-
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)
:
596 -599
1995
view publication
-
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)
:
220 -223
1995
view publication
-
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)
:
65 -68
1995
view publication
-
Ozand, PT, Nyhan, WL, al Aqeel, A, Christodoulou, J.
Malonic aciduria..
Brain Dev
16 Suppl:
7 -11
1994
view publication
-
Tein, I, Christodoulou, J, Donner, E, McInnes, RR.
Carnitine palmitoyltransferase II deficiency: a new cause of recurrent pancreatitis..
J Pediatr
124(6)
:
938 -940
1994
view publication