McGrath JA - Search Results

1

A review of genotrichoses and hair pathology associated with inherited skin diseases.

Doolan BJ, Rayinda T, Chiu FP, McGrath JA, Onoufriadis A. Doolan BJ, et al. Among authors: mcgrath ja. Br J Dermatol. 2023 Jul 17;189(2):154-160. doi: 10.1093/bjd/ljad102. Br J Dermatol. 2023. PMID: 36978220 Review.

2

Preimplantation genetic diagnosis of severe inherited skin diseases.

McGrath JA, Handyside AH. McGrath JA, et al. Exp Dermatol. 1998 Apr-Jun;7(2-3):65-72. doi: 10.1111/j.1600-0625.1998.tb00305.x. Exp Dermatol. 1998. PMID: 9583745 Review.

3

Prenatal diagnosis for severe inherited skin disorders: 25 years' experience.

Fassihi H, Eady RA, Mellerio JE, Ashton GH, Dopping-Hepenstal PJ, Denyer JE, Nicolaides KH, Rodeck CH, McGrath JA. Fassihi H, et al. Among authors: mcgrath ja. Br J Dermatol. 2006 Jan;154(1):106-13. doi: 10.1111/j.1365-2133.2005.07012.x. Br J Dermatol. 2006. PMID: 16403102

4

Novel truncating mutations in PKP1 and DSP cause similar skin phenotypes in two Brazilian families.

Tanaka A, Lai-Cheong JE, Café ME, Gontijo B, Salomão PR, Pereira L, McGrath JA. Tanaka A, et al. Among authors: mcgrath ja. Br J Dermatol. 2009 Mar;160(3):692-7. doi: 10.1111/j.1365-2133.2008.08900.x. Epub 2008 Oct 21. Br J Dermatol. 2009. PMID: 19016709

5

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

6

Molecular basis of EEC (ectrodactyly, ectodermal dysplasia, clefting) syndrome: five new mutations in the DNA-binding domain of the TP63 gene and genotype-phenotype correlation.

Clements SE, Techanukul T, Coman D, Mellerio JE, McGrath JA. Clements SE, et al. Among authors: mcgrath ja. Br J Dermatol. 2010 Jan;162(1):201-7. doi: 10.1111/j.1365-2133.2009.09496.x. Epub 2009 Nov 9. Br J Dermatol. 2010. PMID: 19903181

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

Skin differences based on age and chronicity of ultraviolet exposure: results from a gene expression profiling study.

McGrath JA, Robinson MK, Binder RL. McGrath JA, et al. Br J Dermatol. 2012 Jun;166 Suppl 2:9-15. doi: 10.1111/j.1365-2133.2012.10860.x. Br J Dermatol. 2012. PMID: 22670613

10

Clinical features and WNT10A mutations in seven unrelated cases of Schöpf-Schulz-Passarge syndrome.

Tziotzios C, Petrof G, Liu L, Verma A, Wedgeworth EK, Mellerio JE, McGrath JA. Tziotzios C, et al. Among authors: mcgrath ja. Br J Dermatol. 2014 Nov;171(5):1211-4. doi: 10.1111/bjd.13158. Epub 2014 Oct 15. Br J Dermatol. 2014. PMID: 24902757

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