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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 storage
T 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 disease
T 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 specimens
T Hagen, M S Korson, M Sakamoto, et al.
The Journal of Pediatrics
|
May 1, 1996
Oxidative phosphorylation defect associated with primary adrenal insufficiency
K 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 acids
L 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 enzyme
T 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 kidneys
K 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 disease
B 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 deficiency
G 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 management
K N North, M S Korson, Y R Gopal, et al.
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of 2
Search research articles
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Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 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 storage
T 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 disease
T 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 specimens
T Hagen, M S Korson, M Sakamoto, et al.
The Journal of Pediatrics
|
May 1, 1996
Oxidative phosphorylation defect associated with primary adrenal insufficiency
K 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 acids
L 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 enzyme
T 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 kidneys
K 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 disease
B 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 deficiency
G 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 management
K N North, M S Korson, Y R Gopal, et al.
Page
of 2