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Darryl C. DeVivo - Publications

Affiliations: 
Columbia University, New York, NY 
Area:
Neurochemistry, mitochondrial disorders, neuromuscular transmission
Website:
http://www.giblinlab.org/index.html

89 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2010 Stratigopoulos G, Lanzano P, Deng L, Guo J, Kaufmann P, Darras B, Finkel R, Tawil R, McDermott MP, Martens W, Devivo DC, Chung WK. Association of plastin 3 expression with disease severity in spinal muscular atrophy only in postpubertal females. Archives of Neurology. 67: 1252-6. PMID 20937953 DOI: 10.1001/archneurol.2010.239  0.68
2004 Mattiazzi M, Vijayvergiya C, Gajewski CD, DeVivo DC, Lenaz G, Wiedmann M, Manfredi G. The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants. Human Molecular Genetics. 13: 869-79. PMID 14998933 DOI: 10.1093/hmg/ddh103  1
2002 DiMauro S, Hirano M, Kaufmann P, Tanji K, Sano M, Shungu DC, Bonilla E, DeVivo DC. Clinical features and genetics of myoclonic epilepsy with ragged red fibers. Advances in Neurology. 89: 217-29. PMID 11968448  1
2002 DeVivo DC. Effect of L-carnitine treatment for valproate-induced hepatotoxicity. Neurology. 58: 507-8. PMID 11839873  1
1998 Vázquez-Memije ME, Shanske S, Santorelli FM, Kranz-Eble P, DeVivo DC, DiMauro S. 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. PMID 9870208 DOI: 10.1023/A:1005418718299  1
1998 Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Clinical manifestations of mitochondrial DNA depletion. Neurology. 50: 1783-90. PMID 9633728  1
1998 Arnon R, Devivo D, Defelice AR, Kazlow PG. Acute hepatic failure in a child treated with lamotrigine Pediatric Neurology. 18: 251-252. PMID 9568923 DOI: 10.1016/S0887-8994(97)00196-3  1
1997 Handran SD, Werth JL, DeVivo DC, Rothman SM. Mitochondrial morphology and intracellular calcium homeostasis in cytochrome oxidase-deficient human fibroblasts. Neurobiology of Disease. 3: 287-98. PMID 9173926 DOI: 10.1006/nbdi.1996.0125  1
1996 Vazquez-Memije ME, Shanske S, Santorelli FM, Kranz-Eble P, Davidson E, DeVivo DC, DiMauro S. Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome. Journal of Inherited Metabolic Disease. 19: 43-50. PMID 8830176 DOI: 10.1007/BF01799347  1
1996 Tager JM, Moser HW, Barker PB, Barth PG, Boltshauser E, Campagnoni AT, Dawson G, DeVivo DC, Federico A, Fluharty AL, Gieselmann V, Hodes ME, Hurko O, Jaeken J, Kruse B, et al. The MRI suggests a leukodystrophy, but tests are negative - What should we do? Probing white-matter disorders Molecular and Chemical Neuropathology. 27: 1-106. PMID 8790669  1
1995 Moudy AM, Handran SD, Goldberg MP, Ruffin N, Karl I, Kranz-Eble P, DeVivo DC, Rothman SM. 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. PMID 7846043 DOI: 10.1073/pnas.92.3.729  1
1994 Lasser DM, DeVivo DC, Garvin J, Wilhelmsen KC. Turcot's syndrome: evidence for linkage to the adenomatous polyposis coli (APC) locus. Neurology. 44: 1083-6. PMID 8208405  0.68
1994 Tawil R, Ptacek LJ, Pavlakis SG, DeVivo DC, Penn AS, Ozdemir C, Griggs RC. Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features. Annals of Neurology. 35: 326-30. PMID 8080508 DOI: 10.1002/ana.410350313  1
1994 Danpure CJ, Fryer P, Griffiths S, Guttridge KM, Jennings PR, Allsop J, Moser AB, Naidu S, Moser HW, MacCollin M. Cytosolic compartmentalization of hepatic alanine:glyoxylate aminotransferase in patients with aberrant peroxisomal biogenesis and its effect on oxalate metabolism. Journal of Inherited Metabolic Disease. 17: 27-40. PMID 8051936 DOI: 10.1007/BF00735393  1
1993 Santorelli FM, Shanske S, Macaya A, DeVivo DC, DiMauro S. The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome. Annals of Neurology. 34: 827-34. PMID 8250532 DOI: 10.1002/ana.410340612  1
1992 Ciafaloni E, Ricci E, Shanske S, Moraes CT, Silvestri G, Hirano M, Simonetti S, Angelini C, Donati MA, Garcia C, Martinuzzi A, Mosewich R, Servidei S, Zammarchi E, Bonilla E, ... DeVivo DC, et al. MELAS: Clinical features, biochemistry, and molecular genetics Annals of Neurology. 31: 391-398. PMID 1586140 DOI: 10.1002/ana.410310408  1
1992 Hirano M, Ricci E, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, DiMauro S, Rowland LP. Melas: an original case and clinical criteria for diagnosis. Neuromuscular Disorders : Nmd. 2: 125-35. PMID 1422200 DOI: 10.1016/0960-8966(92)90045-8  1
1991 Brass LM, Prohovnik I, Pavlakis SG, DeVivo DC, Piomelli S, Mohr JP. Middle cerebral artery blood velocity and cerebral blood flow in sickle cell disease. Stroke; a Journal of Cerebral Circulation. 22: 27-30. PMID 1987669  0.68
1991 Rowland LP, Blake DM, Hirano M, Di Mauro S, Schon EA, Hays AP, Devivo DC. Clinical syndromes associated with ragged red fibers. Revue Neurologique. 147: 467-73. PMID 1962052  1
1991 Lombes A, Nakase H, Tritschler HJ, Kadenbach B, Bonilla E, DeVivo DC, Schon EA, DiMauro S. Biochemical and molecular analysis of cytochrome c oxidase deficiency in Leigh's syndrome. Neurology. 41: 491-8. PMID 1849240  0.68
1991 DiMauro S, Ricci E, Hirano M, DeVivo DC. Epilepsy in mitochondrial encephalomyopathies. Epilepsy Research. Supplement. 4: 173-80. PMID 1815599  1
1990 Gibson KM, Aramaki S, Sweetman L, Nyhan WL, DeVivo DC, Hodson AK, Jakobs C. Stable isotope dilution analysis of 4-hydroxybutyric acid: an accurate method for quantification in physiological fluids and the prenatal diagnosis of 4-hydroxybutyric aciduria. Biomedical & Environmental Mass Spectrometry. 19: 89-93. PMID 2407302  1
1990 Tein I, DiMauro S, DeVivo DC. Recurrent childhood myoglobinuria. Advances in Pediatrics. 37: 77-117. PMID 2264536  1
1990 DiMauro S, Lombes A, Nakase H, Mita S, Fabrizi GM, Tritschler HJ, Bonilla E, Miranda AF, DeVivo DC, Schon EA. Cytochrome c oxidase deficiency. Pediatric Research. 28: 536-41. PMID 2175026 DOI: 10.1203/00006450-199011000-00025  0.68
1990 Medina L, Chi TL, DeVivo DC, Hilal SK. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect. Ajr. American Journal of Roentgenology. 154: 1269-74. PMID 2159689 DOI: 10.2214/ajr.154.6.2159689  1
1990 Medina L, Chi TL, DeVivo DC, Hilal SK. MR findings in patients with subacute necrotizing encephalomyelopathy (Leigh syndrome): correlation with biochemical defect. Ajnr. American Journal of Neuroradiology. 11: 379-84. PMID 2156413  1
1989 Friedman HS, Schold SC, Mahaley MS, Colvin OM, Oakes WJ, Vick NA, Burger PC, Bigner SH, Borowitz M, Halperin EC. Phase II treatment of medulloblastoma and pineoblastoma with melphalan: clinical therapy based on experimental models of human medulloblastoma. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 7: 904-11. PMID 2738624  1
1989 Pavlakis SG, Prohovnik I, Piomelli S, DeVivo DC. Neurologic complications of sickle cell disease. Advances in Pediatrics. 36: 247-76. PMID 2675570  1
1989 Zeviani M, Bonilla E, DeVivo DC, DiMauro S. Mitochondrial diseases. Neurologic Clinics. 7: 123-56. PMID 2646519  1
1989 Gibson KM, DeVivo DC, Jakobs C. Vigabatrin therapy in patient with succinic semialdehyde dehydrogenase deficiency. Lancet. 2: 1105-6. PMID 2572834 DOI: 10.1016/S0140-6736(89)91126-4  0.68
1989 Moraes CT, DiMauro S, Zeviani M, Lombes A, Shanske S, Miranda AF, Nakase H, Bonilla E, Werneck LC, Servidei S, Nonaka I, Koga Y, Spiro AJ, Brownell AKW, Schmidt B, ... ... DeVivo DC, et al. Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearne-Sayre syndrome New England Journal of Medicine. 320: 1293-1299. PMID 2541333 DOI: 10.1056/NEJM198905183202001  1
1988 Velázquez A, DeCéspedes C, DeVivo DC, Costin G, Shaw KN. Hepatic metabolites and uric acid excretion in fructose-1,6-diphosphatase deficiency. Journal of Inherited Metabolic Disease. 11: 303-4. PMID 3148073 DOI: 10.1007/BF01800375  1
1988 Reichmann H, Maltese WA, DeVivo DC. Enzymes of fatty acid beta-oxidation in developing brain. Journal of Neurochemistry. 51: 339-44. PMID 2899130 DOI: 10.1111/j.1471-4159.1988.tb01044.x  1
1988 DeVivo DC. Treatment of Reye's syndrome: Consensus and controversy Round Table Series - Royal Society of Medicine. 133-155.  1
1987 DiMauro S, Bonilla E, Zeviani M, Servidei S, DeVivo DC, Schon EA. Mitochondrial myopathies. Journal of Inherited Metabolic Disease. 10: 113-28. PMID 2824920 DOI: 10.1007/BF01812852  1
1985 DiMauro S, Bonilla E, Zeviani M, Nakagawa M, DeVivo DC. Mitochondrial myopathies. Annals of Neurology. 17: 521-38. PMID 3927817 DOI: 10.1002/ana.410170602  0.68
1985 Trevisan CP, Reichmann H, DeVivo DC, DiMauro S. Beta-oxidation enzymes in normal human muscle and in muscle from a patient with an unusual form of myopathic carnitine deficiency. Muscle & Nerve. 8: 672-5. PMID 2932640 DOI: 10.1002/mus.880080809  1
1983 Haymond MW, Howard C, Ben-Galim E, DeVivo DC. Effects of ketosis on glucose flux in children and adults. The American Journal of Physiology. 245: E373-8. PMID 6353936  1
1983 DiMauro S, Nicholson JF, Hays AP, Eastwood AB, Papadimitriou A, Koenigsberger R, DeVivo DC. Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency. Annals of Neurology. 14: 226-34. PMID 6312869 DOI: 10.1002/ana.410140209  0.68
1981 Chalhub EG, DeVivo DC, Keating JP, Haymond MW, Feigin RD. Reye syndrome complicated by a generalized herpes simplex type I infection. The Journal of Pediatrics. 98: 73-6. PMID 7452408 DOI: 10.1016/S0022-3476(81)80540-9  1
1981 DiMauro S, Nicholson JF, Hays AP, Eastwood AB, Koenigsberger R, DeVivo DC. Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency. Transactions of the American Neurological Association. 106: 205-7. PMID 6294949  1
1981 Mandelbaum DE, Hall WW, Paneth N, Wolff RR, DeVivo DC. SSPE, measles virus, and the matrix protein: report of a case with unusual immunochemical findings. Annals of Neurology. 10: 351-4. PMID 6172078 DOI: 10.1002/ana.410100406  0.68
1980 Carroll JE, Brooke MH, DeVivo DC, Shumate JB, Kratz R, Ringel SP, Hagberg JM. Carnitine "deficiency": lack of response to carnitine therapy. Neurology. 30: 618-26. PMID 7189838 DOI: 10.1212/WNL.30.6.618  0.68
1980 DeVivo DC. Major clinical aspects of Reye's syndrome University of Michigan Medical Center Journal. 46: 2-3.  1
1980 Huttenlocher PR, DeVivo DC. Workshop C: How can health planning provide appropriate access to emergency care for the patient with Reye's syndrome? University of Michigan Medical Center Journal. 46: 17.  1
1979 Mantovani J, DeVivo DC. Effects of taurine on seizures and growth hormone release in epileptic patients. Archives of Neurology. 36: 672-4. PMID 508122 DOI: 10.1001/archneur.1979.00500470042006  0.68
1979 Carroll JE, DeVivo DC, Brooke MH, Planer GJ, Hagberg JH. Fasting as a provocative test in neuromuscular diseases. Metabolism: Clinical and Experimental. 28: 683-7. PMID 449706 DOI: 10.1016/0026-0495(79)90023-4  1
1979 Rothman SM, Nelson JS, DeVivo DC, Coxe WS. Congenital astrocytoma presenting with intracerebral hematoma. Case report. Journal of Neurosurgery. 51: 237-9. PMID 448433 DOI: 10.3171/jns.1979.51.2.0237  1
1979 DeVivo DC, Haymond MW, Obert KA, Nelson JS, Pagliara AS. Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (Leigh disease). Annals of Neurology. 6: 483-94. PMID 119480 DOI: 10.1002/ana.410060605  1
1979 Hahn TJ, Halstead LR, DeVivo DC. Disordered mineral metabolism produced by ketogenic diet therapy. Calcified Tissue International. 28: 17-22. PMID 115548 DOI: 10.1007/BF02441213  1
1979 Taysi K, Devivo DC, Sekhon GS. Partial trisomy 15 and intractable seizures. Acta Paediatrica Scandinavica. 68: 445-7. PMID 108917  1
1978 Carroll JE, Brooke MH, DeVivo DC, Kaiser KK, Hagberg JM. Biochemical and physiologic consequences of carnitine palmityltransferase deficiency. Muscle & Nerve. 1: 103-10. PMID 750917 DOI: 10.1002/mus.880010203  1
1978 DeVivo DC, Leckie MP, Ferrendelli JS, McDougal DB. Chronic ketosis and cerebral metabolism. Annals of Neurology. 3: 331-37. PMID 666275 DOI: 10.1002/ana.410030410  1
1978 Haymond MW, Karl IE, Keating JP, DeVivo DC. Metabolic response to hypertonic glucose administration in Reye syndrome. Annals of Neurology. 3: 207-15. PMID 666261 DOI: 10.1002/ana.410030305  1
1978 Haymond MW, Strobel KE, DeVivo DC. Muscle wasting and carbohydrate homeostasis in Duchenne muscular dystrophy. Neurology. 28: 1224-31. PMID 569782  0.68
1978 Hillman RE, Berg L, DeVivo DC. Valproic acid (dipropylacetic acid) - an inhibitor of branched chain fatty acid dehydrogenase Pediatric Research. 12: No.861.  1
1977 DeVivo DC, Haymond MW, Leckie MP, Bussman YL, McDougal DB, Pagliara AS. The clinical and biochemical implications of pyruvate carboxylase deficiency. The Journal of Clinical Endocrinology and Metabolism. 45: 1281-96. PMID 412860 DOI: 10.1210/jcem-45-6-1281  1
1977 Devivo DC, Malas D, Nelson JS, Land VJ. Leukoencephalopathy in childhood leukemia. Neurology. 27: 609-13. PMID 267250  1
1977 Chalhub EG, Devivo DC, Siegel BA, Gado MH, Feigin RD. Coxsackie A9 focal encephalitis associated with acute infantile hemiplegia and porencephaly. Neurology. 27: 574-9. PMID 194171  0.68
1977 DeVivo DC, Hahn TJ. Calcium-vitamin D metabolism and the ketogenic diet Annals of Neurology. 2: 255.  1
1976 Chalhub EG, Devivo DC, Volpe JJ. Phenytoin-induced dystonia and choreoathetosis in two retarded epileptic children. Neurology. 26: 494-8. PMID 944401  0.68
1976 Chalhub EG, DeVivo DC. Letter: Phenytoin-induced choreoathetosis. The Journal of Pediatrics. 89: 153-4. PMID 932884 DOI: 10.1016/S0022-3476(76)80956-0  1
1976 Dodson WE, Prensky AL, DeVivo DC, Goldring S, Dodge PR. Management of seizure disorders: selected aspects. Part II. The Journal of Pediatrics. 89: 695-703. PMID 824429 DOI: 10.1016/S0022-3476(76)80786-X  1
1976 Devivo DC, Keating JP. Reye's syndrome. Advances in Pediatrics. 22: 175-229. PMID 817580  1
1976 DeVivo DC, Keating JP, Haymond MW. Acute encephalopathy with fatty infiltration of the viscera. Pediatric Clinics of North America. 23: 527-40. PMID 785351  1
1976 Dodson WE, Prensky AL, DeVivo DC, Goldring S, Dodge PR. Management of seizure disorders: selected aspects. Part I. The Journal of Pediatrics. 89: 527-40. PMID 784928 DOI: 10.1016/S0022-3476(76)80381-2  1
1976 DeVivo DC, Fujimoto K, Leckie MP, Agrawal HC. Subcellular distribution of ketone body metabolizing enzymes in the rat brain. Journal of Neurochemistry. 26: 635-7. PMID 4586  1
1976 Devivo DC. Starvation and Seizures-Reply Archives of Neurology. 33: 377. DOI: 10.1001/archneur.1976.00500050063027  0.68
1975 Greenwood RS, DeVivo DC, Nelson JS, Dodson WE, Raichle ME, Gado M, Haymond MW, Prensky AL. An autosomal dominant form of necrotizing encephalomyelopathy resembling a spinocerebellar degeneration. Transactions of the American Neurological Association. 100: 47-51. PMID 1226640  1
1975 DeVivo DC, Keating JP, Haymond MW. Reye syndrome: results of intensive supportive care. The Journal of Pediatrics. 87: 875-80. PMID 1185388 DOI: 10.1016/S0022-3476(75)80897-3  1
1975 DeVivo DC, Leckie MP, Agrawal HC. D-beta-Hydrozybutyrate: a major precursor of amino acids in developing rat brain. Journal of Neurochemistry. 25: 161-70. PMID 1141913 DOI: 10.1111/j.1471-4159.1975.tb12244.x  1
1975 DeVivo DC, Malas KL, Leckie MP. Starvation and seizures. Observation on the electroconvulsive threshold and cerebral metabolism of the starved adult rat. Archives of Neurology. 32: 755-60. PMID 126678 DOI: 10.1001/archneur.1975.00490530077008  0.68
1974 Appleton DB, DeVivo DC. An animal model for the ketogenic diet. Epilepsia. 15: 211-27. PMID 4525180  1
1974 Hendin B, DeVivo DC, Torack R, Lell ME, Ragab AH, Vietti TJ. Proceedings: Parenchymatous degeneration of the central nervous system in childhood leukemia. Cancer. 33: 468-82. PMID 4521472 DOI: 10.1002/1097-0142(197402)33:2<468::AID-CNCR2820330223>3.0.CO;2-F  1
1974 DeVivo DC, Leckie MP, Agrawal HC. The differential incorporation of D(-) β hydroxybutyrate and glucose into brain amino acids during rat development Trans.Amer.Soc.Neurochem.. 5: 88.  1
1973 Devivo DC, Fishman MA, Agrawal HC. Preferential labeling of brain cholesterol by (3-14C)D(-)-3-hydroxybutyrate. Lipids. 8: 649-51. PMID 4752501 DOI: 10.1007/BF02533150  1
1973 DeVivo DC, Leckie MP, Agrawal HC. The differential incorporation of beta-hydroxybutyrate and glucose into brain glutamate in the newborn rat. Brain Research. 55: 485-90. PMID 4736603 DOI: 10.1016/0006-8993(73)90319-3  1
1973 DeVivo DC, Pagliara AS, Prensky AL. Ketotic hypoglycemia and the ketogenic diet. Neurology. 23: 640-9. PMID 4736310  0.68
1973 Prensky AL, Swisher CN, DeVivo DC. Positive brain scans in children with idiopathic focal epileptic seizures. Neurology. 23: 798-807. PMID 4198225  0.68
1972 Keating JP, DeVivo DC. Reye's syndrome. Missouri Medicine. 69: 861-3. PMID 5080097  1
1972 DeVivo DC, Farrell FW. Vertebrobasilar occlusive disease in children. A recognizable clinical entity. Archives of Neurology. 26: 278-81. PMID 5061289 DOI: 10.1001/archneur.1972.00490090104011  0.68
1971 DeVivo DC, Dodge PR. The critically ill child: diagnosis and management of head injury. Pediatrics. 48: 129-38. PMID 5561864  1
1971 Prensky AL, DeVivo DC, Palkes H. Severe bradykinesia as a manifestation of toxicity to antiepileptic medications. The Journal of Pediatrics. 78: 700-4. PMID 5547831 DOI: 10.1016/S0022-3476(71)80481-X  1
1971 DeVivo DC. Cerebral abscess in children. Developmental Medicine and Child Neurology. 13: 800-4. PMID 4944988  1
1971 Feigin RD, Shackelford PG, Haymond MW, DeVivo DC. Floxuridine treatment of congenital cytomegalic inclusion disease. Pediatrics. 48: 318-22. PMID 4327111  1
1970 Quarfordt SH, DeVivo DC, Engel WK, Levy RI, Fredrickson DS. Familial adult-onset proximal spinal muscular atrophy. Report of a family with type II hyperlipoproteinemia. Archives of Neurology. 22: 541-9. PMID 5439897 DOI: 10.1001/archneur.1970.00480240061009  0.68
1970 DeVivo DC, Peterkofsky B. The effect of alpha-ketoglutarate and other alpha-keto acids on the recovery of tyrosine aminotransferase activity from chick embryo liver. The Journal of Biological Chemistry. 245: 2737-46. PMID 4393297  0.68
1970 DeVivo DC, Engel WK. Remarkable recovery of a steroid-responsive recurrent polyneuropathy. Journal of Neurology, Neurosurgery, and Psychiatry. 33: 62-9. PMID 4313855  1
1965 DeVivo D, Kline E, Dodge PR. Influence of human cerebrospinal fluid on blood coagulation in vitro. Archives of Neurology. 13: 615-20. PMID 5850668 DOI: 10.1001/archneur.1965.00470060051004  0.68
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