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M S Korson

Showing results (1-10 of 13) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|May 26, 1999
Quantification of glutaric acid by isotope dilution mass spectrometry for patients with glutaric acidemia type I: selected ion monitoring vs. selected ion storageT Hagen, M S Korson
Molecular Genetics and Metabolism|August 5, 2000
Urinary lactate excretion to monitor the efficacy of treatment of type I glycogen storage diseaseT Hagen, M S Korson, J I Wolfsdorf
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1999
A GC/MS/MS screening method for multiple organic acidemias from urine specimensT Hagen, M S Korson, M Sakamoto, et al.
The Journal of Pediatrics|May 1, 1996
Oxidative phosphorylation defect associated with primary adrenal insufficiencyK North, M S Korson, N Krawiecki, et al.
The Journal of Pediatrics|September 20, 2001
Tyrosine supplementation in phenylketonuria: diurnal blood tyrosine levels and presumptive brain influx of tyrosine and other large neutral amino acidsL R Kalsner, F J Rohr, K A Strauss, et al.
Journal of Pediatric Ophthalmology and Strabismus|November 1, 1995
Bilateral infantile cataractogenesis in a patient with deficiency of complex I, a mitochondrial electron transport chain enzymeT A Ciulla, K North, O McCabe, et al.
The Journal of Pediatrics|September 1, 1995
Lethal neonatal deficiency of carnitine palmitoyltransferase II associated with dysgenesis of the brain and kidneysK N North, C L Hoppel, U De Girolami, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|September 3, 1999
Quality of life assessment in adults with type 1 Gaucher diseaseB J Masek, K B Sims, C M Bove, et al.
The Journal of Pediatrics|August 26, 1998
Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiencyG F Cox, M Souri, T Aoyama, et al.
The Journal of Pediatrics|June 1, 1995
Neonatal-onset propionic acidemia: neurologic and developmental profiles, and implications for managementK N North, M S Korson, Y R Gopal, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 26, 1999
Quantification of glutaric acid by isotope dilution mass spectrometry for patients with glutaric acidemia type I: selected ion monitoring vs. selected ion storageT Hagen, M S Korson
Molecular Genetics and Metabolism|August 5, 2000
Urinary lactate excretion to monitor the efficacy of treatment of type I glycogen storage diseaseT Hagen, M S Korson, J I Wolfsdorf
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 15, 1999
A GC/MS/MS screening method for multiple organic acidemias from urine specimensT Hagen, M S Korson, M Sakamoto, et al.
The Journal of Pediatrics|May 1, 1996
Oxidative phosphorylation defect associated with primary adrenal insufficiencyK North, M S Korson, N Krawiecki, et al.
The Journal of Pediatrics|September 20, 2001
Tyrosine supplementation in phenylketonuria: diurnal blood tyrosine levels and presumptive brain influx of tyrosine and other large neutral amino acidsL R Kalsner, F J Rohr, K A Strauss, et al.
Journal of Pediatric Ophthalmology and Strabismus|November 1, 1995
Bilateral infantile cataractogenesis in a patient with deficiency of complex I, a mitochondrial electron transport chain enzymeT A Ciulla, K North, O McCabe, et al.
The Journal of Pediatrics|September 1, 1995
Lethal neonatal deficiency of carnitine palmitoyltransferase II associated with dysgenesis of the brain and kidneysK N North, C L Hoppel, U De Girolami, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|September 3, 1999
Quality of life assessment in adults with type 1 Gaucher diseaseB J Masek, K B Sims, C M Bove, et al.
The Journal of Pediatrics|August 26, 1998
Reversal of severe hypertrophic cardiomyopathy and excellent neuropsychologic outcome in very-long-chain acyl-coenzyme A dehydrogenase deficiencyG F Cox, M Souri, T Aoyama, et al.
The Journal of Pediatrics|June 1, 1995
Neonatal-onset propionic acidemia: neurologic and developmental profiles, and implications for managementK N North, M S Korson, Y R Gopal, et al.
Pageof 2