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M J Bennett

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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.
Journal of Inherited Metabolic Disease|January 1, 1993
Juvenile neuronal ceroid-lipofuscinosis: characterization of the dyslipoproteinaemia and demonstration of membrane phospholipid and phospholipid-dependent signal transduction abnormalities in cultured skin fibroblastsM J Bennett, S F Poirier, L Chern, 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.
The Australian Journal of Advanced Nursing : a Quarterly Publication of the Royal Australian Nursing Federation|June 1, 1985
Leg ulcer management at homeM J Bennett, J F Cummane, I Halstead-Smith, et al.
Lancet (London, England)|February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant deathM J Bennett, F Allison, R J Pollitt, 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.
Pageof 36

Showing results (301-310 of 351) with videos related to

Sort By:
Pageof 36
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.
Journal of Inherited Metabolic Disease|January 1, 1993
Juvenile neuronal ceroid-lipofuscinosis: characterization of the dyslipoproteinaemia and demonstration of membrane phospholipid and phospholipid-dependent signal transduction abnormalities in cultured skin fibroblastsM J Bennett, S F Poirier, L Chern, 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.
The Australian Journal of Advanced Nursing : a Quarterly Publication of the Royal Australian Nursing Federation|June 1, 1985
Leg ulcer management at homeM J Bennett, J F Cummane, I Halstead-Smith, et al.
Lancet (London, England)|February 21, 1987
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant deathM J Bennett, F Allison, R J Pollitt, 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.
Pageof 36