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Blood|March 7, 1998
Neonatal hemolytic anemia due to inherited harderoporphyria: clinical characteristics and molecular basisJ Lamoril, H Puy, L Gouya, et al.Human Mutation|January 15, 1999
Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation updateR Rosipal, J Lamoril, H Puy, et al.Human Molecular Genetics|November 13, 1998
Molecular characterization of homozygous variegate porphyriaA G Roberts, H Puy, T A Dailey, et al.European Journal of Biochemistry|April 2, 1999
Heme and acute inflammation role in vivo of heme in the hepatic expression of positive acute-phase reactants in ratsS Lyoumi, H Puy, F Tamion, et al.The British Journal of Dermatology|July 19, 2012
A management algorithm for congenital erythropoietic porphyria derived from a study of 29 casesR P Katugampola, A V Anstey, A Y Finlay, et al.The British Journal of Dermatology|July 24, 2012
Congenital erythropoietic porphyria: a single-observer clinical study of 29 casesR P Katugampola, M N Badminton, A Y Finlay, et al.Journal of Internal Medicine|March 3, 2018
Recurrent attacks of acute hepatic porphyria: major role of the chronic inflammatory response in the liverC Schmitt, H Lenglet, A Yu, et al.Pageof 9