McGrath JA - Search Results

1

Kantaputra P, Olsen B, McGrath JA. Kantaputra P, et al. Among authors: mcgrath ja. J Dermatol. 2022 May;49(5):e183-e184. doi: 10.1111/1346-8138.16313. Epub 2022 Feb 21. J Dermatol. 2022. PMID: 35191062 No abstract available.

2

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

3

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

4

Schopf-Schulz-Passarge syndrome: a rare ectodermal dysplasia with a delayed diagnosis.

Ismail FF, McGrath J, Sinclair R. Ismail FF, et al. Int J Dermatol. 2020 Feb;59(2):257-258. doi: 10.1111/ijd.14616. Epub 2019 Aug 29. Int J Dermatol. 2020. PMID: 31468502 No abstract available.

5

A truncating variant in SERPINA3, skin pustules and adult-onset immunodeficiency.

Kantaputra PN, Chuamanochan M, Kiratikanon S, Chiewchanvit S, Chaiwarith R, Intachai W, Quarto N, Tongsima S, McGrath JA, Ngamphiw C. Kantaputra PN, et al. Among authors: mcgrath ja. J Dermatol. 2021 Aug;48(8):e370-e371. doi: 10.1111/1346-8138.15942. Epub 2021 May 7. J Dermatol. 2021. PMID: 33961311 No abstract available.

6

WNT10A, dermatology and dentistry.

Doolan BJ, Onoufriadis A, Kantaputra P, McGrath JA. Doolan BJ, et al. Among authors: mcgrath ja. Br J Dermatol. 2021 Dec;185(6):1105-1111. doi: 10.1111/bjd.20601. Epub 2021 Sep 7. Br J Dermatol. 2021. PMID: 34184264 Review.

7

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

8

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.

9

A novel genodermatosis caused by mutations in plakophilin 1, a structural component of desmosomes.

McGrath JA. McGrath JA. J Dermatol. 1999 Nov;26(11):764-9. doi: 10.1111/j.1346-8138.1999.tb02089.x. J Dermatol. 1999. PMID: 10635620 Review.

10

Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory.

Takeichi T, Liu L, Fong K, Ozoemena L, McMillan JR, Salam A, Campbell P, Akiyama M, Mellerio JE, McLean WH, Simpson MA, McGrath JA. Takeichi T, et al. Among authors: mcgrath ja. Br J Dermatol. 2015 Jan;172(1):94-100. doi: 10.1111/bjd.13190. Epub 2014 Nov 19. Br J Dermatol. 2015. PMID: 24947307

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