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Christodoulou, J, McInnes, RR, Jay, V, Wilson, G, Becker, LE, Lehotay, DC, Platt, BA, Bridge, PJ, Robinson, BH, Clarke, JT.
Barth syndrome: clinical observations and genetic linkage studies..
Am J Med Genet
50(3)
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255 -264
1994
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Christodoulou, J, Kure, S, Hayasaka, K, Clarke, JT.
Atypical nonketotic hyperglycinemia confirmed by assay of the glycine cleavage system in lymphoblasts..
J Pediatr
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1993
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Christodoulou, J, Clarke, JT, Rupar, CA, Gordon, BA, Kelly, DP.
Retrospective diagnosis of medium chain acyl-CoA dehydrogenase deficiency..
J Paediatr Child Health
29(3)
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1993
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Christodoulou, J, Petrova-Benedict, R, Robinson, BH, Jay, V, Clarke, JT.
An unusual patient with the neonatal Marfan phenotype and mitochondrial complex I deficiency..
Eur J Pediatr
152(5)
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1993
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Christodoulou, J, Qureshi, IA, McInnes, RR, Clarke, JT.
Ornithine transcarbamylase deficiency presenting with strokelike episodes..
J Pediatr
122(3)
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423 -425
1993
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