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Medium-chain acyl-CoA dehydrogenase deficiency: postmortem diagnosis in a case of sudden infant death and neonatal diagnosis of an affected sibling.
Bennett MJ, Rinaldo P, Millington DS, Tanaka K, Yokota I, Coates PM. Bennett MJ, et al. Pediatr Pathol. 1991 Nov-Dec;11(6):889-95. doi: 10.3109/15513819109065485. Pediatr Pathol. 1991. PMID: 1775402
Postmortem recognition of fatty acid oxidation disorders.
Bennett MJ, Hale DE, Coates PM, Stanley CA. Bennett MJ, et al. Pediatr Pathol. 1991 May-Jun;11(3):365-70. doi: 10.3109/15513819109064772. Pediatr Pathol. 1991. PMID: 1866359
Renal handling of carnitine in secondary carnitine deficiency disorders.
Stanley CA, Berry GT, Bennett MJ, Willi SM, Treem WR, Hale DE. Stanley CA, et al. Pediatr Res. 1993 Jul;34(1):89-97. doi: 10.1203/00006450-199307000-00021. Pediatr Res. 1993. PMID: 8356025
The laboratory diagnosis of inborn errors of mitochondrial fatty acid oxidation.
Bennett MJ. Bennett MJ. Ann Clin Biochem. 1990 Nov;27 ( Pt 6):519-31. doi: 10.1177/000456329002700602. Ann Clin Biochem. 1990. PMID: 2080855 Review. No abstract available.
Comparison of post-mortem urinary and vitreous humour organic acids.
Bennett MJ, Ragni MC, Hood I, Hale DE. Bennett MJ, et al. Ann Clin Biochem. 1992 Sep;29 ( Pt 5):541-5. doi: 10.1177/000456329202900509. Ann Clin Biochem. 1992. PMID: 1444166
Mitochondrial respiratory chain disease discrimination by retrospective cohort analysis of blood metabolites.
Clarke C, Xiao R, Place E, Zhang Z, Sondheimer N, Bennett M, Yudkoff M, Falk MJ. Clarke C, et al. Mol Genet Metab. 2013 Sep-Oct;110(1-2):145-52. doi: 10.1016/j.ymgme.2013.07.011. Epub 2013 Jul 19. Mol Genet Metab. 2013. PMID: 23920046 Free PMC article.
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