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William J Rhead

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

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Molecular Genetics and Metabolism|March 27, 2002
Evaluation of liver fatty acid oxidation in the leptin-deficient obese mouseAmy E Brix, Ada Elgavish, Tim R Nagy, et al.
The New England Journal of Medicine|June 1, 2007
Survival after treatment with phenylacetate and benzoate for urea-cycle disordersGregory M Enns, Susan A Berry, Gerard T Berry, et al.
Critical Care Clinics|October 18, 2005
Urea cycle disorders: clinical presentation outside the newborn periodWendy Smith, Priya S Kishnani, Brendan Lee, et al.
Critical Care Clinics|October 18, 2005
Unmasked adult-onset urea cycle disorders in the critical care settingMarshall L Summar, Frederick Barr, Sheila Dawling, et al.
Clinical Chemistry|July 4, 2009
National academy of clinical biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summaryDennis J Dietzen, Piero Rinaldo, Ronald J Whitley, et al.
Journal of Magnetic Resonance Imaging : JMRI|September 25, 2004
Ascorbate decreases Fabry cerebral hyperperfusion suggesting a reactive oxygen species abnormality: an arterial spin tagging studyDavid F Moore, Frank Ye, Marie-Luise Brennan, et al.
Human Mutation|November 20, 2010
Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172BGladys Ho, Atsushi Yonezawa, Satohiro Masuda, et al.
American Journal of Human Genetics|January 24, 2012
Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndromePhilippe M Campeau, Jaeseung C Kim, James T Lu, 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.
Molecular Genetics and Metabolism|March 27, 2002
Evaluation of liver fatty acid oxidation in the leptin-deficient obese mouseAmy E Brix, Ada Elgavish, Tim R Nagy, et al.
The New England Journal of Medicine|June 1, 2007
Survival after treatment with phenylacetate and benzoate for urea-cycle disordersGregory M Enns, Susan A Berry, Gerard T Berry, et al.
Critical Care Clinics|October 18, 2005
Urea cycle disorders: clinical presentation outside the newborn periodWendy Smith, Priya S Kishnani, Brendan Lee, et al.
Critical Care Clinics|October 18, 2005
Unmasked adult-onset urea cycle disorders in the critical care settingMarshall L Summar, Frederick Barr, Sheila Dawling, et al.
Clinical Chemistry|July 4, 2009
National academy of clinical biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summaryDennis J Dietzen, Piero Rinaldo, Ronald J Whitley, et al.
Journal of Magnetic Resonance Imaging : JMRI|September 25, 2004
Ascorbate decreases Fabry cerebral hyperperfusion suggesting a reactive oxygen species abnormality: an arterial spin tagging studyDavid F Moore, Frank Ye, Marie-Luise Brennan, et al.
Human Mutation|November 20, 2010
Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172BGladys Ho, Atsushi Yonezawa, Satohiro Masuda, et al.
American Journal of Human Genetics|January 24, 2012
Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndromePhilippe M Campeau, Jaeseung C Kim, James T Lu, et al.
Pageof 2