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D C Devivo

Showing results (51-60 of 75) with videos related to

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Archives of Neurology|June 1, 1970
Familial adult-onset proximal spinal muscular atrophy. Report of a family with type II hyperlipoproteinemiaS H Quarfordt, D C DeVivo, W K Engel, et al.
Muscle & Nerve|March 1, 1978
Biochemical and physiologic consequences of carnitine palmityltransferase deficiencyJ E Carroll, M H Brooke, D C DeVivo, et al.
Neurology|June 1, 1977
Coxsackie A9 focal encephalitis associated with acute infantile hemiplegia and porencephalyE G Chalhub, D C Devivo, B A Siegel, et al.
Metabolism: Clinical and Experimental|June 1, 1979
Fasting as a provocative test in neuromuscular diseasesJ E Carroll, D C DeVivo, M H Brooke, et al.
Annals of Neurology|December 1, 1979
Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (Leigh disease)D C DeVivo, M W Haymond, K A Obert, et al.
The Journal of Pediatrics|January 1, 1981
Reye syndrome complicated by a generalized herpes simplex type I infectionE G Chalhub, D C DeVivo, J P Keating, et al.
Stroke|January 1, 1991
Middle cerebral artery blood velocity and cerebral blood flow in sickle cell diseaseL M Brass, I Prohovnik, S G Pavlakis, et al.
Cancer|February 1, 1974
Proceedings: Parenchymatous degeneration of the central nervous system in childhood leukemiaB Hendin, D C DeVivo, R Torack, et al.
Transactions of the American Neurological Association|January 1, 1981
Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiencyS DiMauro, J F Nicholson, A P Hays, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutationsM E Vázquez-Memije, S Shanske, F M Santorelli, et al.
Pageof 8

Showing results (51-60 of 75) with videos related to

Sort By:
Pageof 8
Archives of Neurology|June 1, 1970
Familial adult-onset proximal spinal muscular atrophy. Report of a family with type II hyperlipoproteinemiaS H Quarfordt, D C DeVivo, W K Engel, et al.
Muscle & Nerve|March 1, 1978
Biochemical and physiologic consequences of carnitine palmityltransferase deficiencyJ E Carroll, M H Brooke, D C DeVivo, et al.
Neurology|June 1, 1977
Coxsackie A9 focal encephalitis associated with acute infantile hemiplegia and porencephalyE G Chalhub, D C Devivo, B A Siegel, et al.
Metabolism: Clinical and Experimental|June 1, 1979
Fasting as a provocative test in neuromuscular diseasesJ E Carroll, D C DeVivo, M H Brooke, et al.
Annals of Neurology|December 1, 1979
Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (Leigh disease)D C DeVivo, M W Haymond, K A Obert, et al.
The Journal of Pediatrics|January 1, 1981
Reye syndrome complicated by a generalized herpes simplex type I infectionE G Chalhub, D C DeVivo, J P Keating, et al.
Stroke|January 1, 1991
Middle cerebral artery blood velocity and cerebral blood flow in sickle cell diseaseL M Brass, I Prohovnik, S G Pavlakis, et al.
Cancer|February 1, 1974
Proceedings: Parenchymatous degeneration of the central nervous system in childhood leukemiaB Hendin, D C DeVivo, R Torack, et al.
Transactions of the American Neurological Association|January 1, 1981
Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiencyS DiMauro, J F Nicholson, A P Hays, et al.
Journal of Inherited Metabolic Disease|December 31, 1998
Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutationsM E Vázquez-Memije, S Shanske, F M Santorelli, et al.
Pageof 8