Millington DS - Search Results

1

Benzoate therapy and carnitine deficiency in non-ketotic hyperglycinemia.

Van Hove JL, Kishnani P, Muenzer J, Wenstrup RJ, Summar ML, Brummond MR, Lachiewicz AM, Millington DS, Kahler SG. Van Hove JL, et al. Among authors: millington ds. Am J Med Genet. 1995 Dec 4;59(4):444-53. doi: 10.1002/ajmg.1320590410. Am J Med Genet. 1995. PMID: 8585564

2

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

3

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

4

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood.

Van Hove JL, Zhang W, Kahler SG, Roe CR, Chen YT, Terada N, Chace DH, Iafolla AK, Ding JH, Millington DS. Van Hove JL, et al. Among authors: millington ds. Am J Hum Genet. 1993 May;52(5):958-66. Am J Hum Genet. 1993. PMID: 8488845 Free PMC article.

5

Treatment of pyruvate carboxylase deficiency with high doses of citrate and aspartate.

Ahmad A, Kahler SG, Kishnani PS, Artigas-Lopez M, Pappu AS, Steiner R, Millington DS, Van Hove JL. Ahmad A, et al. Among authors: millington ds. Am J Med Genet. 1999 Dec 3;87(4):331-8. doi: 10.1002/(sici)1096-8628(19991203)87:4<331::aid-ajmg10>3.0.co;2-k. Am J Med Genet. 1999. PMID: 10588840

6

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

7

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

8

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.

9

L-carnitine therapy in isovaleric acidemia.

Roe CR, Millington DS, Maltby DA, Kahler SG, Bohan TP. Roe CR, et al. Among authors: millington ds. J Clin Invest. 1984 Dec;74(6):2290-5. doi: 10.1172/JCI111657. J Clin Invest. 1984. PMID: 6549017 Free PMC article.

10

Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders.

Shen JJ, Matern D, Millington DS, Hillman S, Feezor MD, Bennett MJ, Qumsiyeh M, Kahler SG, Chen YT, Van Hove JL. Shen JJ, et al. Among authors: millington ds. J Inherit Metab Dis. 2000 Feb;23(1):27-44. doi: 10.1023/a:1005694712583. J Inherit Metab Dis. 2000. PMID: 10682306

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