Millington D - Search Results

1

2-Methylbutyryl-coenzyme A dehydrogenase deficiency: a new inborn error of L-isoleucine metabolism.

Gibson KM, Burlingame TG, Hogema B, Jakobs C, Schutgens RB, Millington D, Roe CR, Roe DS, Sweetman L, Steiner RD, Linck L, Pohowalla P, Sacks M, Kiss D, Rinaldo P, Vockley J. Gibson KM, et al. Among authors: millington d. Pediatr Res. 2000 Jun;47(6):830-3. doi: 10.1203/00006450-200006000-00025. Pediatr Res. 2000. PMID: 10832746

2

Intravenous L-carnitine and acetyl-L-carnitine in medium-chain acyl-coenzyme A dehydrogenase deficiency and isovaleric acidemia.

Van Hove JL, Kahler SG, Millington DS, Roe DS, Chace DH, Heales SJ, Roe CR. Van Hove JL, et al. Among authors: millington ds. Pediatr Res. 1994 Jan;35(1):96-101. doi: 10.1203/00006450-199401000-00020. Pediatr Res. 1994. PMID: 8134205

3

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.

4

Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening.

Koeberl DD, Young SP, Gregersen NS, Vockley J, Smith WE, Benjamin DK Jr, An Y, Weavil SD, Chaing SH, Bali D, McDonald MT, Kishnani PS, Chen YT, Millington DS. Koeberl DD, et al. Among authors: millington ds. Pediatr Res. 2003 Aug;54(2):219-23. doi: 10.1203/01.PDR.0000074972.36356.89. Epub 2003 May 7. Pediatr Res. 2003. PMID: 12736383

5

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

6

Diagnostic and therapeutic implications of medium-chain acylcarnitines in the medium-chain acyl-coA dehydrogenase deficiency.

Roe CR, Millington DS, Maltby DA, Bohan TP, Kahler SG, Chalmers RA. Roe CR, et al. Among authors: millington ds. Pediatr Res. 1985 May;19(5):459-66. doi: 10.1203/00006450-198505000-00011. Pediatr Res. 1985. PMID: 4000772

7

2,4-Dienoyl-coenzyme A reductase deficiency: a possible new disorder of fatty acid oxidation.

Roe CR, Millington DS, Norwood DL, Kodo N, Sprecher H, Mohammed BS, Nada M, Schulz H, McVie R. Roe CR, et al. Among authors: millington ds. J Clin Invest. 1990 May;85(5):1703-7. doi: 10.1172/JCI114624. J Clin Invest. 1990. PMID: 2332510 Free PMC article.

8

Identification of 3-methylglutarylcarnitine. A new diagnostic metabolite of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.

Roe CR, Millington DS, Maltby DA. Roe CR, et al. Among authors: millington ds. J Clin Invest. 1986 Apr;77(4):1391-4. doi: 10.1172/JCI112446. J Clin Invest. 1986. PMID: 3958190 Free PMC article.

9

Carnitine homeostasis in the organic acidurias.

Roe CR, Millington DS, Kahler SG, Kodo N, Norwood DL. Roe CR, et al. Among authors: millington ds. Prog Clin Biol Res. 1990;321:383-402. Prog Clin Biol Res. 1990. PMID: 2183238 Review.

10

Medium-chain acyl-CoA dehydrogenase deficiency.

Millington DS, Roe CR. Millington DS, et al. N Engl J Med. 1989 May 4;320(18):1219. doi: 10.1056/NEJM198905043201817. N Engl J Med. 1989. PMID: 2710197 No abstract available.

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