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Urine heteroplasmy is the best predictor of clinical outcome in the m.3243A>G mtDNA mutation
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A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism
Keogh, Michael J., Daud, D., Pyle, A., Duff, J., Griffin, H., He, L., Alston, C. L., Steele, H., Taggart, S., Basu, A. P., Taylor, R. W., Horvath, R., Ramesh, V., Chinnery, Patrick F.
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Australian farm work injuries: incidence, diversity and personal risk factors
Low, J M, Griffith, G R, Alston, C L
Published in The Australian journal of rural health (01.08.1996)
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Transdimensional sequential Monte Carlo using variational Bayes — SMCVB
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Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions
Alston, Charlotte L, Schaefer, Andrew M, Raman, Pravrutha, Solaroli, Nicola, Krishnan, Kim J, Blakely, Emma L, He, Langping, Craig, Kate, Roberts, Mark, Vyas, Aashish, Nixon, John, Horvath, Rita, Turnbull, Douglass M, Karlsson, Anna, Gorman, Grainne S, Taylor, Robert W
Published in Neurology (03.12.2013)
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Changes in maintenance energy requirements of mature sheep fed at different levels of feed intake at maintenance, during weight loss and realimentation
Ball, A.J., Thompson, J.M., Alston, C.L., Blakely, A.R., Hinch, G.N.
Published in Livestock production science (01.03.1998)
Published in Livestock production science (01.03.1998)
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