Land J - Search Results

1

Cytochrome c oxidase deficiency associated with the first stop-codon point mutation in human mtDNA.

Hanna MG, Nelson IP, Rahman S, Lane RJ, Land J, Heales S, Cooper MJ, Schapira AH, Morgan-Hughes JA, Wood NW. Hanna MG, et al. Among authors: land j. Am J Hum Genet. 1998 Jul;63(1):29-36. doi: 10.1086/301910. Am J Hum Genet. 1998. PMID: 9634511 Free PMC article.

2

Mitochondrial disease: a historical, biochemical, and London perspective.

Land JM, Morgan-Hughes JA, Hargreaves I, Heales SJ. Land JM, et al. Neurochem Res. 2004 Mar;29(3):483-91. doi: 10.1023/b:nere.0000014819.53972.b0. Neurochem Res. 2004. PMID: 15038596 Review.

3

Phenotypic variability of mitochondrial disease caused by a nuclear mutation in complex II.

Pagnamenta AT, Hargreaves IP, Duncan AJ, Taanman JW, Heales SJ, Land JM, Bitner-Glindzicz M, Leonard JV, Rahman S. Pagnamenta AT, et al. Among authors: land jm. Mol Genet Metab. 2006 Nov;89(3):214-21. doi: 10.1016/j.ymgme.2006.05.003. Epub 2006 Jun 23. Mol Genet Metab. 2006. PMID: 16798039

4

A new perspective on the treatment of aromatic L-amino acid decarboxylase deficiency.

Allen GF, Land JM, Heales SJ. Allen GF, et al. Among authors: land jm. Mol Genet Metab. 2009 May;97(1):6-14. doi: 10.1016/j.ymgme.2009.01.010. Epub 2009 Jan 27. Mol Genet Metab. 2009. PMID: 19231266 Review.

5

Decreased ubiquinone availability and impaired mitochondrial cytochrome oxidase activity associated with statin treatment.

Duncan AJ, Hargreaves IP, Damian MS, Land JM, Heales SJ. Duncan AJ, et al. Among authors: land jm. Toxicol Mech Methods. 2009 Jan;19(1):44-50. doi: 10.1080/15376510802305047. Toxicol Mech Methods. 2009. PMID: 19778232

6

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. Among authors: land jm. J Inherit Metab Dis. 1999 Dec;22(8):925-31. doi: 10.1023/a:1005643508075. J Inherit Metab Dis. 1999. PMID: 10604144

7

Diagnostic value of succinate ubiquinone reductase activity in the identification of patients with mitochondrial DNA depletion.

Hargreaves P, Rahman S, Guthrie P, Taanman JW, Leonard JV, Land JM, Heales SJ. Hargreaves P, et al. Among authors: land jm. J Inherit Metab Dis. 2002 Feb;25(1):7-16. doi: 10.1023/a:1015104910239. J Inherit Metab Dis. 2002. PMID: 12004863

8

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. Among authors: land jm. J Inherit Metab Dis. 2003;26(5):505-6. doi: 10.1023/a:1025181512847. J Inherit Metab Dis. 2003. PMID: 14518830

9

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

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

10

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: land jm. 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

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