Moss C - Search Results

1

Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12.

Moss C, Srinivas SM, Sarveswaran N, Nahorski M, Gowda VK, Browne FM, Woods G. Moss C, et al. Br J Dermatol. 2018 Nov;179(5):1135-1140. doi: 10.1111/bjd.16893. Epub 2018 Sep 16. Br J Dermatol. 2018. PMID: 29949203

2

Human piebaldism: relationship between phenotype and site of kit gene mutation.

Ward KA, Moss C, Sanders DS. Ward KA, et al. Among authors: moss c. Br J Dermatol. 1995 Jun;132(6):929-35. doi: 10.1111/j.1365-2133.1995.tb16951.x. Br J Dermatol. 1995. PMID: 7544995

3

The cardio-facio-cutaneous syndrome: a manifestation of the Noonan syndrome?

Ward KA, Moss C, McKeown C. Ward KA, et al. Among authors: moss c. Br J Dermatol. 1994 Aug;131(2):270-4. doi: 10.1111/j.1365-2133.1994.tb08504.x. Br J Dermatol. 1994. PMID: 7917994

4

Evidence for genetic homogeneity of Setleis' syndrome and focal facial dermal dysplasia.

Ward KA, Moss C. Ward KA, et al. Among authors: moss c. Br J Dermatol. 1994 May;130(5):645-9. doi: 10.1111/j.1365-2133.1994.tb13113.x. Br J Dermatol. 1994. PMID: 8204474

5

What is segmental neurofibromatosis?

Moss C, Green SH. Moss C, et al. Br J Dermatol. 1994 Jan;130(1):106-10. doi: 10.1111/j.1365-2133.1994.tb06893.x. Br J Dermatol. 1994. PMID: 8305298 Review.

6

A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe disease.

Batta K, Rugg EL, Wilson NJ, West N, Goodyear H, Lane EB, Gratian M, Dopping-Hepenstal P, Moss C, Eady RA. Batta K, et al. Among authors: moss c. Br J Dermatol. 2000 Sep;143(3):621-7. doi: 10.1111/j.1365-2133.2000.03722.x. Br J Dermatol. 2000. PMID: 10971341

7

Segmental pigmentation disorder--response.

Browne F, Taibjee SM, Moss C. Browne F, et al. Among authors: moss c. Br J Dermatol. 2011 Jan;164(1):225-6; author reply 226-7. doi: 10.1111/j.1365-2133.2010.10074.x. Epub 2010 Nov 29. Br J Dermatol. 2011. PMID: 20874792 No abstract available.

8

Umbilical discharge: the acid test.

Browne F, Parashar K, Ogboli M, Moss C. Browne F, et al. Among authors: moss c. Arch Dis Child. 2011 Jun;96(6):512. doi: 10.1136/adc.2010.205658. Epub 2011 Apr 20. Arch Dis Child. 2011. PMID: 21508057 No abstract available.

9

A congenital smooth muscle hamartoma masquerading as a reticulate vascular naevus.

Vivehanantha S, Browne F, Bowen C, Brundler MA, Hughes J, Moss C, Taibjee SM. Vivehanantha S, et al. Among authors: moss c. Clin Exp Dermatol. 2013 Oct;38(7):751-3. doi: 10.1111/ced.12137. Epub 2013 Jun 13. Clin Exp Dermatol. 2013. PMID: 23758134

10

Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutations.

Szczecinska W, Nesteruk D, Wertheim-Tysarowska K, Greenblatt DT, Baty D, Browne F, Liu L, Ozoemena L, Terron-Kwiatkowski A, McGrath JA, Mellerio JE, Morton J, Woźniak K, Kowalewski C, Has C, Moss C. Szczecinska W, et al. Among authors: moss c. Br J Dermatol. 2014 Nov;171(5):1206-10. doi: 10.1111/bjd.12964. Epub 2014 Oct 20. Br J Dermatol. 2014. PMID: 24628291

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