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D A Stumpf

Showing results (31-40 of 42) with videos related to

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Biochemical Medicine|April 1, 1979
Loosely coupled mitochondrial oxidative phosphorylation induced by protoporphyrinD A Stumpf, E R McCabe, J K Parks, et al.
Biochemical Medicine|April 1, 1982
A mechanism of toxicity of isovaleric acid in rat liver mitochondriaB J Bergen, D A Stumpf, R Haas, et al.
Muscle & Nerve|January 1, 1982
Protonmotive force in muscle mitochondriaD A Stumpf, R Haas, L A Eguren, et al.
Neurology|November 1, 1984
Brain mitochondrial metabolism in experimental thiamine deficiencyW D Parker, R Haas, D A Stumpf, et al.
Neurology|April 1, 1976
Malignant atrophic papulosis (Kohlmeier-Degos disease) in childhoodF A Horner, G J Myers, D A Stumpf, et al.
Neurology|January 1, 1987
Friedreich's disease: V. Variant form with vitamin E deficiency and normal fat absorptionD A Stumpf, R Sokol, D Bettis, et al.
The Journal of Pediatrics|January 1, 1984
Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acidR Matalon, D A Stumpf, K Michals, et al.
The Journal of Pediatrics|June 1, 1982
Glutaric acidemia type II: clinical, biochemical, and morphologic considerationsS I Goodman, D O Stene, E R McCabe, et al.
The Journal of Laboratory and Clinical Medicine|May 1, 1988
Isolated vitamin E deficiency in the absence of fat malabsorption--familial and sporadic cases: characterization and investigation of causesR J Sokol, H J Kayden, D B Bettis, et al.
Annals of Neurology|March 1, 1996
Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiencyA Hentati, H X Deng, W Y Hung, et al.
Pageof 5

Showing results (31-40 of 42) with videos related to

Sort By:
Pageof 5
Biochemical Medicine|April 1, 1979
Loosely coupled mitochondrial oxidative phosphorylation induced by protoporphyrinD A Stumpf, E R McCabe, J K Parks, et al.
Biochemical Medicine|April 1, 1982
A mechanism of toxicity of isovaleric acid in rat liver mitochondriaB J Bergen, D A Stumpf, R Haas, et al.
Muscle & Nerve|January 1, 1982
Protonmotive force in muscle mitochondriaD A Stumpf, R Haas, L A Eguren, et al.
Neurology|November 1, 1984
Brain mitochondrial metabolism in experimental thiamine deficiencyW D Parker, R Haas, D A Stumpf, et al.
Neurology|April 1, 1976
Malignant atrophic papulosis (Kohlmeier-Degos disease) in childhoodF A Horner, G J Myers, D A Stumpf, et al.
Neurology|January 1, 1987
Friedreich's disease: V. Variant form with vitamin E deficiency and normal fat absorptionD A Stumpf, R Sokol, D Bettis, et al.
The Journal of Pediatrics|January 1, 1984
Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acidR Matalon, D A Stumpf, K Michals, et al.
The Journal of Pediatrics|June 1, 1982
Glutaric acidemia type II: clinical, biochemical, and morphologic considerationsS I Goodman, D O Stene, E R McCabe, et al.
The Journal of Laboratory and Clinical Medicine|May 1, 1988
Isolated vitamin E deficiency in the absence of fat malabsorption--familial and sporadic cases: characterization and investigation of causesR J Sokol, H J Kayden, D B Bettis, et al.
Annals of Neurology|March 1, 1996
Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiencyA Hentati, H X Deng, W Y Hung, et al.
Pageof 5