Nagy N - Search Results

1

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

Nagy N, Grattan CE, McGrath JA. Nagy N, et al. 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

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: nagy n. Exp Dermatol. 2010 May;19(5):416-23. doi: 10.1111/j.1600-0625.2010.01083.x. Exp Dermatol. 2010. PMID: 20507362

3

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. 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.

4

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

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

5

Germline mutation in ATR in autosomal- dominant oropharyngeal cancer syndrome.

Tanaka A, Weinel S, Nagy N, O'Driscoll M, Lai-Cheong JE, Kulp-Shorten CL, Knable A, Carpenter G, Fisher SA, Hiragun M, Yanase Y, Hide M, Callen J, McGrath JA. Tanaka A, et al. Among authors: nagy n. Am J Hum Genet. 2012 Mar 9;90(3):511-7. doi: 10.1016/j.ajhg.2012.01.007. Epub 2012 Feb 16. Am J Hum Genet. 2012. PMID: 22341969 Free PMC article.

6

Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropenia.

Tanaka A, Morice-Picard F, Lacombe D, Nagy N, Hide M, Taïeb A, McGrath J. Tanaka A, et al. Among authors: nagy n. Am J Med Genet A. 2010 Jun;152A(6):1347-8. doi: 10.1002/ajmg.a.33455. Am J Med Genet A. 2010. PMID: 20503306 No abstract available.

7

HB-EGF induces COL7A1 expression in keratinocytes and fibroblasts: possible mechanism underlying allogeneic fibroblast therapy in recessive dystrophic epidermolysis Bullosa.

Nagy N, Almaani N, Tanaka A, Lai-Cheong JE, Techanukul T, Mellerio JE, McGrath JA. Nagy N, et al. J Invest Dermatol. 2011 Aug;131(8):1771-4. doi: 10.1038/jid.2011.85. Epub 2011 Apr 7. J Invest Dermatol. 2011. PMID: 21471992 Free article. No abstract available.

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: nagy n. 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

Common IL-31 gene haplotype associated with non-atopic eczema is not implicated in epidermolysis bullosa pruriginosa.

Nagy N, Tanaka A, Techanukul T, McGrath JA. Nagy N, et al. Acta Derm Venereol. 2010 Nov;90(6):631-2. doi: 10.2340/00015555-0958. Acta Derm Venereol. 2010. PMID: 21057749 Free article. No abstract available.

10

Intra-familial variability of ectodermal defects associated with WNT10A mutations.

Wedgeworth EK, Nagy N, White JM, Pembroke AC, McGrath JA. Wedgeworth EK, et al. Among authors: nagy n. Acta Derm Venereol. 2011 May;91(3):346-7. doi: 10.2340/00015555-1028. Acta Derm Venereol. 2011. PMID: 21279306 Free article. No abstract available.

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