Bartlett K - Search Results

1

Lipid storage myopathy associated with low acyl-CoA dehydrogenase activities.

Turnbull DM, Shepherd IM, Ashworth B, Bartlett K, Johnson MA, Cullen MJ, Jackson S, Sherratt HS. Turnbull DM, et al. Among authors: bartlett k. Brain. 1988 Aug;111 ( Pt 4):815-28. doi: 10.1093/brain/111.4.815. Brain. 1988. PMID: 3042086

2

Very long-chain acyl coenzyme A dehydrogenase deficiency presenting with exercise-induced myoglobinuria.

Ogilvie I, Pourfarzam M, Jackson S, Stockdale C, Bartlett K, Turnbull DM. Ogilvie I, et al. Among authors: bartlett k. Neurology. 1994 Mar;44(3 Pt 1):467-73. doi: 10.1212/wnl.44.3_part_1.467. Neurology. 1994. PMID: 8145917

3

Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy.

Turnbull DM, Bartlett K, Eyre JA, Gardner-Medwin D, Johnson MA, Fisher J, Watmough NJ. Turnbull DM, et al. Among authors: bartlett k. Dev Med Child Neurol. 1988 Oct;30(5):667-72. doi: 10.1111/j.1469-8749.1988.tb04806.x. Dev Med Child Neurol. 1988. PMID: 3229565

4

Measurement of acyl-CoA dehydrogenase activity in cultured skin fibroblasts and blood platelets.

Taylor RW, Jackson S, Pourfarzam M, Bartlett K, Turnbull DM. Taylor RW, et al. Among authors: bartlett k. J Inherit Metab Dis. 1992;15(5):727-32. doi: 10.1007/BF01800014. J Inherit Metab Dis. 1992. PMID: 1434512

5

Quantitation of acyl-CoA and acylcarnitine esters accumulated during abnormal mitochondrial fatty acid oxidation.

Kler RS, Jackson S, Bartlett K, Bindoff LA, Eaton S, Pourfarzam M, Frerman FE, Goodman SI, Watmough NJ, Turnbull DM. Kler RS, et al. Among authors: bartlett k. J Biol Chem. 1991 Dec 5;266(34):22932-8. J Biol Chem. 1991. PMID: 1744086 Free article.

6

Immunoreactive enzyme protein in medium-chain acyl-CoA dehydrogenase deficiency.

Ogilvie I, Jackson S, Bartlett K, Turnbull DM. Ogilvie I, et al. Among authors: bartlett k. Biochem Med Metab Biol. 1991 Dec;46(3):373-9. doi: 10.1016/0885-4505(91)90085-y. Biochem Med Metab Biol. 1991. PMID: 1793614

7

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Jackson S, Bartlett K, Land J, Moxon ER, Pollitt RJ, Leonard JV, Turnbull DM. Jackson S, et al. Among authors: bartlett k. Pediatr Res. 1991 Apr;29(4 Pt 1):406-11. doi: 10.1203/00006450-199104000-00016. Pediatr Res. 1991. PMID: 1830138 Free article.

8

Short-chain acyl-CoA dehydrogenase deficiency.

Turnbull DM, Shepherd IM, Bartlett K, Sherratt HS. Turnbull DM, et al. Among authors: bartlett k. Prog Clin Biol Res. 1990;321:313-24. Prog Clin Biol Res. 1990. PMID: 2326296 No abstract available.

9

Measurement of the acyl-CoA intermediates of beta-oxidation by h.p.l.c. with on-line radiochemical and photodiode-array detection. Application to the study of [U-14C]hexadecanoate oxidation by intact rat liver mitochondria.

Watmough NJ, Turnbull DM, Sherratt HS, Bartlett K. Watmough NJ, et al. Among authors: bartlett k. Biochem J. 1989 Aug 15;262(1):261-9. doi: 10.1042/bj2620261. Biochem J. 1989. PMID: 2818568 Free PMC article.

10

Defects of fatty acid oxidation in skeletal muscle.

Turnbull DM, Bartlett K, Watmough NJ, Shepherd IM, Sherratt HS. Turnbull DM, et al. Among authors: bartlett k. J Inherit Metab Dis. 1987;10 Suppl 1:105-12. doi: 10.1007/BF01812851. J Inherit Metab Dis. 1987. PMID: 3119934 Review.

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