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I Tein

Showing results (11-20 of 39) with videos related to

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The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1996
Addison's disease presenting with cerebral edemaC Geenen, I Tein, R M Ehrlich
Advances in Pediatrics|January 1, 1990
Recurrent childhood myoglobinuriaI Tein, S DiMauro, D C DeVivo
Archives of Biochemistry and Biophysics|May 15, 1996
Characterization of the human plasmalemmal carnitine transporter in cultured skin fibroblastsI Tein, S W Bukovac, Z W Xie
Neurology|February 20, 1999
Long-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency neuropathy: response to cod liver oilI Tein, J Vajsar, L MacMillan, et al.
American Journal of Human Genetics|September 1, 1994
Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) geneF Merante, I Tein, L Benson, et al.
The Journal of Pediatrics|June 1, 1994
Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitisI Tein, J Christodoulou, E Donner, et al.
Pediatric Cardiology|December 31, 2000
Maternally inherited hypertrophic cardiomyopathy: a manifestation of mitochondrial DNA mutations--clinical course in two familiesA I Dipchand, I Tein, B Robinson, et al.
Journal of the Neurological Sciences|September 1, 1989
Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts. Tissue specific isoforms of CPT1?I Tein, F Demaugre, J P Bonnefont, et al.
Journal of Inherited Metabolic Disease|March 18, 2003
Glucose-free medium exacerbates microvesicular steatosis in cultured skin fibroblasts of genetic defects of fatty acid oxidation. A novel screening testD L Renaud, V Edwards, G J Wilson, et al.
Progress in Clinical and Biological Research|January 1, 1990
Hepatic and muscular forms of palmitoyl carnitine transferase deficiencyJ P Bonnefont, I Tein, J M Saudubray, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1996
Addison's disease presenting with cerebral edemaC Geenen, I Tein, R M Ehrlich
Advances in Pediatrics|January 1, 1990
Recurrent childhood myoglobinuriaI Tein, S DiMauro, D C DeVivo
Archives of Biochemistry and Biophysics|May 15, 1996
Characterization of the human plasmalemmal carnitine transporter in cultured skin fibroblastsI Tein, S W Bukovac, Z W Xie
Neurology|February 20, 1999
Long-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency neuropathy: response to cod liver oilI Tein, J Vajsar, L MacMillan, et al.
American Journal of Human Genetics|September 1, 1994
Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) geneF Merante, I Tein, L Benson, et al.
The Journal of Pediatrics|June 1, 1994
Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitisI Tein, J Christodoulou, E Donner, et al.
Pediatric Cardiology|December 31, 2000
Maternally inherited hypertrophic cardiomyopathy: a manifestation of mitochondrial DNA mutations--clinical course in two familiesA I Dipchand, I Tein, B Robinson, et al.
Journal of the Neurological Sciences|September 1, 1989
Normal muscle CPT1 and CPT2 activities in hepatic presentation patients with CPT1 deficiency in fibroblasts. Tissue specific isoforms of CPT1?I Tein, F Demaugre, J P Bonnefont, et al.
Journal of Inherited Metabolic Disease|March 18, 2003
Glucose-free medium exacerbates microvesicular steatosis in cultured skin fibroblasts of genetic defects of fatty acid oxidation. A novel screening testD L Renaud, V Edwards, G J Wilson, et al.
Progress in Clinical and Biological Research|January 1, 1990
Hepatic and muscular forms of palmitoyl carnitine transferase deficiencyJ P Bonnefont, I Tein, J M Saudubray, et al.
Pageof 4