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I Tein

Showing results (31-40 of 39) with videos related to

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Mitochondrion|March 25, 2015
Cerebral hyperperfusion and decreased cerebrovascular reactivity correlate with neurologic disease severity in MELASL H Rodan, J Poublanc, J A Fisher, et al.
Human Mutation|March 25, 1999
Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunctionS Raha, F Merante, E Shoubridge, et al.
Annals of Neurology|September 1, 1991
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathyI Tein, D C De Vivo, D E Hale, et al.
The Journal of Clinical Investigation|September 17, 1998
Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlationJ A Ibdah, I Tein, C Dionisi-Vici, et al.
Pediatric Research|November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiencyR Pons, R Carrozzo, I Tein, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 21, 2004
Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathyM Kinali, S E Olpin, P T Clayton, et al.
Annals of Neurology|July 1, 1993
Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observationsB Koo, L E Becker, S Chuang, et al.
Epilepsia|November 20, 1998
L-carnitine supplementation in childhood epilepsy: current perspectivesD C De Vivo, T P Bohan, D L Coulter, et al.
Pediatric Research|September 1, 1990
Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathyI Tein, D C De Vivo, F Bierman, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
Mitochondrion|March 25, 2015
Cerebral hyperperfusion and decreased cerebrovascular reactivity correlate with neurologic disease severity in MELASL H Rodan, J Poublanc, J A Fisher, et al.
Human Mutation|March 25, 1999
Repopulation of rho0 cells with mitochondria from a patient with a mitochondrial DNA point mutation in tRNA(Gly) results in respiratory chain dysfunctionS Raha, F Merante, E Shoubridge, et al.
Annals of Neurology|September 1, 1991
Short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency in muscle: a new cause for recurrent myoglobinuria and encephalopathyI Tein, D C De Vivo, D E Hale, et al.
The Journal of Clinical Investigation|September 17, 1998
Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlationJ A Ibdah, I Tein, C Dionisi-Vici, et al.
Pediatric Research|November 14, 1997
Deficient muscle carnitine transport in primary carnitine deficiencyR Pons, R Carrozzo, I Tein, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 21, 2004
Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathyM Kinali, S E Olpin, P T Clayton, et al.
Annals of Neurology|July 1, 1993
Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observationsB Koo, L E Becker, S Chuang, et al.
Epilepsia|November 20, 1998
L-carnitine supplementation in childhood epilepsy: current perspectivesD C De Vivo, T P Bohan, D L Coulter, et al.
Pediatric Research|September 1, 1990
Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathyI Tein, D C De Vivo, F Bierman, et al.
Pageof 4