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Results of search for 'au:"Devivo, D C"', page 3 of 4
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Agrawal, H C
Bonilla, E
Brooke, M H
Carroll, J E
Chalhub, E G
DeVivo, D C
Devivo, D C
DiMauro, S
Dodge, P R
Dodson, W E
Feigin, R D
Haymond, M W
Hays, A P
Hirano, M
Keating, J P
Leckie, M P
Nelson, J S
Pavlakis, S G
Prensky, A L
Schon, E A
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Your search returned 75 results.
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41.
Mitochondrial morphology and intracellular calcium homeostasis in cytochrome oxidase-deficient human fibroblasts.
[electronic resource]
by
Handran, S D
Werth, J L
DeVivo, D C
Rothman, S M
Producer:
19970717
In:
Neurobiology of disease
vol. 3
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42.
Hepatic metabolites and uric acid excretion in fructose-1,6-diphosphatase deficiency.
[electronic resource]
by
Velázquez, A
DeCéspedes, C
DeVivo, D C
Costin, G
Shaw, K N
Producer:
19890412
In:
Journal of inherited metabolic disease
vol. 11
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43.
The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome.
[electronic resource]
by
Santorelli, F M
Shanske, S
Macaya, A
DeVivo, D C
DiMauro, S
Producer:
19940104
In:
Annals of neurology
vol. 34
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44.
Letter: Hypophosphataemia in Reye's syndrome.
[electronic resource]
by
Keating, J P
Karl, I E
DeVivo, D C
Haymond, M W
Producer:
19751010
In:
Lancet (London, England)
vol. 2
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45.
Metabolic response to hypertonic glucose administration in Reye syndrome.
[electronic resource]
by
Haymond, M W
Karl, I E
Keating, J P
DeVivo, D C
Producer:
19780814
In:
Annals of neurology
vol. 3
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46.
Congenital astrocytoma presenting with intracerebral hematoma. Case report.
[electronic resource]
by
Rothman, S M
Nelson, J S
DeVivo, D C
Coxe, W S
Producer:
19790901
In:
Journal of neurosurgery
vol. 51
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47.
Management of seizure disorders: selected aspects. Part II.
[electronic resource]
by
Dodson, W E
Prensky, A L
DeVivo, D C
Goldring, S
Dodge, P R
Producer:
19761223
In:
The Journal of pediatrics
vol. 89
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48.
Management of seizure disorders: selected aspects. Part I.
[electronic resource]
by
Dodson, W E
Prensky, A L
DeVivo, D C
Goldring, S
Dodge, P R
Producer:
19761101
In:
The Journal of pediatrics
vol. 89
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49.
Mitochondrial myopathies.
[electronic resource]
by
DiMauro, S
Bonilla, E
Zeviani, M
Servidei, S
DeVivo, D C
Schon, E A
Producer:
19880113
In:
Journal of inherited metabolic disease
vol. 10 Suppl 1
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50.
SSPE, measles virus, and the matrix protein: report of a case with unusual immunochemical findings.
[electronic resource]
by
Mandelbaum, D E
Hall, W W
Paneth, N
Wolff, R R
DeVivo, D C
Producer:
19820222
In:
Annals of neurology
vol. 10
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51.
Fasting as a provocative test in neuromuscular diseases.
[electronic resource]
by
Carroll, J E
DeVivo, D C
Brooke, M H
Planer, G J
Hagberg, J H
Producer:
19790816
In:
Metabolism: clinical and experimental
vol. 28
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52.
Familial adult-onset proximal spinal muscular atrophy. Report of a family with type II hyperlipoproteinemia.
[electronic resource]
by
Quarfordt, S H
DeVivo, D C
Engel, W K
Levy, R I
Fredrickson, D S
Producer:
19700604
In:
Archives of neurology
vol. 22
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53.
Reye syndrome complicated by a generalized herpes simplex type I infection.
[electronic resource]
by
Chalhub, E G
DeVivo, D C
Keating, J P
Haymond, M W
Feigin, R D
Producer:
19810317
In:
The Journal of pediatrics
vol. 98
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54.
Coxsackie A9 focal encephalitis associated with acute infantile hemiplegia and porencephaly.
[electronic resource]
by
Chalhub, E G
Devivo, D C
Siegel, B A
Gado, M H
Feigin, R D
Producer:
19770718
In:
Neurology
vol. 27
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55.
Biochemical and physiologic consequences of carnitine palmityltransferase deficiency.
[electronic resource]
by
Carroll, J E
Brooke, M H
DeVivo, D C
Kaiser, K K
Hagberg, J M
Producer:
19790716
In:
Muscle & nerve
vol. 1
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56.
Defective activation of the pyruvate dehydrogenase complex in subacute necrotizing encephalomyelopathy (Leigh disease).
[electronic resource]
by
DeVivo, D C
Haymond, M W
Obert, K A
Nelson, J S
Pagliara, A S
Producer:
19800426
In:
Annals of neurology
vol. 6
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57.
Middle cerebral artery blood velocity and cerebral blood flow in sickle cell disease.
[electronic resource]
by
Brass, L M
Prohovnik, I
Pavlakis, S G
DeVivo, D C
Piomelli, S
Mohr, J P
Producer:
19910219
In:
Stroke
vol. 22
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58.
Proceedings: Parenchymatous degeneration of the central nervous system in childhood leukemia.
[electronic resource]
by
Hendin, B
DeVivo, D C
Torack, R
Lell, M E
Ragab, A H
Vietti, T J
Producer:
19740404
In:
Cancer
vol. 33
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59.
Benign infantile mitochondrial myopathy due to reversible cytochrome c oxidase deficiency.
[electronic resource]
by
DiMauro, S
Nicholson, J F
Hays, A P
Eastwood, A B
Koenigsberger, R
DeVivo, D C
Producer:
19830225
In:
Transactions of the American Neurological Association
vol. 106
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60.
Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutations.
[electronic resource]
by
Vázquez-Memije, M E
Shanske, S
Santorelli, F M
Kranz-Eble, P
DeVivo, D C
DiMauro, S
Producer:
19990305
In:
Journal of inherited metabolic disease
vol. 21
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