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Pathologie-Biologie|September 21, 2010
[Inheritance in erythropoietic protoporphyria]C Schmitt, S Ducamp, L Gouya, et al.Cellular and Molecular Biology (Noisy-Le-Grand, France)|March 10, 2009
Excessive erythrocyte PPIX influences the hematologic status and iron metabolism in patients with dominant erythropoietic protoporphyriaC Delaby, S Lyoumi, S Ducamp, et al.La Revue De Medecine Interne|January 18, 2016
[Porphyrias and haem related disorders]K Peoc'h, C Martin-Schmitt, N Talbi, et al.Journal of Bioenergetics and Biomembranes|April 1, 1995
Porphobilinogen deaminase gene structure and molecular defectsJ C Deybach, H PuyBlood|March 9, 1999
Inheritance in erythropoietic protoporphyria: a common wild-type ferrochelatase allelic variant with low expression accounts for clinical manifestationL Gouya, H Puy, J Lamoril, et al.Cellular and Molecular Biology (Noisy-Le-Grand, France)|August 7, 2009
The molecular genetics of erythropoietic protoporphyriaG H Elder, L Gouya, S D Whatley, et al.American Journal of Human Genetics|June 1, 1997
Molecular epidemiology and diagnosis of PBG deaminase gene defects in acute intermittent porphyriaH Puy, J C Deybach, J Lamoril, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|March 4, 1999
Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresisD Tchernitchko, J Lamoril, H Puy, et al.The Journal of Investigative Dermatology|September 18, 1998
Mutations in the ferrochelatase gene of four Spanish patients with erythropoietic protoporphyriaL Gouya, X Schneider-Yin, U Rüfenacht, et al.Pageof 144