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M O Doss

Showing results (61-70 of 74) with videos related to

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Zeitschrift Fur Gastroenterologie|April 1, 1993
[Cimetidine in treatment of acute intermittent porphyria]M Siepmann, U Stölzel, I Sieg, et al.
Clinical Chemistry|September 11, 1998
5-Aminolevulinic acid dehydratase deficiency porphyria: a twenty-year clinical and biochemical follow-upU Gross, S Sassa, K Jacob, et al.
Zeitschrift Fur Gastroenterologie|February 1, 1993
[Porphyrin-induced biliary cirrhosis in protoporphyria: indications for liver transplantation]T Steinmüller, M Frank, R Kretschmar, et al.
Liver|June 1, 1996
Liver failure in erythropoietic protoporphyria associated with choledocholithiasis and severe post-transplantation polyneuropathyG Lock, A Holstege, A R Mueller, et al.
Molecular and Cellular Probes|February 5, 2000
New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyriaU Gross, H Puy, M Doss, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
A molecular, enzymatic and clinical study in a family with hereditary coproporphyriaU Gross, H Puy, U Meissauer, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
The third case of Doss porphyria (delta-amino-levulinic acid dehydratase deficiency) in GermanyM O Doss, T Stauch, U Gross, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 4, 2002
Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyriaU Gross, H Puy, A Kühnel, et al.
Deutsche Medizinische Wochenschrift (1946)|July 10, 1992
[Liver transplantation in erythrohepatic protoporphyria]T Steinmüller, M O Doss, R Steffen, et al.
Molecular Microbiology|October 10, 1998
Regulation of Pseudomonas aeruginosa hemF and hemN by the dual action of the redox response regulators Anr and DnrA Rompf, C Hungerer, T Hoffmann, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Zeitschrift Fur Gastroenterologie|April 1, 1993
[Cimetidine in treatment of acute intermittent porphyria]M Siepmann, U Stölzel, I Sieg, et al.
Clinical Chemistry|September 11, 1998
5-Aminolevulinic acid dehydratase deficiency porphyria: a twenty-year clinical and biochemical follow-upU Gross, S Sassa, K Jacob, et al.
Zeitschrift Fur Gastroenterologie|February 1, 1993
[Porphyrin-induced biliary cirrhosis in protoporphyria: indications for liver transplantation]T Steinmüller, M Frank, R Kretschmar, et al.
Liver|June 1, 1996
Liver failure in erythropoietic protoporphyria associated with choledocholithiasis and severe post-transplantation polyneuropathyG Lock, A Holstege, A R Mueller, et al.
Molecular and Cellular Probes|February 5, 2000
New mutations of the hydroxymethylbilane synthase gene in German patients with acute intermittent porphyriaU Gross, H Puy, M Doss, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
A molecular, enzymatic and clinical study in a family with hereditary coproporphyriaU Gross, H Puy, U Meissauer, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
The third case of Doss porphyria (delta-amino-levulinic acid dehydratase deficiency) in GermanyM O Doss, T Stauch, U Gross, et al.
Cellular and Molecular Biology (Noisy-Le-Grand, France)|April 4, 2002
Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyriaU Gross, H Puy, A Kühnel, et al.
Deutsche Medizinische Wochenschrift (1946)|July 10, 1992
[Liver transplantation in erythrohepatic protoporphyria]T Steinmüller, M O Doss, R Steffen, et al.
Molecular Microbiology|October 10, 1998
Regulation of Pseudomonas aeruginosa hemF and hemN by the dual action of the redox response regulators Anr and DnrA Rompf, C Hungerer, T Hoffmann, et al.
Pageof 8