Results 181 to 190 of about 26,198 (235)

HLA-B*58:01 and Risk of Allopurinol-Induced Severe Cutaneous Adverse Reactions in the US.

open access: yesJAMA Dermatol
Campbell CN   +4 more
europepmc   +1 more source

Aqueous and methanol extracts of Paullinia pinnata improve MSUc uptake in macrophages and in vitro antioxidant effects. [PDF]

open access: yesSci Rep
Tseuguem PP   +5 more
europepmc   +1 more source

Allopurinol in Dermatology

open access: yesAmerican Journal of Clinical Dermatology, 2010
Off-label use is common in dermatology, and is inevitable for rare cutaneous diseases such as perforating dermatosis. Allopurinol is traditionally considered to be a drug for hyperuricemia only, but the recent demonstration of its efficacy in congestive heart failure has spurred renewed interest in its application in other clinical specialties.
Tsen-Fang, Tsai, Ting-Yu, Yeh
openaire   +3 more sources

Allopurinol hypersensitivity is primarily mediated by dose-dependent oxypurinol-specific T cell response

open access: yesClinical and Experimental Allergy, 2013
BACKGROUND Allopurinol is a main cause of severe cutaneous adverse reactions (SCAR). How allopurinol induces hypersensitivity remains unknown. Pre-disposing factors are the presence of the HLA-B*58:01 allele, renal failure and possibly the dose taken.
Carlo R Largiadèr, D Yerly
exaly   +2 more sources

Allopurinol and oxypurinol are hydroxyl radical scavengers

open access: yesFEBS Letters, 1987
Allopurinol is a scavenger of the highly reactive hydroxyl radical (k2 approx. 109 M−1s−1). One product of attack of hydroxyl radical upon allopurinol is oxypurinol, which is a major metabolite of allopurinol.
Martin Grootveld, Barry Halliwell
exaly   +2 more sources

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