Simon Williams

Using a large international sample to investigate epilepsy in Rett syndrome

H. Leonard, J. Downs, Kingsley Wong, 2013, Developmental medicine and child neurology.

The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy

Meredith Wilson, J. Christodoulou, H. Leonard, 2012, European Journal of Human Genetics.

Functional abilities in children and adults with the CDKL5 disorder

J. Christodoulou, H. Leonard, N. de Klerk, 2016, American journal of medical genetics. Part A.

Seizure variables and their relationship to genotype and functional abilities in the CDKL5 disorder

J. Christodoulou, H. Leonard, N. de Klerk, 2016, Neurology.

There is variability in the attainment of developmental milestones in the CDKL5 disorder

J. Christodoulou, H. Leonard, N. de Klerk, 2015, Journal of Neurodevelopmental Disorders.

Resourceful and creative methods are necessary to research rare disorders

H. Leonard, J. Downs, Kingsley Wong, 2013, Developmental medicine and child neurology.

Stereotypical hand movements in 144 subjects with Rett syndrome from the population‐based Australian database

W. Kaufmann, H. Leonard, P. Jacoby, 2010, Movement disorders : official journal of the Movement Disorder Society.

There is variability in the attainment of developmental milestones in the CDKL5 disorder

J. Christodoulou, H. Leonard, G. Ho, 2015, Journal of Neurodevelopmental Disorders.

Delineation of large deletions of the MECP2 gene in Rett syndrome patients, including a familial case with a male proband

Robert L L Smith, S. Hardwick, J. Christodoulou, 2007, European Journal of Human Genetics.