Darryl C. DeVivo

Affiliations: 
Columbia University, New York, NY 
Area:
Neurochemistry, mitochondrial disorders, neuromuscular transmission
Website:
http://www.giblinlab.org/index.html
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"Darryl DeVivo"
Mean distance: 13.51 (cluster 6)
 
SNBCP
Cross-listing: Neurotree

Parents

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Raymond D. Adams post-doc 1966-1967 MGH (Neurotree)
Philip Rodgers Dodge post-doc 1969-1970 Washington University School of Medicine (Neurotree)

Children

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A M. Barrett grad student 1992-1995 Kessler Foundation (Neurotree)
Michael M. Segal post-doc 1984-1987 Columbia University Medical School (Neurotree)
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Publications

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Mattiazzi M, Vijayvergiya C, Gajewski CD, et al. (2004) The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants. Human Molecular Genetics. 13: 869-79
DiMauro S, Hirano M, Kaufmann P, et al. (2002) Clinical features and genetics of myoclonic epilepsy with ragged red fibers. Advances in Neurology. 89: 217-29
DeVivo DC. (2002) Effect of L-carnitine treatment for valproate-induced hepatotoxicity. Neurology. 58: 507-8
Vázquez-Memije ME, Shanske S, Santorelli FM, et al. (1998) Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutations. Journal of Inherited Metabolic Disease. 21: 829-36
Vu TH, Sciacco M, Tanji K, et al. (1998) Clinical manifestations of mitochondrial DNA depletion. Neurology. 50: 1783-90
Handran SD, Werth JL, DeVivo DC, et al. (1997) Mitochondrial morphology and intracellular calcium homeostasis in cytochrome oxidase-deficient human fibroblasts. Neurobiology of Disease. 3: 287-98
Vazquez-Memije ME, Shanske S, Santorelli FM, et al. (1996) Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome. Journal of Inherited Metabolic Disease. 19: 43-50
Tager JM, Moser HW, Barker PB, et al. (1996) The MRI suggests a leukodystrophy, but tests are negative - What should we do? Probing white-matter disorders Molecular and Chemical Neuropathology. 27: 1-106
Moudy AM, Handran SD, Goldberg MP, et al. (1995) Abnormal calcium homeostasis and mitochondrial polarization in a human encephalomyopathy. Proceedings of the National Academy of Sciences of the United States of America. 92: 729-33
Tawil R, Ptacek LJ, Pavlakis SG, et al. (1994) Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features. Annals of Neurology. 35: 326-30
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