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Clinical and Experimental Dermatology|October 18, 2013
X-linked dominant protoporphyria: a new porphyriaM J Seager, S D Whatley, A V Anstey, et al.
Photodermatology, Photoimmunology & Photomedicine|May 26, 2007
Rate of acute adverse events for narrow-band UVB and Psoralen-UVA phototherapyJ A Martin, S Laube, C Edwards, et al.
The British Journal of Dermatology|May 15, 2008
Serum 25-hydroxyvitamin D in erythropoietic protoporphyriaS A Holme, A V Anstey, M N Badminton, et al.
Clinical and Experimental Dermatology|May 24, 2008
Sclerodermatous changes of face, neck and scalp associated with familial porphyria cutanea tardaC L Thomas, M N Badminton, J R S Rendall, et al.
QJM : Monthly Journal of the Association of Physicians|July 4, 2002
Erythrocyte thiopurine methyl transferase assessment prior to azathioprine use in the UKS A Holme, J A Duley, J Sanderson, et al.
Mutation Research|March 1, 1992
A comparison of the response of unstimulated and stimulated T-lymphocytes and fibroblasts from normal, xeroderma pigmentosum and trichothiodystrophy donors to the lethal action of UV-CC F Arlett, S A Harcourt, J Cole, et al.
The British Journal of Dermatology|August 17, 2006
Erythropoietic protoporphyria in the U.K.: clinical features and effect on quality of lifeS A Holme, A V Anstey, A Y Finlay, et al.
The British Journal of Dermatology|April 26, 2006
Modulation of ultraviolet (UV) transmission by emollients: relevance to narrowband UVB phototherapy and psoralen plus UVA photochemotherapyS G H Otman, C Edwards, A D Pearse, et al.
The British Journal of Dermatology|October 3, 2017
How to write a Critically Appraised Topic: evidence to underpin routine clinical practiceJ Callander, A V Anstey, J R Ingram, et al.
The British Journal of Dermatology|September 27, 2005
Photosensitive Smith-Lemli-Opitz syndrome is not caused by a single gene mutation: analysis of the gene encoding 7-dehydrocholesterol reductase in five U.K. familiesA V Anstey, R M Azurdia, L E Rhodes, et al.
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