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Worthington, S, Christodoulou, J, Wilcken, B, Peat, B.
Pregnancy and argininosuccinic aciduria..
J Inherit Metab Dis
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1996
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Tümer, Z, Horn, N, Tønnesen, T, Christodoulou, J, Clarke, JT, Sarkar, B.
Early copper-histidine treatment for Menkes disease..
Nat Genet
12(1)
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1996
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Poulos, A, Christodoulou, J, Chow, CW, Goldblatt, J, Paton, BC, Orii, T, Suzuki, Y, Shimozawa, N.
Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group..
J Pediatr
127(4)
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1995
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Smooker, PM, Christodoulou, J, McInnes, RR, Cotton, RG.
A mutation causing DHPR deficiency results in a frameshift and a secondary splicing defect..
J Med Genet
32(3)
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1995
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Christodoulou, J, Hoare, J, Hammond, J, Ip, WC, Wilcken, B.
Neonatal onset of medium-chain acyl-coenzyme A dehydrogenase deficiency with confusing biochemical features..
J Pediatr
126(1)
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1995
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