Millington DS - Search Results

1

Significance of bound glutarate in the diagnosis of glutaric aciduria type I.

Ribes A, Riudor E, Briones P, Christensen E, Campistol J, Millington DS. Ribes A, et al. Among authors: millington ds. J Inherit Metab Dis. 1992;15(3):367-70. doi: 10.1007/BF02435978. J Inherit Metab Dis. 1992. PMID: 1405471 No abstract available.

2

Glutaric aciduria type I: unusual biochemical presentation.

Campistol J, Ribes A, Alvarez L, Christensen E, Millington DS. Campistol J, et al. Among authors: millington ds. J Pediatr. 1992 Jul;121(1):83-6. doi: 10.1016/s0022-3476(05)82548-x. J Pediatr. 1992. PMID: 1625098

3

L-Carnitine insufficiency in disorders of organic acid metabolism: response to L-carnitine by patients with methylmalonic aciduria and 3-hydroxy-3-methylglutaric aciduria.

Chalmers RA, Stacey TE, Tracey BM, de Sousa C, Roe CR, Millington DS, Hoppel CL. Chalmers RA, et al. Among authors: millington ds. J Inherit Metab Dis. 1984;7 Suppl 2:109-10. doi: 10.1007/978-94-009-5612-4_29. J Inherit Metab Dis. 1984. PMID: 6207380 No abstract available.

4

Acylcarnitines in amniotic fluid: application to the prenatal diagnosis of propionic acidaemia.

Van Hove JL, Chace DH, Kahler SG, Millington DS. Van Hove JL, et al. Among authors: millington ds. J Inherit Metab Dis. 1993;16(2):361-7. doi: 10.1007/BF00710283. J Inherit Metab Dis. 1993. PMID: 8411998

5

Glycine and L-carnitine therapy in 3-methylcrotonyl-CoA carboxylase deficiency.

Rutledge SL, Berry GT, Stanley CA, van Hove JL, Millington D. Rutledge SL, et al. J Inherit Metab Dis. 1995;18(3):299-305. doi: 10.1007/BF00710419. J Inherit Metab Dis. 1995. PMID: 7474896

6

3-Hydroxyisovalerylcarnitine in 3-methylcrotonyl-CoA carboxylase deficiency.

van Hove JL, Rutledge SL, Nada MA, Kahler SG, Millington DS. van Hove JL, et al. Among authors: millington ds. J Inherit Metab Dis. 1995;18(5):592-601. doi: 10.1007/BF02436004. J Inherit Metab Dis. 1995. PMID: 8598640

7

Tandem mass spectrometry: a new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism.

Millington DS, Kodo N, Norwood DL, Roe CR. Millington DS, et al. J Inherit Metab Dis. 1990;13(3):321-4. doi: 10.1007/BF01799385. J Inherit Metab Dis. 1990. PMID: 2122093 No abstract available.

8

Identification of phenylpropionylcarnitine, a new metabolite of phenylpropionic acid, in a patient with medium chain acyl-CoA dehydrogenase deficiency.

Moore R, Millington DS, Norwood D, Kodo N, Robinson P, Glasgow JF. Moore R, et al. Among authors: millington ds. J Inherit Metab Dis. 1990;13(3):325-9. doi: 10.1007/BF01799386. J Inherit Metab Dis. 1990. PMID: 2122094 No abstract available.

9

Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiency.

Bennett MJ, Coates PM, Hale DE, Millington DS, Pollitt RJ, Rinaldo P, Roe CR, Tanaka K. Bennett MJ, et al. Among authors: millington ds. J Inherit Metab Dis. 1990;13(5):707-15. doi: 10.1007/BF01799572. J Inherit Metab Dis. 1990. PMID: 2246856

10

Variations in IBD (ACAD8) in children with elevated C4-carnitine detected by tandem mass spectrometry newborn screening.

Pedersen CB, Bischoff C, Christensen E, Simonsen H, Lund AM, Young SP, Koeberl DD, Millington DS, Roe CR, Roe DS, Wanders RJ, Ruiter JP, Keppen LD, Stein Q, Knudsen I, Gregersen N, Andresen BS. Pedersen CB, et al. Among authors: millington ds. Pediatr Res. 2006 Sep;60(3):315-20. doi: 10.1203/01.pdr.0000233085.72522.04. Epub 2006 Jul 20. Pediatr Res. 2006. PMID: 16857760

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