038/jid.2010.64. Epub 2010 Apr 1. J Invest Dermatol. 2010. PMID: 20357813 Free article. No abstract available.

9

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A.

Nagy N, Wedgeworth E, Hamada T, White JM, Hashimoto T, McGrath JA. Nagy N, et al. Among authors: mcgrath ja. J Dermatol Sci. 2010 Jun;58(3):220-2. doi: 10.1016/j.jdermsci.2010.03.012. Epub 2010 Mar 23. J Dermatol Sci. 2010. PMID: 20418069 No abstract available.

10

The molecular skin pathology of familial primary localized cutaneous amyloidosis.

Tanaka A, Lai-Cheong JE, van den Akker PC, Nagy N, Millington G, Diercks GF, van Voorst Vader PC, Clements SE, Almaani N, Techanukul T, Hide M, South AP, McGrath JA. Tanaka A, et al. Among authors: mcgrath ja. Exp Dermatol. 2010 May;19(5):416-23. doi: 10.1111/j.1600-0625.2010.01083.x. Exp Dermatol. 2010. PMID: 20507362

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