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J M Land

Showing results (81-90 of 83) with videos related to

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Journal of Inherited Metabolic Disease|May 11, 1999
The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial diseaseJ R Bonham, P Guthrie, M Downing, et al.
Mitochondrion|July 11, 2014
Successful reversal of propionic acidaemia associated cardiomyopathy: evidence for low myocardial coenzyme Q10 status and secondary mitochondrial dysfunction as an underlying pathophysiological mechanismJ Baruteau, I Hargreaves, S Krywawych, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.
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Showing results (81-90 of 83) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 83 results.
Journal of Inherited Metabolic Disease|May 11, 1999
The allopurinol load test lacks specificity for primary urea cycle defects but may indicate unrecognized mitochondrial diseaseJ R Bonham, P Guthrie, M Downing, et al.
Mitochondrion|July 11, 2014
Successful reversal of propionic acidaemia associated cardiomyopathy: evidence for low myocardial coenzyme Q10 status and secondary mitochondrial dysfunction as an underlying pathophysiological mechanismJ Baruteau, I Hargreaves, S Krywawych, et al.
Journal of Inherited Metabolic Disease|November 8, 2003
Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiencyS E Olpin, A Afifi, S Clark, et al.
Pageof 9