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Y Nordmann

Showing results (51-60 of 116) with videos related to

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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.
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.
Gastroenterology|June 1, 1987
Porphyria cutanea tarda and HLA-linked hemochromatosis. Evidence against a systematic associationC Beaumont, R Fauchet, L N Phung, 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.
Scandinavian Journal of Gastroenterology|July 1, 1994
A case of association between hepatocellular carcinoma and porphyria variegataJ Germanaud, F Luthier, X Causse, et al.
American Journal of Human Genetics|September 1, 1992
High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyriaX F Gu, F de Rooij, G Voortman, 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 12

Showing results (51-60 of 116) with videos related to

Sort By:
Pageof 12
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.
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.
Gastroenterology|June 1, 1987
Porphyria cutanea tarda and HLA-linked hemochromatosis. Evidence against a systematic associationC Beaumont, R Fauchet, L N Phung, 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.
Scandinavian Journal of Gastroenterology|July 1, 1994
A case of association between hepatocellular carcinoma and porphyria variegataJ Germanaud, F Luthier, X Causse, et al.
American Journal of Human Genetics|September 1, 1992
High frequency of mutations in exon 10 of the porphobilinogen deaminase gene in patients with a CRIM-positive subtype of acute intermittent porphyriaX F Gu, F de Rooij, G Voortman, 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 12