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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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428 -432
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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Tatuch, Y, Christodoulou, J, Feigenbaum, A, Clarke, JT, Wherret, J, Smith, C, Rudd, N, Petrova-Benedict, R, Robinson, BH.
Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high..
Am J Hum Genet
50(4)
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852 -858
1992
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Christodoulou, J, Mclnnes, RR.
Hereditary metabolic disease in infancy.
Current Opinion in Pediatrics
4(2)
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228 -240
1992
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Chow, CW, Poulos, A, Fellenberg, AJ, Christodoulou, J, Danks, DM.
Autopsy findings in two siblings with infantile Refsum disease..
Acta Neuropathol
83(2)
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190 -195
1992
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