McGrath JA - Search Results

1

SERPINA1, generalized pustular psoriasis, and adult-onset immunodeficiency.

Kantaputra P, Chaowattanapanit S, Kiratikanon S, Chaiwarith R, Choonhakarn C, Intachai W, Quarto N, Tongsima S, Ketudat Cairns JR, Ngamphiw C, McGrath JA, Chuamanochan M. Kantaputra P, et al. Among authors: mcgrath ja. J Dermatol. 2021 Oct;48(10):1597-1601. doi: 10.1111/1346-8138.16081. Epub 2021 Aug 12. J Dermatol. 2021. PMID: 34390020

2

Prenatal diagnosis for inherited skin diseases.

Ashton GH, Eady RA, McGrath JA. Ashton GH, et al. Among authors: mcgrath ja. Clin Dermatol. 2000 Nov-Dec;18(6):643-8. doi: 10.1016/s0738-081x(00)00153-x. Clin Dermatol. 2000. PMID: 11173198 Review. No abstract available.

3

Gene mutations, great expectations.

McGrath JA. McGrath JA. Clin Dermatol. 2001 Jan-Feb;19(1):59-64. doi: 10.1016/s0738-081x(00)00213-3. Clin Dermatol. 2001. PMID: 11369489 Review. No abstract available.

4

Psoriasis bullosa acquisita.

Morris SD, Mallipeddi R, Oyama N, Gratian MJ, Harman KE, Bhogal BS, Black MM, Eady RA, Hashimoto T, McGrath JA. Morris SD, et al. Among authors: mcgrath ja. Clin Exp Dermatol. 2002 Nov;27(8):665-9. doi: 10.1046/j.1365-2230.2002.01100.x. Clin Exp Dermatol. 2002. PMID: 12472542

5

Heterozygous mutation in the SAM domain of p63 underlies Rapp-Hodgkin ectodermal dysplasia.

Kantaputra PN, Hamada T, Kumchai T, McGrath JA. Kantaputra PN, et al. Among authors: mcgrath ja. J Dent Res. 2003 Jun;82(6):433-7. doi: 10.1177/154405910308200606. J Dent Res. 2003. PMID: 12766194

6

Target proteins in inherited and acquired blistering skin disorders.

Fassihi H, Wong T, Wessagowit V, McGrath JA, Mellerio JE. Fassihi H, et al. Among authors: mcgrath ja. Clin Exp Dermatol. 2006 Mar;31(2):252-9. doi: 10.1111/j.1365-2230.2006.02065.x. Clin Exp Dermatol. 2006. PMID: 16487105 Review.

7

New insight into mechanisms of pruritus from molecular studies on familial primary localized cutaneous amyloidosis.

Tanaka A, Arita K, Lai-Cheong JE, Palisson F, Hide M, McGrath JA. Tanaka A, et al. Among authors: mcgrath ja. Br J Dermatol. 2009 Dec;161(6):1217-24. doi: 10.1111/j.1365-2133.2009.09311.x. Epub 2009 May 26. Br J Dermatol. 2009. PMID: 19663869 Review.

8

MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvans.

Fong K, Wedgeworth EK, Lai-Cheong JE, Tosi I, Mellerio JE, Powell AM, McGrath JA. Fong K, et al. Among authors: mcgrath ja. Clin Exp Dermatol. 2012 Aug;37(6):631-4. doi: 10.1111/j.1365-2230.2011.04288.x. Clin Exp Dermatol. 2012. PMID: 22816986

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

A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutations.

Vahlquist A, Virtanen M, Hellström-Pigg M, Dragomir A, Ryberg K, Wilson NJ, Östman--Smith I, Lu L, McGrath JA, Smith FJ. Vahlquist A, et al. Among authors: mcgrath ja. Clin Exp Dermatol. 2014 Jan;39(1):30-4. doi: 10.1111/ced.12226. Clin Exp Dermatol. 2014. PMID: 24341478

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