Showing results (21-30 of 87) with videos related to
Sort By:
Pageof 9
Journal of Inherited Metabolic Disease|January 1, 1990
Coexistent hereditary coproporphyria and congenital erythropoietic porphyria (Günther disease)Y Nordmann, D Amram, J C Deybach, et al.Pediatric Radiology|January 1, 1988
Radiological features in congenital erythropoietic porphyria (Gunther's disease). Report of 3 casesM Levesque, P Legmann, A Le Cloirec, et al.Annales De Dermatologie Et De Venereologie|October 12, 2010
[Porphyria cutanea tarda in a child undergoing bone marrow grafting]M Royer-Bégyn, P Teira, 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.Biochemical Pharmacology|March 15, 1983
Study of anaesthetic agents for their ability to elicit porphyrin biosynthesis in chick embryo liverH de Verneuil, J C Deybach, N Phung, et al.Life Sciences|January 1, 1993
Decreased nocturnal plasma melatonin levels in patients with recurrent acute intermittent porphyria attacksH Puy, J C Deybach, P Baudry, et al.Journal of Internal Medicine|July 3, 2009
Role of two nutritional hepatic markers (insulin-like growth factor 1 and transthyretin) in the clinical assessment and follow-up of acute intermittent porphyria patientsC Delaby, J To-Figueras, J C Deybach, 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.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.Pageof 9