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Showing results (11-20 of 18) with videos related to

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Journal of Inherited Metabolic Disease|October 25, 2008
Tetrahydrobiopterin deficiency in human rabiesR E Willoughby, T Opladen, T Maier, et al.
Human Genetics|August 1, 1991
The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the geneS Kølvraa, N Gregersen, A I Blakemore, et al.
Journal of Clinical Pharmacology|June 19, 2013
Population pharmacokinetic modeling and dosing simulations of nitrogen-scavenging compounds: disposition of glycerol phenylbutyrate and sodium phenylbutyrate in adult and pediatric patients with urea cycle disordersJon P R Monteleone, M Mokhtarani, G A Diaz, et al.
Molecular Genetics and Metabolism|May 27, 2011
Ammonia control in children with urea cycle disorders (UCDs); phase 2 comparison of sodium phenylbutyrate and glycerol phenylbutyrateUta Lichter-Konecki, G A Diaz, J L Merritt, et al.
Journal of Inherited Metabolic Disease|November 1, 2002
Phenylketonuria in adulthood: a collaborative studyR Koch, B Burton, G Hoganson, et al.
Molecular Genetics and Metabolism|November 21, 2015
Glutamine and hyperammonemic crises in patients with urea cycle disordersB Lee, G A Diaz, W Rhead, et al.
Molecular Genetics and Metabolism|October 23, 2013
Elevated phenylacetic acid levels do not correlate with adverse events in patients with urea cycle disorders or hepatic encephalopathy and can be predicted based on the plasma PAA to PAGN ratioM Mokhtarani, G A Diaz, W Rhead, et al.
Molecular Genetics and Metabolism|September 11, 2012
Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disordersM Mokhtarani, G A Diaz, W Rhead, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Journal of Inherited Metabolic Disease|October 25, 2008
Tetrahydrobiopterin deficiency in human rabiesR E Willoughby, T Opladen, T Maier, et al.
Human Genetics|August 1, 1991
The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the geneS Kølvraa, N Gregersen, A I Blakemore, et al.
Journal of Clinical Pharmacology|June 19, 2013
Population pharmacokinetic modeling and dosing simulations of nitrogen-scavenging compounds: disposition of glycerol phenylbutyrate and sodium phenylbutyrate in adult and pediatric patients with urea cycle disordersJon P R Monteleone, M Mokhtarani, G A Diaz, et al.
Molecular Genetics and Metabolism|May 27, 2011
Ammonia control in children with urea cycle disorders (UCDs); phase 2 comparison of sodium phenylbutyrate and glycerol phenylbutyrateUta Lichter-Konecki, G A Diaz, J L Merritt, et al.
Journal of Inherited Metabolic Disease|November 1, 2002
Phenylketonuria in adulthood: a collaborative studyR Koch, B Burton, G Hoganson, et al.
Molecular Genetics and Metabolism|November 21, 2015
Glutamine and hyperammonemic crises in patients with urea cycle disordersB Lee, G A Diaz, W Rhead, et al.
Molecular Genetics and Metabolism|October 23, 2013
Elevated phenylacetic acid levels do not correlate with adverse events in patients with urea cycle disorders or hepatic encephalopathy and can be predicted based on the plasma PAA to PAGN ratioM Mokhtarani, G A Diaz, W Rhead, et al.
Molecular Genetics and Metabolism|September 11, 2012
Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disordersM Mokhtarani, G A Diaz, W Rhead, et al.
Pageof 2