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The British Journal of Dermatology|December 1, 1985
Ultrasound as a screening procedure for methotrexate-induced hepatic damage in severe psoriasisJ A Miller, H Dodd, M H Rustin, et al.
The British Journal of Dermatology|December 1, 1987
The effect of captopril on cutaneous blood flow in patients with primary Raynaud's phenomenonM H Rustin, N E Almond, J A Beacham, et al.
The British Journal of Dermatology|June 25, 2004
Atypical epidermolytic palmoplantar keratoderma presentation associated with a mutation in the keratin 1 geneA Terron-Kwiatkowski, A Terrinoni, B Didona, et al.
The British Journal of Dermatology|December 1, 1990
Silica-associated systemic sclerosis is clinically, serologically and immunologically indistinguishable from idiopathic systemic sclerosisM H Rustin, H A Bull, V Ziegler, et al.
Archives of Disease in Childhood|August 24, 2002
Erythromelalgia: an endothelial disorder responsive to sodium nitroprussideM K H Chan, A T Tucker, S Madden, et al.
The British Journal of Dermatology|April 1, 1994
Neutral lipid storage disease. Case report and lipid studiesM R Judge, D J Atherton, R Salvayre, et al.
Lancet (London, England)|February 4, 1984
Spontaneous remission of multi-system histiocytosis XV Broadbent, J Pritchard, E G Davies, et al.
European Journal of Clinical Pharmacology|January 1, 1984
A double blind trial of UK-38,485, an orally active thromboxane synthetase inhibitor, in the treatment of Raynaud's syndromeM H Rustin, S M Grimes, I B Kovacs, et al.
Archives of Dermatological Research|November 1, 2001
Genomic localization, organization and amplification of the human zinc transporter protein gene, ZNT4, and exclusion as a candidate gene in different clinical variants of acrodermatitis enteropathicaO Bleck, G H Ashton, R Mallipeddi, et al.
The British Journal of Dermatology|March 24, 2000
Laryngeal involvement in the Dowling-Meara variant of epidermolysis bullosa simplex with keratin mutations of severely disruptive potentialC S Shemanko, H M Horn, S G Keohane, et al.
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