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Williams, AJ, Coakley, JC, Christodoulou, J.
Automated quantitation of total protein in cultured skin fibroblasts..
Clin Chim Acta
259(1-2)
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129 -136
1997
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Walker, DC, Christodoulou, J, Craig, HJ, Simard, LR, Ploder, L, Howell, PL, McInnes, RR.
Intragenic complementation at the human argininosuccinate lyase locus. Identification of the major complementing alleles..
J Biol Chem
272(10)
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6777 -6783
1997
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Freckmann, ML, Thorburn, DR, Kirby, DM, Kamath, KR, Hammond, J, Dennett, X, Christodoulou, J.
Mitochondrial electron transport chain defect presenting as hypoglycemia..
J Pediatr
130(3)
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431 -436
1997
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Ogle, RF, Christodoulou, J, Fagan, E, Blok, RB, Kirby, DM, Seller, KL, Dahl, HH, Thorburn, DR.
Mitochondrial myopathy with tRNA(Leu(UUR)) mutation and complex I deficiency responsive to riboflavin..
J Pediatr
130(1)
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138 -145
1997
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Christodoulou, J, Teo, SH, Hammond, J, Sim, KG, Hsu, BY, Stanley, CA, Watson, B, Lau, KC, Wilcken, B.
First prenatal diagnosis of the carnitine transporter defect..
Am J Med Genet
66(1)
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21 -24
1996
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