Hsu CK - Search Results

1

Th2 response drives itch in dystrophic epidermolysis bullosa pruriginosa: A case-control study.

Papanikolaou M, Nattkemper L, Benzian-Olsson N, Liu L, Guy A, Lu H, Kadiyirire T, Hou PC, Aala W, Serrano S, Pramanik R, Walters N, Dimitrakopoulou K, Lwin S, Kalfas E, Satoc J, Laddach R, Cozzetto D, Thomas B, Kesidou E, Rashidghamat E, Orchard G, O'Toole EA, Hsu CK, Saqi M, Steinhoff M, Onoufriadis A, Yosipovitch G, Gould H, Mellerio JE, McGrath JA. Papanikolaou M, et al. Among authors: hsu ck. J Am Acad Dermatol. 2024 Mar 13:S0190-9622(24)00487-0. doi: 10.1016/j.jaad.2024.01.088. Online ahead of print. J Am Acad Dermatol. 2024. PMID: 38484894 Free article. No abstract available.

2

Demodicosis: a clinicopathological study.

Hsu CK, Hsu MM, Lee JY. Hsu CK, et al. Among authors: hsu mm. J Am Acad Dermatol. 2009 Mar;60(3):453-62. doi: 10.1016/j.jaad.2008.10.058. J Am Acad Dermatol. 2009. PMID: 19231642

3

Treatment of hereditary epidermolysis bullosa: updates and future prospects.

Hsu CK, Wang SP, Lee JY, McGrath JA. Hsu CK, et al. 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.

4

Novel indel mutation of STS underlies a new phenotype of self-healing recessive X-linked ichthyosis.

Takeichi T, Sugiura K, Hsu CK, Tanahashi K, Takama H, Simpson MA, McGrath JA, Akiyama M. Takeichi T, et al. Among authors: hsu ck. J Dermatol Sci. 2015 Sep;79(3):317-9. doi: 10.1016/j.jdermsci.2015.07.001. Epub 2015 Jul 6. J Dermatol Sci. 2015. PMID: 26169345 No abstract available.

5

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. Australas J Dermatol. 2017 Feb;58(1):58-60. doi: 10.1111/ajd.12399. Epub 2015 Sep 23. Australas J Dermatol. 2017. PMID: 26400620

6

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: hsu ck. Australas J Dermatol. 2016 May;57(2):150-3. doi: 10.1111/ajd.12407. Epub 2015 Oct 6. Australas J Dermatol. 2016. PMID: 26437686

7

Ichthyosis Prematurity Syndrome: From Fetus to Adulthood.

Lwin SM, Hsu CK, McMillan JR, Mellerio JE, McGrath JA. Lwin SM, et al. Among authors: hsu ck. JAMA Dermatol. 2016 Sep 1;152(9):1055-8. doi: 10.1001/jamadermatol.2016.1187. JAMA Dermatol. 2016. PMID: 27224495 No abstract available.

8

Ectodermal dysplasia-skin fragility syndrome resulting from a new atypical homozygous cryptic acceptor splice site mutation in PKP1.

Hsu CK, Liu L, Can PK, Kocatürk E, McMillan JR, Güngör Ş, Hürdoğan Ö, Sargan A, Degirmentepe EN, Lee JY, Simpson MA, McGrath JA. Hsu CK, et al. J Dermatol Sci. 2016 Nov;84(2):210-212. doi: 10.1016/j.jdermsci.2016.08.011. Epub 2016 Aug 11. J Dermatol Sci. 2016. PMID: 27554337 No abstract available.

9

Congenital Anonychia and Uncombable Hair Syndrome: Coinheritance of Homozygous Mutations in RSPO4 and PADI3.

Hsu CK, Romano MT, Nanda A, Rashidghamat E, Lee JYW, Huang HY, Songsantiphap C, Lee JY, Al-Ajmi H, Betz RC, Simpson MA, McGrath JA, Tziotzios C. Hsu CK, et al. J Invest Dermatol. 2017 May;137(5):1176-1179. doi: 10.1016/j.jid.2016.12.015. Epub 2017 Jan 10. J Invest Dermatol. 2017. PMID: 28087452 Free article. No abstract available.

10

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: hsu ck. 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.

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