Hargreaves I - Search Results

1

Assessment of mitochondrial respiratory chain function in hyperphenylalaninaemia.

Kyprianou N, Murphy E, Lee P, Hargreaves I. Kyprianou N, et al. Among authors: hargreaves i. J Inherit Metab Dis. 2009 Apr;32(2):289-96. doi: 10.1007/s10545-009-1080-5. Epub 2009 Mar 13. J Inherit Metab Dis. 2009. PMID: 19277893

2

Blood mononuclear cell coenzyme Q10 concentration and mitochondrial respiratory chain succinate cytochrome-c reductase activity in phenylketonuric patients.

Hargreaves IP, Heales SJ, Briddon A, Land JM, Lee PJ. Hargreaves IP, et al. J Inherit Metab Dis. 2002 Dec;25(8):673-9. doi: 10.1023/a:1022881231253. J Inherit Metab Dis. 2002. PMID: 12705497 Clinical Trial.

3

Assessment of mitochondrial electron transport chain function in a primary astrocyte cell model of hyperhomocystinaemia.

Turkes F, Murphy E, Land J, Demiray B, Duberley K, Briddon A, Hargreaves I. Turkes F, et al. Among authors: hargreaves i. Toxicol Mech Methods. 2013 Jul;23(6):459-63. doi: 10.3109/15376516.2013.780276. Epub 2013 Apr 17. Toxicol Mech Methods. 2013. PMID: 23464834

4

Primary pyruvate dehydrogenase E3 binding protein deficiency with mild hyperlactataemia and hyperalaninaemia.

Hargreaves IP, Heales SJ, Briddon A, Lee PJ, Hanna MG, Land JM. Hargreaves IP, et al. J Inherit Metab Dis. 2003;26(5):505-6. doi: 10.1023/a:1025181512847. J Inherit Metab Dis. 2003. PMID: 14518830

5

Human neuronal coenzyme Q10 deficiency results in global loss of mitochondrial respiratory chain activity, increased mitochondrial oxidative stress and reversal of ATP synthase activity: implications for pathogenesis and treatment.

Duberley KE, Abramov AY, Chalasani A, Heales SJ, Rahman S, Hargreaves IP. Duberley KE, et al. J Inherit Metab Dis. 2013 Jan;36(1):63-73. doi: 10.1007/s10545-012-9511-0. Epub 2012 Jul 6. J Inherit Metab Dis. 2013. PMID: 22767283

6

Mitochondrial cytochrome c release: a factor to consider in mitochondrial disease?

Oppenheim ML, Hargreaves IP, Pope S, Land JM, Heales SJ. Oppenheim ML, et al. Among authors: hargreaves ip. J Inherit Metab Dis. 2009 Apr;32(2):269-73. doi: 10.1007/s10545-009-1061-8. Epub 2009 Jan 26. J Inherit Metab Dis. 2009. PMID: 19169843

7

Homocysteine and cysteine - albumin binding in homocystinuria: assessment of cysteine status and implications for glutathione synthesis?

Hargreaves IP, Lee PJ, Briddon A. Hargreaves IP, et al. Amino Acids. 2002;22(2):109-18. doi: 10.1007/s007260200000. Amino Acids. 2002. PMID: 12395179

8

Glutathione deficiency in patients with mitochondrial disease: implications for pathogenesis and treatment.

Hargreaves IP, Sheena Y, Land JM, Heales SJ. Hargreaves IP, et al. J Inherit Metab Dis. 2005;28(1):81-8. doi: 10.1007/s10545-005-4160-1. J Inherit Metab Dis. 2005. PMID: 15702408

9

Mitochondrial respiratory chain defects are not accompanied by an increase in the activities of lactate dehydrogenase or manganese superoxide dismutase in paediatric skeletal muscle biopsies.

Hargreaves IP, Heales SJ, Land JM. Hargreaves IP, et al. J Inherit Metab Dis. 1999 Dec;22(8):925-31. doi: 10.1023/a:1005643508075. J Inherit Metab Dis. 1999. PMID: 10604144

10

Bezafibrate induced increase in mitochondrial electron transport chain complex IV activity in human astrocytoma cells: Implications for mitochondrial cytopathies and neurodegenerative diseases.

Ioannou N, Hargreaves IP, Allen G, Duberley K, Land JM, Heales SJ. Ioannou N, et al. Biofactors. 2010 Nov-Dec;36(6):468-73. doi: 10.1002/biof.120. Epub 2010 Sep 24. Biofactors. 2010. PMID: 20872762

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