Bennett MJ - Search Results

1

Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

Enns GM, Bennett MJ, Hoppel CL, Goodman SI, Weisiger K, Ohnstad C, Golabi M, Packman S. Enns GM, et al. Among authors: bennett mj. J Pediatr. 2000 Feb;136(2):251-4. doi: 10.1016/s0022-3476(00)70111-9. J Pediatr. 2000. PMID: 10657835

2

Early neonatal diagnosis of long-chain 3-hydroxyacyl coenzyme a dehydrogenase and mitochondrial trifunctional protein deficiencies.

Hintz SR, Matern D, Strauss A, Bennett MJ, Hoyme HE, Schelley S, Kobori J, Colby C, Lehman NL, Enns GM. Hintz SR, et al. Among authors: bennett mj. Mol Genet Metab. 2002 Feb;75(2):120-7. doi: 10.1006/mgme.2001.3282. Mol Genet Metab. 2002. PMID: 11855930

3

Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency.

Bhala A, Willi SM, Rinaldo P, Bennett MJ, Schmidt-Sommerfeld E, Hale DE. Bhala A, et al. Among authors: bennett mj. J Pediatr. 1995 Jun;126(6):910-5. doi: 10.1016/s0022-3476(95)70207-5. J Pediatr. 1995. PMID: 7776094

4

Short-chain hydroxyacyl-coenzyme A dehydrogenase deficiency presenting as unexpected infant death: A family study.

Treacy EP, Lambert DM, Barnes R, Boriack RL, Vockley J, O'brien LK, Jones PM, Bennett MJ. Treacy EP, et al. Among authors: bennett mj. J Pediatr. 2000 Aug;137(2):257-9. doi: 10.1067/mpd.2000.107467. J Pediatr. 2000. PMID: 10931422

5

Limitations of 3-phenylpropionylglycine in early screening for medium-chain acyl-coenzyme A dehydrogenase deficiency.

Bhala A, Bennett MJ, McGowan KL, Hale DE. Bhala A, et al. Among authors: bennett mj. J Pediatr. 1993 Jan;122(1):100-3. doi: 10.1016/s0022-3476(05)83499-7. J Pediatr. 1993. PMID: 8419594

6

Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid beta-oxidation.

Jones PM, Quinn R, Fennessey PV, Tjoa S, Goodman SI, Fiore S, Burlina AB, Rinaldo P, Boriack RL, Bennett MJ. Jones PM, et al. Among authors: bennett mj. Clin Chem. 2000 Feb;46(2):149-55. Clin Chem. 2000. PMID: 10657369

7

Very long-chain acyl-CoA dehydrogenase deficiency in a patient with normal newborn screening by tandem mass spectrometry.

Ficicioglu C, Coughlin CR 2nd, Bennett MJ, Yudkoff M. Ficicioglu C, et al. Among authors: bennett mj. J Pediatr. 2010 Mar;156(3):492-4. doi: 10.1016/j.jpeds.2009.10.031. Epub 2010 Jan 8. J Pediatr. 2010. PMID: 20056241

8

Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder.

Bennett MJ, Pollitt RJ, Goodman SI, Hale DE, Vamecq J. Bennett MJ, et al. J Inherit Metab Dis. 1991;14(2):165-73. doi: 10.1007/BF01800589. J Inherit Metab Dis. 1991. PMID: 1909402

9

Stability of long-chain and short-chain 3-hydroxyacyl-CoA dehydrogenase activity in postmortem liver.

Hale DE, Cornell JE, Bennett MJ. Hale DE, et al. Among authors: bennett mj. Clin Chem. 1997 Feb;43(2):273-8. Clin Chem. 1997. PMID: 9023129

10

Heterozygosity for long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency and deterioration in liver function in a newborn infant infected with human immunodeficiency virus.

Hicks P, Bennett MJ, Squires J, Ramilo O. Hicks P, et al. Among authors: bennett mj. J Pediatr. 1995 Oct;127(4):599-602. doi: 10.1016/s0022-3476(95)70122-2. J Pediatr. 1995. PMID: 7562284

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