-
ELLAWAY, C, ELLIOTT, E, CHRISTODOULOU, J. Progressive myoclonic epilepsies: Recent genetic advances.
Journal of Paediatrics and Child Health
33(2)
:
91 -95
1997
view publication
-
Menezes, MJ, Menezes, MP, Riley, L, Cooper, S, Christodoulou, J. The need for careful diagnosis of congenital myasthenic syndromes with secondary complex I disorders.
Mitochondrion
13(6)
:
906
2013
view publication
-
Williamson, SL, Ellaway, CJ, Peters, GB, Pelka, GJ, Tam, PP, Christodoulou, J. Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotype.
European Journal of Human Genetics
23(9)
:
1171 -1175
2014
view publication
-
Christodoulou, J, McInnes, RR, Jay, V, Wilson, G, Becker, LE, Lehotay, DC, Platt, B, Bridge, PJ, Robinson, BH, Clarke, JTR. Barth syndrome: Clinical observations and genetic linkage studies.
American Journal of Medical Genetics
50(3)
:
255 -264
1994
view publication
-
Fehr, S, Leonard, H, Ho, G, Williams, S, de Klerk, N, Forbes, D, Christodoulou, J, Downs, J. There is variability in the attainment of developmental milestones in the CDKL5 disorder.
Journal of Neurodevelopmental Disorders
7(1)
:
2
2015
view publication