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Journal of Bioenergetics and Biomembranes|April 1, 1995
Molecular abnormalities of coproporphyrinogen oxidase in patients with hereditary coproporphyriaB Grandchamp, J Lamoril, H PuyDermatology (Basel, Switzerland)|September 19, 2008
Cutaneous aseptic neutrophilic abscesses and Yersinia enterocolitica infection in a case subsequently diagnosed as Crohn's diseaseG Safa, M Loppin, L Tisseau, et al.Revue Neurologique|January 1, 1992
[Neurological, dermatological and biological manifestations of porphyria variegata. A study of 3 families of Italian origin in Marseilles area]R Aquaron, D Lacombe, G C Topi, et al.Journal of Gastroenterology and Hepatology|November 1, 1996
Review: molecular pathogenesis of hepatic acute porphyriasB Grandchamp, H Puy, J Lamoril, et al.Human Heredity|May 1, 1996
Detection of four novel mutations in the porphobilinogen deaminase gene in French Caucasian patients with acute intermittent porphyriaH Puy, J C Deybach, J Lamoril, et al.European Journal of Gastroenterology & Hepatology|February 24, 2001
Amantadine for chronic hepatitis C: pilot study in 14 patientsC Andant, J Lamoril, J C Deybach, et al.Scandinavian Journal of Clinical and Laboratory Investigation|May 1, 1997
Molecular analysis of porphobilinogen (PBG) deaminase gene mutations in acute intermittent porphyria: first study in patients of Slavic originR Rosipal, H Puy, J Lamoril, et al.Cellular and Molecular Biology (Noisy-Le-Grand, France)|February 1, 1997
Acute intermittent porphyria: rapid molecular diagnosisH Puy, R Aquaron, J Lamoril, et al.The British Journal of Dermatology|September 21, 2011
Comprehensive cytochrome P450 CYP1A2 gene analysis in French caucasian patients with familial and sporadic porphyria cutanea tardaD Tchernitchko, A M Robréau, T Lefebvre, 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.Pageof 3