Moss C - Search Results

1

Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragility.

Has C, Bauer JW, Bodemer C, Bolling MC, Bruckner-Tuderman L, Diem A, Fine JD, Heagerty A, Hovnanian A, Marinkovich MP, Martinez AE, McGrath JA, Moss C, Murrell DF, Palisson F, Schwieger-Briel A, Sprecher E, Tamai K, Uitto J, Woodley DT, Zambruno G, Mellerio JE. Has C, et al. Among authors: moss c. Br J Dermatol. 2020 Oct;183(4):614-627. doi: 10.1111/bjd.18921. Epub 2020 Mar 11. Br J Dermatol. 2020. PMID: 32017015 Review.

2

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

3

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

4

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.

5

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

6

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

7

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.

8

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

9

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

10

Allogeneic bone marrow transplantation in a 7-year-old girl with congenital erythropoietic porphyria: a treatment dilemma.

Taibjee SM, Stevenson OE, Abdullah A, Tan CY, Darbyshire P, Moss C, Goodyear H, Heagerty A, Whatley S, Badminton MN. Taibjee SM, et al. Among authors: moss c. Br J Dermatol. 2007 Mar;156(3):567-71. doi: 10.1111/j.1365-2133.2006.07699.x. Br J Dermatol. 2007. PMID: 17300251

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