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White, SL, Thorburn, DR, Christodoulou, J, Dahl, HH.
Novel Mitochondrial DNA Variant That May Give a False Positive Diagnosis for the T8993C Mutation..
Mol Diagn
3(2)
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113 -117
1998
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Williams, AJ, Coakley, J, Christodoulou, J.
Automated analysis of mitochondrial enzymes in cultured skin fibroblasts..
Anal Biochem
259(2)
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176 -180
1998
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Christodoulou, J, Danks, DM, Sarkar, B, Baerlocher, KE, Casey, R, Horn, N, Tümer, Z, Clarke, JT.
Early treatment of Menkes disease with parenteral copper-histidine: long-term follow-up of four treated patients..
Am J Med Genet
76(2)
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154 -164
1998
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Ellaway, C, North, K, Arbuckle, S, Christodoulou, J.
Complex I deficiency in association with structural abnormalities of the diaphragm and brain..
J Inherit Metab Dis
21(1)
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72 -73
1998
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Ellaway, C, Christodoulou, J, Kamath, R, Carpenter, K, Wilcken, B.
The association of protein-losing enteropathy with cobalamin C defect..
J Inherit Metab Dis
21(1)
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17 -22
1998
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