Moss C - Search Results

1

Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLG.

Cuell A, Bansal N, Cole T, Kaur MR, Lee J, Loffeld A, Moss C, O'Donnell M, Takeichi T, Thind CK, McGrath JA. Cuell A, et al. Among authors: moss c. Clin Exp Dermatol. 2015 Dec;40(8):860-4. doi: 10.1111/ced.12702. Epub 2015 Jul 14. Clin Exp Dermatol. 2015. PMID: 26179221

2

A homozygous nonsense mutation in the alpha 3 chain gene of laminin 5 (LAMA3) in Herlitz junctional epidermolysis bullosa: prenatal exclusion in a fetus at risk.

McGrath JA, Kivirikko S, Ciatti S, Moss C, Dunnill GS, Eady RA, Rodeck CH, Christiano AM, Uitto J. McGrath JA, et al. Among authors: moss c. Genomics. 1995 Sep 1;29(1):282-4. doi: 10.1006/geno.1995.1246. Genomics. 1995. PMID: 8530087

3

A recurrent homozygous nonsense mutation within the LAMA3 gene as a cause of Herlitz junctional epidermolysis bullosa in patients of Pakistani ancestry: evidence for a founder effect.

McGrath JA, Kivirikko S, Ciatti S, Moss C, Christiano AM, Uitto J. McGrath JA, et al. Among authors: moss c. J Invest Dermatol. 1996 Apr;106(4):781-4. doi: 10.1111/1523-1747.ep12346349. J Invest Dermatol. 1996. PMID: 8618022 Free article.

4

Dominant dystrophic epidermolysis bullosa presenting as familial nail dystrophy.

Dharma B, Moss C, McGrath JA, Mellerio JE, Ilchyshyn A. Dharma B, et al. Among authors: moss c. Clin Exp Dermatol. 2001 Jan;26(1):93-6. Clin Exp Dermatol. 2001. PMID: 11260188

5

Mild ichthyosis in a 4-year-old boy with multiple sulphatase deficiency.

Loffeld A, Gray RG, Green SH, Roper HP, Moss C. Loffeld A, et al. Among authors: moss c. Br J Dermatol. 2002 Aug;147(2):353-5. doi: 10.1046/j.1365-2133.2002.04776.x. Br J Dermatol. 2002. PMID: 12174111 Review.

6

Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.

Ashton GH, McLean WH, South AP, Oyama N, Smith FJ, Al-Suwaid R, Al-Ismaily A, Atherton DJ, Harwood CA, Leigh IM, Moss C, Didona B, Zambruno G, Patrizi A, Eady RA, McGrath JA. Ashton GH, et al. Among authors: moss c. J Invest Dermatol. 2004 Jan;122(1):78-83. doi: 10.1046/j.0022-202X.2003.22136.x. J Invest Dermatol. 2004. PMID: 14962093 Free article.

7

Complete paternal uniparental isodisomy of chromosome 1 resulting in Herlitz junctional epidermolysis bullosa.

Fassihi H, Wessagowit V, Ashton GH, Moss C, Ward R, Denyer J, Mellerio JE, McGrath JA. Fassihi H, et al. Among authors: moss c. Clin Exp Dermatol. 2005 Jan;30(1):71-4. doi: 10.1111/j.1365-2230.2004.01660.x. Clin Exp Dermatol. 2005. PMID: 15663509

8

Seasonal occurrence of impetigo: a retrospective 8-year review (1996-2003).

Loffeld A, Davies P, Lewis A, Moss C. Loffeld A, et al. Among authors: moss c. Clin Exp Dermatol. 2005 Sep;30(5):512-4. doi: 10.1111/j.1365-2230.2005.01847.x. Clin Exp Dermatol. 2005. PMID: 16045681

9

Two families with Greither's syndrome caused by a keratin 1 mutation.

Gach JE, Munro CS, Lane EB, Wilson NJ, Moss C. Gach JE, et al. Among authors: moss c. J Am Acad Dermatol. 2005 Nov;53(5 Suppl 1):S225-30. doi: 10.1016/j.jaad.2005.01.139. J Am Acad Dermatol. 2005. PMID: 16227096

10

Retrospective diagnosis of Kindler syndrome in a 37-year-old man.

Thomson MA, Ashton GH, McGrath JA, Eady RA, Moss C. Thomson MA, et al. Among authors: moss c. Clin Exp Dermatol. 2006 Jan;31(1):45-7. doi: 10.1111/j.1365-2230.2005.01930.x. Clin Exp Dermatol. 2006. PMID: 16309479

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