Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J C Deybach

Showing results (31-40 of 112) with videos related to

Pageof 12
Sort By:
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 14, 1995
Variegate porphyria: diagnostic value of fluorometric scanning of plasma porphyrinsV Da Silva, S Simonin, J C Deybach, et al.
Current Problems in Dermatology|January 1, 1991
Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Günther's disease)Y Nordmann, J C Deybach, H de Verneuil, 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.
Biochimica Et Biophysica Acta|May 22, 1980
Studies of porphyrin synthesis in fibroblasts of patients with congenital erythropoietic porphyria and one patient with homozygous coproporphyriaB Grandchamp, J C Deybach, M Grelier, et al.
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.
Pageof 12

Showing results (31-40 of 112) with videos related to

Sort By:
Pageof 12
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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 14, 1995
Variegate porphyria: diagnostic value of fluorometric scanning of plasma porphyrinsV Da Silva, S Simonin, J C Deybach, et al.
Current Problems in Dermatology|January 1, 1991
Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Günther's disease)Y Nordmann, J C Deybach, H de Verneuil, 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.
Biochimica Et Biophysica Acta|May 22, 1980
Studies of porphyrin synthesis in fibroblasts of patients with congenital erythropoietic porphyria and one patient with homozygous coproporphyriaB Grandchamp, J C Deybach, M Grelier, et al.
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.
Pageof 12