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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.European Journal of Pediatrics|May 20, 1999
N-acetylaspartylglutamate in Canavan disease: an adverse effector?A P Burlina, V Ferrari, P Divry, et al.Prenatal Diagnosis|February 1, 1987
Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiencyM J Bennett, F Allison, G W Lowther, et al.The Journal of Clinical Investigation|June 8, 2001
Lack of mitochondrial trifunctional protein in mice causes neonatal hypoglycemia and sudden deathJ A Ibdah, H Paul, Y Zhao, et al.Steroids|September 1, 1996
Mammalian 3 alpha-hydroxysteroid dehydrogenasesT M Penning, J E Pawlowski, B P Schlegel, et al.Perioperative Medicine (London, England)|April 24, 2025
The impact of frailty on functional recovery after cardiac surgery-a case control studyM Abdelmonem, M Elsayed, D Awadallah, et al.Pageof 25