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Journal of Inherited Metabolic Disease|April 8, 2006
Biochemical compared to molecular diagnosis in acute intermittent porphyriaU Grob, H Puy, K Jacob, et al.La Revue De Medecine Interne|January 1, 1994
[Hepatic porphyria: diagnostic and therapeutic strategies]D Vincent, J F Devars du Mayne, J C Deybach, et al.European Journal of Pediatrics|October 20, 2000
New insights into the pathogenesis of erythropoietic protoporphyria and their impact on patient careX Schneider-Yin, L Gouya, A Meier-Weinand, et al.Biochemical and Biophysical Research Communications|December 16, 1991
Human erythropoietic protoporphyria: two point mutations in the ferrochelatase geneJ Lamoril, S Boulechfar, H de Verneuil, et al.Human Molecular Genetics|February 1, 1995
A molecular defect in coproporphyrinogen oxidase gene causing harderoporphyria, a variant form of hereditary coproporphyriaJ Lamoril, P Martasek, J C Deybach, et al.American Journal of Human Genetics|May 1, 1984
Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyriaH de Verneuil, C Beaumont, J C Deybach, et al.Presse Medicale (Paris, France : 1983)|January 24, 1987
[Drug risk of hepatic porphyria. Development of an animal experiment model]J C Deybach, V Da Silva, L N Phung, et al.The Journal of Laboratory and Clinical Medicine|April 1, 1981
Congenital erythropoietic porphyria (Günther's disease): enzymatic studies on two cases of late onsetJ C Deybach, H de Verneuil, N Phung, et al.Blood|August 15, 2000
Mutations in the iron-sulfur cluster ligands of the human ferrochelatase lead to erythropoietic protoporphyriaX Schneider-Yin, L Gouya, M Dorsey, et al.Human Genetics|January 1, 1992
Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyriaS Boulechfar, V Da Silva, J C Deybach, et al.Pageof 9