McGrath JA - Search Results

1

Treatment of hereditary epidermolysis bullosa: updates and future prospects.

Hsu CK, Wang SP, Lee JY, McGrath JA. Hsu CK, et al. Among authors: mcgrath ja. Am J Clin Dermatol. 2014 Feb;15(1):1-6. doi: 10.1007/s40257-013-0059-z. Am J Clin Dermatol. 2014. PMID: 24402870 Review.

2

Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex.

Lee JYW, Liu L, Hsu CK, Aristodemou S, Ozoemena L, Ogboli M, Moss C, Martinez AE, Mellerio JE, McGrath JA. Lee JYW, et al. Among authors: mcgrath ja. J Invest Dermatol. 2017 Jun;137(6):1378-1380. doi: 10.1016/j.jid.2017.01.004. Epub 2017 Jan 19. J Invest Dermatol. 2017. PMID: 28111128 Free article. No abstract available.

3

Plectin Missense Mutation p.Leu319Pro in the Pathogenesis of Autosomal Recessive Epidermolysis Bullosa Simplex.

Tu WT, Chen PC, Hou PC, Huang HY, Wang JY, Chao SC, Lee JY, McGrath JA, Natsuga K, Hsu CK. Tu WT, et al. Among authors: mcgrath ja. Acta Derm Venereol. 2020 Aug 18;100(15):adv00242. doi: 10.2340/00015555-3600. Acta Derm Venereol. 2020. PMID: 32725257 Free PMC article.

4

A de novo COL17A1 splice-site mutation causing a 7-bp deletion in a Taiwanese patient with junctional epidermolysis bullosa.

Hou PC, Tu WT, Chen PC, Guevara BEK, Yen YF, Huang HY, Lee JY, Tang MJ, Kuo PL, Mcgrath JA, Hsu CK. Hou PC, et al. Among authors: mcgrath ja. Eur J Dermatol. 2021 Apr 1;31(2):267-269. doi: 10.1684/ejd.2021.4011. Eur J Dermatol. 2021. PMID: 34001479 No abstract available.

5

Complexity of Transcriptional and Translational Interference of Laminin-332 Subunits in Junctional Epidermolysis Bullosa with LAMB3 Mutations.

Hou PC, Natsuga K, Tu WT, Huang HY, Chen B, Chen LY, Chen WR, Hong YK, Tang YA, Lee JY, Chen PC, Sun HS, McGrath JA, Hsu CK. Hou PC, et al. Among authors: mcgrath ja. Acta Derm Venereol. 2021 Aug 24;101(8):adv00522. doi: 10.2340/00015555-3874. Acta Derm Venereol. 2021. PMID: 34231856 Free PMC article. No abstract available.

6

Investigational Treatments for Epidermolysis Bullosa.

Hou PC, Wang HT, Abhee S, Tu WT, McGrath JA, Hsu CK. Hou PC, et al. Among authors: mcgrath ja. Am J Clin Dermatol. 2021 Nov;22(6):801-817. doi: 10.1007/s40257-021-00626-3. Epub 2021 Jul 22. Am J Clin Dermatol. 2021. PMID: 34292508 Review.

7

Current topics in Epidermolysis bullosa: Pathophysiology and therapeutic challenges.

Natsuga K, Shinkuma S, Hsu CK, Fujita Y, Ishiko A, Tamai K, McGrath JA. Natsuga K, et al. Among authors: mcgrath ja. J Dermatol Sci. 2021 Dec;104(3):164-176. doi: 10.1016/j.jdermsci.2021.11.004. J Dermatol Sci. 2021. PMID: 34916041 Review.

8

Plasma metabolomic profiling reflects the malnourished and chronic inflammatory state in recessive dystrophic epidermolysis bullosa.

Chen YF, Lu HC, Hou PC, Lin YC, Aala WJ, Onoufriadis A, McGrath JA, Chen YL, Hsu CK. Chen YF, et al. Among authors: mcgrath ja. J Dermatol Sci. 2022 Aug;107(2):82-88. doi: 10.1016/j.jdermsci.2022.07.006. Epub 2022 Jul 13. J Dermatol Sci. 2022. PMID: 35909063

9

Systematised naevus sebaceus resulting from post-zygotic mutation in HRAS.

Hsu CK, Saito R, Nanda A, Rashidghamat E, Al-Ajmi H, Lee JY, Hide M, McGrath JA. Hsu CK, et al. Among authors: mcgrath ja. Australas J Dermatol. 2017 Feb;58(1):58-60. doi: 10.1111/ajd.12399. Epub 2015 Sep 23. Australas J Dermatol. 2017. PMID: 26400620

10

Improved molecular diagnosis of the common recurrent intragenic deletion mutation in IKBKG in a Filipino family with incontinentia pigmenti.

Guevara BE, Hsu CK, Liu L, Feast A, Alabado KL, Lacuesta MP, Lee JY, McGrath JA. Guevara BE, et al. Among authors: mcgrath ja. Australas J Dermatol. 2016 May;57(2):150-3. doi: 10.1111/ajd.12407. Epub 2015 Oct 6. Australas J Dermatol. 2016. PMID: 26437686

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