Hide M - Search Results

1

Predictive phenotyping of inherited ichthyosis by next-generation DNA sequencing.

Saito R, Boyce A, Hsu CK, Rashidghamat E, Hide M, Wedgeworth EK, Flohr C, Mellerio JE, McGrath JA. Saito R, et al. Among authors: hide m. Br J Dermatol. 2017 Jan;176(1):249-251. doi: 10.1111/bjd.14807. Epub 2016 Dec 7. Br J Dermatol. 2017. PMID: 27291450 No abstract available.

2

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: hide m. 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.

3

Identification of a homozygous deletion mutation in C16orf57 in a family with Clericuzio-type poikiloderma with neutropenia.

Tanaka A, Morice-Picard F, Lacombe D, Nagy N, Hide M, Taïeb A, McGrath J. Tanaka A, et al. Among authors: hide m. Am J Med Genet A. 2010 Jun;152A(6):1347-8. doi: 10.1002/ajmg.a.33455. Am J Med Genet A. 2010. PMID: 20503306 No abstract available.

4

The molecular skin pathology of familial primary localized cutaneous amyloidosis.

Tanaka A, Lai-Cheong JE, van den Akker PC, Nagy N, Millington G, Diercks GF, van Voorst Vader PC, Clements SE, Almaani N, Techanukul T, Hide M, South AP, McGrath JA. Tanaka A, et al. Among authors: hide m. Exp Dermatol. 2010 May;19(5):416-23. doi: 10.1111/j.1600-0625.2010.01083.x. Exp Dermatol. 2010. PMID: 20507362

5

Germline mutation in ATR in autosomal- dominant oropharyngeal cancer syndrome.

Tanaka A, Weinel S, Nagy N, O'Driscoll M, Lai-Cheong JE, Kulp-Shorten CL, Knable A, Carpenter G, Fisher SA, Hiragun M, Yanase Y, Hide M, Callen J, McGrath JA. Tanaka A, et al. Among authors: hide m. Am J Hum Genet. 2012 Mar 9;90(3):511-7. doi: 10.1016/j.ajhg.2012.01.007. Epub 2012 Feb 16. Am J Hum Genet. 2012. PMID: 22341969 Free PMC article.

6

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

7

Novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair.

Matsuo Y, Tanaka A, Shimomura Y, Hide M. Matsuo Y, et al. Among authors: hide m. J Dermatol. 2016 Nov;43(11):1384-1385. doi: 10.1111/1346-8138.13373. Epub 2016 Apr 20. J Dermatol. 2016. PMID: 27094727 No abstract available.

8

Presymptomatic genetic diagnosis of two siblings with hereditary angioedema, presenting with unusual normal levels of serum C4.

Kasami S, Sowa-Osako J, Fukai K, Tokimasa S, Kaga SI, Saito R, Tanaka A, Hide M, Tsuruta D. Kasami S, et al. Among authors: hide m. J Dermatol. 2018 Feb;45(2):e31-32. doi: 10.1111/1346-8138.14103. Epub 2017 Oct 23. J Dermatol. 2018. PMID: 29058329 No abstract available.

9

Rapid exacerbation of malignant melanoma during short-term discontinuation of vemurafenib.

Saito R, Iwamoto K, Tanaka Y, Kawai M, Hide M. Saito R, et al. Among authors: hide m. Australas J Dermatol. 2018 Nov;59(4):e274-e276. doi: 10.1111/ajd.12784. Epub 2018 Jan 29. Australas J Dermatol. 2018. PMID: 29380358 No abstract available.

10

Case of malignant melanoma responding to dacarbazine following nivolumab.

Saito R, Kawai M, Hirakawa K, Tanaka M, Takahagi S, Hide M. Saito R, et al. Among authors: hide m. Dermatol Ther. 2019 Mar;32(2):e12791. doi: 10.1111/dth.12791. Epub 2018 Dec 12. Dermatol Ther. 2019. PMID: 30488521 No abstract available.

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