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Biotechniques|August 19, 2000

Transfer and expression of foreign genes in mammalian cellsA Colosimo, K K Goncz, A R Holmes, et al.

Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 29, 1999

Fatal hepatic short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: clinical, biochemical, and pathological studies on three subjects with this recently identified disorder of mitochondrial beta-oxidationM J Bennett, S D Spotswood, K F Ross, et al.

Pediatric Research|September 1, 1996

Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant alleleJ D Isaacs, H F Sims, C K Powell, et al.

Journal of Inherited Metabolic Disease|January 1, 1993

Reliable prenatal diagnosis of Canavan disease (aspartoacylase deficiency): comparison of enzymatic and metabolite analysisM J Bennett, K M Gibson, W G Sherwood, et al.

The Journal of Pediatrics|December 1, 1992

3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defectsK M Gibson, M J Bennett, C E Mize, et al.

The Journal of Clinical Investigation|September 17, 1998

Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlationJ A Ibdah, I Tein, C Dionisi-Vici, et al.

The Journal of Pediatrics|August 10, 2000

Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family studyE P Treacy, D M Lambert, R Barnes, et al.

Journal of Inherited Metabolic Disease|January 1, 1990

Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, P M Coates, D E Hale, et al.

Journal of Inherited Metabolic Disease|January 1, 1984

Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatallyM J Bennett, D A Curnock, P C Engel, et al.

Clinical Chemistry|June 28, 2001

Accumulation of free 3-hydroxy fatty acids in the culture media of fibroblasts from patients deficient in long-chain l-3-hydroxyacyl-CoA dehydrogenase: a useful diagnostic aidP M Jones, M Moffitt, D Joseph, et al.

Pageof 25

Showing results (201-210 of 245) with videos related to

Sort By:

Pageof 25

Biotechniques|August 19, 2000

Transfer and expression of foreign genes in mammalian cellsA Colosimo, K K Goncz, A R Holmes, et al.

Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|May 29, 1999

Fatal hepatic short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: clinical, biochemical, and pathological studies on three subjects with this recently identified disorder of mitochondrial beta-oxidationM J Bennett, S D Spotswood, K F Ross, et al.

Pediatric Research|September 1, 1996

Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant alleleJ D Isaacs, H F Sims, C K Powell, et al.

Journal of Inherited Metabolic Disease|January 1, 1993

Reliable prenatal diagnosis of Canavan disease (aspartoacylase deficiency): comparison of enzymatic and metabolite analysisM J Bennett, K M Gibson, W G Sherwood, et al.

The Journal of Pediatrics|December 1, 1992

3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defectsK M Gibson, M J Bennett, C E Mize, et al.

The Journal of Clinical Investigation|September 17, 1998

Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlationJ A Ibdah, I Tein, C Dionisi-Vici, et al.

The Journal of Pediatrics|August 10, 2000

Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family studyE P Treacy, D M Lambert, R Barnes, et al.

Journal of Inherited Metabolic Disease|January 1, 1990

Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, P M Coates, D E Hale, et al.

Journal of Inherited Metabolic Disease|January 1, 1984

Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatallyM J Bennett, D A Curnock, P C Engel, et al.

Clinical Chemistry|June 28, 2001

Accumulation of free 3-hydroxy fatty acids in the culture media of fibroblasts from patients deficient in long-chain l-3-hydroxyacyl-CoA dehydrogenase: a useful diagnostic aidP M Jones, M Moffitt, D Joseph, et al.

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